Molecular hydrogen is a promising therapeutic agent for pulmonary disease

Molecular hydrogen is a promising therapeutic agent for pulmonary disease 分子氢——一种具有广泛应用前景的肺部疾病治疗剂 first-author corresp Jin ZHANG, zhangjin11170@163.com Jin ZHANG, zhangjin11170@163.com zhangjin11170@163.com https://orcid.org/0000-0003-4495-4212 Department of Anesthesiology, Shengjing Hospital of China Medical University, Shenyang 110004, China Department of Anesthesiology, Shengjing Hospital of China Medical University, Shenyang 110004, China Molecular hydrogen exerts biological effects on nearly all organs. It has anti-oxidative, anti-inflammatory, and anti-aging effects and contributes to the regulation of autophagy and cell death. As the primary organ for gas exchange, the lungs are constantly exposed to various harmful environmental irritants. Short- or long-term exposure to these harmful substances often results in lung injury, causing respiratory and lung diseases. Acute and chronic respiratory diseases have high rates of morbidity and mortality and have become a major public health concern worldwide. For example, coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has become a global pandemic. An increasing number of studies have revealed that hydrogen may protect the lungs from diverse diseases, including acute lung injury, chronic obstructive pulmonary disease, asthma, lung cancer, pulmonary arterial hypertension, and pulmonary fibrosis. In this review, we highlight the multiple functions of hydrogen and the mechanisms underlying its protective effects in various lung diseases, with a focus on its roles in disease pathogenesis and clinical significance. 氢有多种生物学功能，在各种肺部疾病中有重要的保护作用，在临床中有广泛的应用前景。本综述基于截至2021年5月的出版物，通过PubMed数据库中的选择性搜索检索，包括临床试验、动物研究和综述，搜索词包括“氢”“急性肺损伤”“慢性阻塞性肺疾病”“哮喘”“癌症”“肺病”，探讨了分子氢的作用机制及其对生物功能和细胞过程的影响，概述其对各种肺部疾病的研究现状，为基于分子氢的未来治疗方法的发展提供了理论支持。 Molecular hydrogen Pulmonary disease Reactive oxygen species (ROS) Oxidative stress Inflammation 分子氢 肺部疾病 活性氧（ROS） 氧化应激 炎症 1 Introduction 1 Molecular hydrogen is a colorless, odorless, and tasteless gas molecule with poor water solubility. It is considered inert in mammalian cells under physiological conditions. Molecular hydrogen can be broken down by some bacteria via enzymatic catalysis to provide energy and electrons. In addition, bacteria produce molecular hydrogen by anaerobic metabolism. Genes encoding the iron- or nickel-containing enzymes necessary to catalyze these reactions, such as hydrogenase, are lacking in mammals ( Fritsch et al., 2013 Fritsch et al., 2013 ). However, molecular hydrogen is now recognized as a novel medically relevant gas with therapeutic potential. Ohsawa et al. (2007) Ohsawa et al. (2007) reported that the inhalation of 2% molecular hydrogen results in the selective scavenging of hydroxyl free radical (·OH) and peroxynitrite anion (ONOO - ), significantly improving oxidative stress injury caused by cerebral ischemia/reperfusion (I/R). This study prompted substantial interest in the medical value of molecular hydrogen, and many cellular, animal, and clinical trials and studies have since investigated its preventive and therapeutic effects. Molecular hydrogen can exert biological effects on almost all organs, including the brain, heart, lung, liver, and pancreas. It has a variety of biological functions, including roles in the regulation of oxidative stress and anti-inflammatory and anti-apoptotic effects ( Iketani and Ohsawa, 2017 Iketani and Ohsawa, 2017 ; Kura et al., 2019 Kura et al., 2019 ; Hu et al., 2020 Hu et al., 2020 ; Kawamura T et al., 2020 Kawamura T et al., 2020 ). The lungs are the primary organ for gas exchange between the surrounding environment and the circulatory system. During respiration, they are constantly exposed to various environmental irritants, such as bacteria, viruses, and other pathogens, and to other harmful external stimuli, such as tobacco smoke and airborne particulate matter. Short- or long-term exposure to these harmful substances often results in lung injury, causing respiratory and lung diseases ( Bhattacharya and Matthay, 2013 Bhattacharya and Matthay, 2013 ). Acute and chronic respiratory diseases have high rates of morbidity and mortality, and the efficacy of treatment strategies is insufficient, making these diseases a major public health concern worldwide ( Bhattacharya and Matthay, 2013 Bhattacharya and Matthay, 2013 ). For example, coronavirus disease 2019 (COVID-19), a form of pneumonia caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has spread widely, resulting in an ongoing pandemic. This review is based on publications up to May 2021 which were retrieved by a selective search in the PubMed database, and includes clinical trials, animal studies, and reviews. The search terms included "hydrogen," "acute lung injury (ALI)," "chronic obstructive pulmonary disease (COPD)," "asthma," "cancer," "pulmonary arterial hypertension (PAH)," "pulmonary fibrosis (PF)," and "hydrogen." We briefly discuss the mechanism of action of molecular hydrogen and its effects on biological functions and cellular processes. We then describe the status of research on its contributions to various lung diseases. We expect molecular hydrogen to have an increasing role in the treatment and prevention of lung diseases. This review provides support for the development of future treatments based on molecular hydrogen. 2 Mechanism of action of hydrogen 1 2.1 Anti-oxidation 2 Reactive oxygen species (ROS) and reactive nitrogen species (RNS) are by-products of energy metabolism during daily activities. ROS/RNS include superoxide anion (O 2 - ), ·OH, peroxyl (RO 2 ·), alkoxyl (RO·), and nitric oxide (NO·) radicals. They play critical roles under normal conditions in immune defense, signaling processes, and the extraction of energy from organic molecules ( Genestra, 2007 Genestra, 2007 ). However, if ROS and RNS production exceeds the antioxidant capacity of the body or if the antioxidant capacity of the body is decreased, oxidative stress occurs. Acute oxidative stress often occurs during inflammation and I/R (e.g., cardiac arrest, myocardial and cerebral infarction, organ transplantation, and intraoperative hemostasis) ( Ferrari et al., 1991 Ferrari et al., 1991 ; Vaziri and Rodríguez-Iturbe, 2006 Vaziri and Rodríguez-Iturbe, 2006 ; Reuter et al., 2010 Reuter et al., 2010 ). Chronic ROS injury can occur in a variety of pathological conditions, such as malignant cancer, diabetes, chronic inflammatory diseases, atherosclerosis, and neurodegeneration, as well as in the process of aging ( Stump et al., 2005 Stump et al., 2005 ; Kim and Byzova, 2014 Kim and Byzova, 2014 ; Guzik and Touyz, 2017 Guzik and Touyz, 2017 ). Humans have antioxidant defense systems to protect against free radical toxicity ( Birben et al., 2012 Birben et al., 2012 ). Antioxidants are divided into enzymatic and non-enzymatic types. Enzymatic types include superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GSH-Px), and non-enzymatic types include bilirubin, α‍-tocopherol (vitamin E), β‍-carotene, and uric acid ( Wu et al., 2013 Wu et al., 2013 ). The antioxidant effects of molecular hydrogen are primarily mediated by the following mechanisms. (1) Molecular hydrogen has a lower molecular weight than other common antioxidants (e.g., SOD, CAT, and α‍-tocopherol). It can selectively react with strong oxidants and can easily penetrate biological membranes, such as nuclear and mitochondrial membranes, without affecting the metabolic redox reaction ( Ohta, 2012 Ohta, 2012 , 2015 2015 ). (2) By stimulating nuclear factor erythroid 2-related factor 2 (Nrf2), which regulates the basal and induces expression of many antioxidant enzymes and the proteasome ( Zhang HQ et al., 2015 Zhang HQ et al., 2015 ), hydrogen can increase the expression of heme oxygenase-1 (HO-1) ( Kawamura et al., 2013 Kawamura et al., 2013 ; Xie et al., 2020 Xie et al., 2020 ; Yu et al., 2020 Yu et al., 2020 ). It also decreases ·ONOO - -related gene expression and production ( Shinbo et al., 2013 Shinbo et al., 2013 ) and increases the activity of the antioxidant enzymes SOD, CAT, and myeloperoxidase (MPO) ( Cai et al., 2013 Cai et al., 2013 ). (3) Molecular hydrogen can block the apoptosis signal-regulating kinase 1 (ASK1) signaling pathway and the downstream signaling molecule p38 mitogen-activated protein kinase (p38 MAPK ), thereby inhibiting nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activity and decreasing free radical production. Through these antioxidant effects, molecular hydrogen protects cells from lipid and fatty acid peroxidation. 2.2 Anti-inflammatory effects 2 The anti-inflammatory effects of molecular hydrogen were first identified in a study of Gharib et al. (2001) Gharib et al. (2001) in which parasite-induced liver inflammation was treated by the inhalation of high-pressure hydrogen. Subsequent studies of a variety of injury models have confirmed that molecular hydrogen has anti-inflammatory effects. In the lungs, acute and persistent chronic inflammation underlies the pathogenesis of numerous pulmonary diseases, such as ALI, COPD, asthma, and PF. The protective effect of molecular hydrogen on lung tissues is mediated by its anti-inflammatory effects. The major mechanisms underlying the anti-inflammatory effects of molecular hydrogen are as follows. (1) It inhibits the synthesis and release of the pro-inflammatory factors tumor necrosis factor-‍‍α (TNF-‍α), interleukin (IL)-‍‍‍1β, IL-6, nuclear factor-‍κB (NF-‍κB), and high-mobility group box 1 (HMGB-1); increases the expression of the anti-inflammatory factor IL-‍10 ( Buchholz et al., 2008 Buchholz et al., 2008 ; Shao et al., 2016 Shao et al., 2016 ; Fu et al., 2020 Fu et al., 2020 ); inhibits the release of chemokines, including keratinocyte-derived chemokine, macrophage inflammatory protein (MIP)-‍1α, MIP-2, and monocyte chemoattractant protein 1 ( Xie et al., 2012 Xie et al., 2012 ); and inhibits the release of intercellular cell adhesion molecule-1 (ICAM-1), granulocyte-macrophage colony-stimulating factor (GMCSF), and granulocyte colony-stimulating factor (G-CSF) ( Xie et al., 2012 Xie et al., 2012 ; Chen MH et al., 2018 Chen MH et al., 2018 ). (2) It promotes macrophage phagocytosis at lesion sites ( Huang et al., 2019 Huang et al., 2019 ) and inhibits the recruitment of neutrophils and M1 macrophages to lesions. (3) The anti-inflammatory effects of molecular hydrogen involve multiple signaling pathways. For example, the stimulation of the Nrf2/HO-1/HMGB-1 pathway mitigates endothelial dysfunction and lung injury caused by polymicrobial sepsis ( Chen et al., 2015 Chen et al., 2015 ; Yang et al., 2019 Yang et al., 2019 ). The inhibition of p38 MAPK and c-Jun N-terminal kinase (JNK) alleviates lipopolysaccharide (LPS)-induced ALI ( Tao et al., 2016 Tao et al., 2016 ). The modulation of autophagy-related pathways, such as the mammalian target of rapamycin (mTOR)/transcription factor EB (TFEB) and phosphatase and tensin homolog (PTEN)‍-induced kinase 1 (PINK1)/Parkin pathways, mitigates ALI endothelial dysfunction and myocardial I/R injury ( Chen et al., 2020 Chen et al., 2020 ; Fu et al., 2020 Fu et al., 2020 ). 2.3 Regulation of autophagy 2 In eukaryotic cells, catabolism is the degradation of intracellular components by the ubiquitin-proteasome system and lysosomes. Autophagy (particularly macro‍autophagy) is defined as a lysosome-dependent catabolic process for maintaining cellular homeostasis ( Yang and Klionsky, 2010 Yang and Klionsky, 2010 ). However, when stress exceeds a critical duration or intensity threshold, it may have maladaptive effects ( Maiuri et al., 2007 Maiuri et al., 2007 ), causing cell damage or even death. Emerging evidence suggests that hydrogen has dual roles in the modulation of autophagy (i.e., roles in both its promotion and inhibition). 2.3.1　Promotion of autophagy 3 Hydrogen can promote autophagy-mediated nucleotide-binding domain and leucine-rich repeat protein 3 (NLRP3) inactivation in macrophages and alleviate inflammatory reactions and subsequent organ damage and mitochondrial dysfunction ( Chen HG et al., 2019 Chen HG et al., 2019 ). In sepsis, endoplasmic reticulum (ER) stress is triggered and is often accompanied by impaired autophagy. Hydrogen alleviates ER stress by activating autophagy pathways, thereby attenuating inflammation and organ injury ( Chen et al., 2020 Chen et al., 2020 ). These observations suggest that under pathological conditions, as a key regulator of innate and adaptive immunity, autophagy is activated, but is not sufficient to overcome stress. Hydrogen exerts protective effects by promoting autophagy for the maintenance of homeostasis and attenuation of the effects of stress. 2.3.2　Inhibition of autophagy 3 Basal autophagy is essential for the maintenance of normal cellular functions and homeostasis. However, dysregulated or excessive autophagy may disrupt intracellular homeostasis, predisposing individuals to pathological conditions. Under these conditions, appropriate inhibition of autophagy serves a protective function. We have demonstrated that hydrogen alleviates LPS-induced ALI by inhibiting excessive autophagy ( Zhang Y et al., 2015 Zhang Y et al., 2015 ; Liu and Zhang, 2017 Liu and Zhang, 2017 ). Similarly, in traumatic brain injury, by inhibiting autophagy, hydrogen improves the viability of microvascular endothelial cells (ECs) ( Wang YF et al., 2020 Wang YF et al., 2020 ). The mechanisms underlying the dual effects of hydrogen on autophagy are yet to be fully clarified and might depend on disease stage or severity, as well as cell types and locations. Nevertheless, these findings suggest that hydrogen is a candidate therapeutic agent for the modulation of autophagy pathways and therefore, disease outcomes. 2.4 Effects of hydrogen on cell death 2 2.4.1　Regulation of apoptosis 3 Apoptosis is a canonical form of programmed cell death that does not stimulate inflammatory responses ( Elmore, 2007 Elmore, 2007 ). It is an evolutionarily conserved type of cell death with major effects on biological processes ( Singh et al., 2019 Singh et al., 2019 ). The molecular mechanism underlying apoptosis involves the sequential activation of cysteine proteases, called caspases ( Shalini et al., 2015 Shalini et al., 2015 ), and a series of pro-apoptotic and anti-apoptotic B-cell lymphoma-2 (Bcl-2) family proteins ( Westphal et al., 2014 Westphal et al., 2014 ). In various disease models and organs, molecular hydrogen plays a protective role by regulating apoptosis. It can inhibit apoptosis by regulating apoptosis signaling pathways and apoptosis-related proteins, such as the phosphatidylinositol-3-kinase (PI3K)/protein kinase B (Akt)/glycogen synthase kinase-3β (GSK3β) ( Chen et al., 2017 Chen et al., 2017 ), ASK1/JNK ( Liu YQ et al., 2015 Liu YQ et al., 2015 ), rat sarcoma (Ras)-extracellular signal-related kinase 1/2 (ERK1/2)-mitogen-activated protein kinase kinase 1/2 (MEK1/2), and Akt pathways ( Chen et al., 2013 Chen et al., 2013 ), and by suppressing the activation of caspase-3, -8, and -9 and the Bcl-2/Bcl-2-associated X (Bax) ratio ( Huo et al., 2014 Huo et al., 2014 ; Liu YQ et al., 2015 Liu YQ et al., 2015 ; Mo et al., 2019 Mo et al., 2019 ). Molecular hydrogen also reduces the rate of apoptosis by reducing inflammation and oxidative damage ( Guo SX et al., 2015 Guo SX et al., 2015 ; Li et al., 2016 Li et al., 2016 ), and protects mitochondrial function ( Cui et al., 2014 Cui et al., 2014 ; Jiao et al., 2020 Jiao et al., 2020 ). The inhibition of autophagy improves cell survival and inhibits apoptosis. For example, in an I/R myocardial injury model, PINK-mediated autophagy alleviates inflammation and apoptosis ( Yao et al., 2019 Yao et al., 2019 ). Accordingly, there is crosstalk among molecular hydrogen, apoptosis, and autophagy. Although hydrogen has anti-apoptotic effects in the above conditions, it promotes apoptosis under various other conditions. For example, hydrogen can increase rates of early and late apoptosis in lung cancer ( Jiang et al., 2018 Jiang et al., 2018 ; Wang et al., 2018 Wang et al., 2018 ). It facilitates the scavenging of carcinoma cells in body, reduces cell proliferation, and promotes cancer cell apoptosis. The mechanisms underlying the contrasting effects of hydrogen on apoptosis are not completely understood. However, they may be explained by the ability of hydrogen to modulate cell death via different pathways to protect against injury and other harmful attacks. 2.4.2　Regulation of pyroptosis 3 Pyroptosis is a novel form of programmed cell death associated with inflammation. The activation of pattern-recognition receptors (PRRs) in inflammasomes can trigger pyroptosis by stimulating inflammatory responses ( Guo HT et al., 2015 Guo HT et al., 2015 ; Shi et al., 2017 Shi et al., 2017 ). Pyroptosis is a protective mechanism, but excessive pyroptosis can have serious consequences. ROS and the activation of caspase-1 and inflammasomes play important roles in promoting pyroptosis ( Lamkanfi and Dixit, 2014 Lamkanfi and Dixit, 2014 ; Zha et al., 2016 Zha et al., 2016 ). Molecular hydrogen plays an important regulatory role in resistance to inflammation and oxidation. Thus, molecular hydrogen might affect pyroptosis in inflammatory diseases, such as sepsis and I/R injury. In a rat model of myocardial I/R injury, hydrogen inhibited oxidative stress and NLRP3-mediated pyroptosis and significantly improved cardiac function, microstructure, and mitochondrial morphology ( Nie et al., 2021 Nie et al., 2021 ). 2.5 Regulation of aging 2 Aging is a progressive loss of physiological function and is an unavoidable process ending in death ( Golden and Melov, 2007 Golden and Melov, 2007 ; Newgard and Sharpless, 2013 Newgard and Sharpless, 2013 ). It is now considered a major factor underlying the development and progression of various diseases, such as COPD and idiopathic PF. Molecular hydrogen can decrease the expression of the aging-related proteins β‍-galactosidase, p53, and p21 ( Han et al., 2017 Han et al., 2017 ; Zhang WB et al., 2018 Zhang WB et al., 2018 ), suppress downregulation of sirtuin 3 (Sirt3) expression, and reduce oxidative stress damage, thereby extending cell survival ( Li et al., 2019 Li et al., 2019 ; Zhang et al., 2020 Zhang et al., 2020 ). Research has shown that molecular hydrogen produced by intestinal bacteria in the body suppresses increased hydrogen peroxide (H 2 O 2 ) by suppressing intracellular ·OH-mediated lipid peroxide formation and cellular senescence, thus contributing to the suppression of aging ( Sakai et al., 2019 Sakai et al., 2019 ). Genomic instability is one of the primary hallmarks of the aging process ( Li et al., 2021 Li et al., 2021 ). By reducing oxidative DNA damage, hydrogen can help maintain genomic stability. For example, in cigarette smoke (CS)‍-induced emphysema, hydrogen significantly decreased phosphorylated histone H2AX and 8-hydroxy-2'-deoxyguanosine (8-OHdG), which are markers of oxidative DNA damage ( Suzuki et al., 2017 Suzuki et al., 2017 ). As a "philosophical molecule," hydrogen may be used for the treatment of intractable diseases and aging ( Hirano et al., 2020 Hirano et al., 2020 ). Some possible mechanisms underlying the biological effects of hydrogen are summarized in Fig. 1 Fig. 1 . 3 Protective function of molecular hydrogen in lung diseases 1 To understand the following text easily and fully explain the preventive and therapeutic effects of hydrogen in various lung diseases, we first summarize the extensive therapeutic spectrum of hydrogen in lung diseases in Fig. 2 Fig. 2 a. We describe the specific therapeutic effects of hydrogen in ALI in detail in Fig. 2 Fig. 2 b. 1;2; 3.1 Role of hydrogen in ALI 2 ALI and its more severe form, acute respiratory distress syndrome (ARDS), are characterized by an excessive inflammatory response in the lungs and severe gas exchange dysfunction due to disruption of the alveolar–capillary barrier and pulmonary edema. Although supportive critical care medicine has resulted in an increase in survival rates of ALI/ARDS in the past two decades, mortality rates remain high ( Goss et al., 2003 Goss et al., 2003 ; Maybauer et al., 2006 Maybauer et al., 2006 ). A variety of anti-inflammatory drugs have been studied to treat ALI. Palrnatine can inhibit the activation of the Akt/NF-‍κB signaling pathway, and relieve LPS-induced ALI in mice and in LPS-induced RAW264.7 cells ( Kan et al., 2021 Kan et al., 2021 ). Recent studies of animal models by our group and others have indicated that hydrogen has the potential to alleviate the pathogenesis of ALI caused by LPS, sepsis, and other pathogenic factors. 3.1.1　Effect of hydrogen on ALI caused by LPS 3 LPS, also known as endotoxin, is a component of the outer membrane of Gram-negative bacteria. Toll-like receptors (TLRs) are representative PRRs, which induce pro-inflammatory responses to pathogen invasion ( Fitzgerald and Kagan, 2020 Fitzgerald and Kagan, 2020 ). PRRs recognize evolutionarily conserved components in microorganisms, collectively called pathogen-associated molecular patterns (PAMPs). LPS is a PAMP and is recognized by TLR4, stimulating TLR4-dependent inflammatory responses and triggering the host innate immune system ( Akira and Hemmi, 2003 Akira and Hemmi, 2003 ; Tang et al., 2012 Tang et al., 2012 ). Many studies have shown that hydrogen can alleviate ALI caused by LPS, serving a protective function by the following major mechanisms. Hydrogen treatment can reduce the degree of inflammation in lung tissues, inhibit early and late NF-‍κB activation-mediated inflammation and pulmonary cell apoptosis, and markedly attenuate neutrophil recruitment caused by LPS. These protective effects are mediated by the downregulation of lung MPO activity and proinflammatory cytokines and chemokines ( Xie et al., 2012 Xie et al., 2012 ). Hydrogen significantly reduces p38 MAPK expression and activation ( Liang et al., 2012 Liang et al., 2012 ) and p38 MAPK -dependent ROS ( Shi et al., 2016 Shi et al., 2016 ; Tao et al., 2016 Tao et al., 2016 ). In addition to its good efficacy when used alone, hydrogen in combination with NO can provide enhanced therapeutic efficacy for LPS-induced ALI. The underlying mechanism may involve the interaction between these two gases, whereby the combination of NO with hydrogen eliminates nitrotyrosine caused by NO inhalation alone ( Liu HY et al., 2015 Liu HY et al., 2015 ). Hydrogen can reduce LPS-induced lung epithelial barrier dysfunction. Under normal conditions, the alveolar epithelium serves as an important barrier to prevent pulmonary edema. In mammalian airways, aquaporins (AQPs), a family of cell membrane transport proteins, play critical roles in airway fluid transport, humidification, and surface liquid hydration, and modulate water permeability in the lungs ( Bai et al., 1999 Bai et al., 1999 ; Song et al., 2000 Song et al., 2000 , 2001 2001 ). We have demonstrated that LPS significantly decreases AQP-1 and AQP-5 expression and causes barrier dysfunction in the lungs. Hydrogen-rich saline (HRS) significantly increases AQP-1 and AQP-5 expression and alleviates pulmonary epithelial cell damage, thereby protecting the pulmonary epithelial barrier function ( Liu et al., 2016 Liu et al., 2016 ; Tao et al., 2016 Tao et al., 2016 ). Hydrogen reduces LPS-induced endothelial dysfunction. Pulmonary microvascular endothelial cells (PMVECs) are primary targets in LPS-induced ALI. LPS causes PMVEC dysfunction, resulting in increased permeability of EC monolayers as well as EC shrinkage and death ( Lee and Slutsky, 2010 Lee and Slutsky, 2010 ). Interendothelial junctions of ECs, including tight junctions (TJs) and adherens junctions (AJs), are critical components of the physiological barrier. Occludin and vascular endothelial (VE)‍-cadherin are major representative TJ and AJ components ( Giannotta et al., 2013 Giannotta et al., 2013 ). LPS reduces the expression levels of occludin and VE-cadherin in PMVECs. Hydrogen-rich medium significantly increases the down-regulation and redistribution of occludin and VE-cadherin induced by LPS in PMVECs and Caco-2 cells ( Yang et al., 2016 Yang et al., 2016 ; Li Y et al., 2020 Li Y et al., 2020 ). In addition, LPS facilitates the formation of contractile stress fibers in the EC cytoskeleton ( Marcos-Ramiro et al., 2014 Marcos-Ramiro et al., 2014 ). This is mediated by RhoA activation of Rho kinase (ROCK) and myosin light chain kinase, accompanied by inhibition of myosin light chain phosphatase ( Schnittler, 2016 Schnittler, 2016 ). Hydrogen significantly ameliorates the excessive expression of ROCK, inhibits the activity of RhoA, prevents LPS-induced junctional injury and cell death, improves LPS-induced hyperpermeability of the endothelial barrier, and reduces the disruption of TJ and AJ ( Yang et al., 2016 Yang et al., 2016 ; Li Y et al., 2020 Li Y et al., 2020 ). HRS inhibits autophagy and has anti-apoptotic effects, alleviating LPS-induced ALI ( Wang et al., 2019 Wang et al., 2019 ). In mice, its effects are mediated by the ROS/adenosine 5'-monophosphate (AMP)‍-activated protein kinase (AMPK)/mTOR pathway. However, hydrogen can also inhibit the mTOR/TFEB signaling pathway, thereby increasing autophagy and alleviating LPS-induced endothelial dysfunction and apoptosis in ALI ( Fu et al., 2020 Fu et al., 2020 ). Despite these conflicting effects of hydrogen on autophagy, it clearly has a cytoprotective role in LPS-induced lung injury by modulating autophagy and apoptosis. 3.1.2　Protective function of hydrogen in ALI due to sepsis 3 Sepsis is a major cause of morbidity and mortality worldwide. It causes life-threatening organ dysfunction due to a dysfunctional host response to infection ( Singer et al., 2016 Singer et al., 2016 ). The lungs are highly vulnerable during sepsis ( Park et al., 2019 Park et al., 2019 ). Emerging evidence suggests that hydrogen can prevent sepsis, providing a novel treatment strategy for sepsis-induced ALI. The precise protective effects of hydrogen are summarized as follows. Hydrogen attenuates tissue injury and dysfunction by inhibiting HMGB-1. HMGB-1 often contributes to inflammatory disorders ( Andersson et al., 2018 Andersson et al., 2018 ). Hydrogen activates the Nrf2/HO-1 pathway, reduces HMGB-1 release in lung tissues of mice with sepsis, inhibits pro-inflammatory cytokines, increases the expression of antioxidant enzymes and anti-inflammatory cytokines, and increases mouse survival rates ( Xie et al., 2010 Xie et al., 2010 ; Li et al., 2015 Li et al., 2015 ; Yu et al., 2019 Yu et al., 2019 ). The protective effects of hydrogen are enhanced by its combination with other treatments. In zymosan-induced sepsis, the combination of inhalation of 2% hydrogen and hyperoxia had obvious beneficial effects on organs, including the lungs, liver, and kidneys ( Hong et al., 2016 Hong et al., 2016 ). Similarly, hydrogen inhalation combined with early fluid resuscitation significantly reduced increases in malonaldehyde (MDA) and MPO levels due to septic shock, and significantly increased SOD activity in lung tissue, thereby decreasing the degree of inflammation ( Liu et al., 2013 Liu et al., 2013 ). The combination of hydrogen with propofol improves the survival rate of mice with sepsis and reduces tissue damage and the release of cytokines ( Hong et al., 2017 Hong et al., 2017 ). In addition, the anti-oxidative effect of hydrogen can offset the side effects of other therapies. For example, hyperoxia may be beneficial in sepsis, but is accompanied by an increase in free radical formation and the exacerbation of organ injury in cecal ligation and puncture-induced ALI. Combination treatment with hydrogen and hyperoxia increases the therapeutic efficacy over that of monotherapy via both antioxidant and anti-inflammatory mechanisms, and markedly reduces the degree of ALI ( Xie et al., 2010 Xie et al., 2010 ). Mitochondrial dysfunction is involved in the progression of septic lung injury. Hydrogen blocks the opening of mitochondrial permeability transition pores and restores mitochondrial structure and function in sepsis-induced ALI ( Chen X et al., 2018 Chen X et al., 2018 ). Hydrogen can also activate autophagy, decreasing NLRP3 inflammasome activity, mitochondrial dysfunction, and cytokine release ( Chen HG et al., 2019 Chen HG et al., 2019 ). In addition, hydrogen improves mitochondrial quality control by enhancing mitophagy via the activation of the FUN14 domain-containing protein 1 (FUNDC1) pathway, thereby alleviating organ injury ( Yan et al., 2019 Yan et al., 2019 ). These results suggest that hydrogen targets mitochondria to improve energy metabolism in sepsis, alleviating mitochondrial dysfunction in the lungs. To fully understand the molecular mechanisms underlying the protective effect of hydrogen against sepsis, an isobaric tags for relative and absolute quantitation (iTRAQ)‍-based proteomic analysis of the murine lung with polymicrobial sepsis has been performed ( Bian et al., 2018 Bian et al., 2018 ). This study showed that 192 of 4472 differentially expressed proteins were related to the protective effects of hydrogen against sepsis. These proteins are associated with muscle contraction, oxygen transport, protein synthesis, collagen barrier membranes, cell adhesion, and coagulation function. Hydrogen also exerted protective effects via the downregulation of the expression of proteins which are involved in the regulation of immune function, cell death, and inflammation, and the upregulation of the expression of transferrin, which is an iron-binding protein with cytoprotective activity ( Bian et al., 2018 Bian et al., 2018 ). These results may facilitate the clinical application of hydrogen in patients with sepsis. 3.1.3　Role of hydrogen in viral pneumonia injury 3 Viral pneumonia has received substantial attention recently owing to the novel coronavirus. COVID-19 control remains a challenging task, and the treatments and prognoses of COVID-19 are different from influenza ( Bai and Tao, 2021 Bai and Tao, 2021 ). To date, specific antiviral drugs for the treatment of COVID-19 are lacking. Concentrations of inflammatory factors, such as IL-2, IL-7, IL-10, and TNF-‍α, in the plasma are higher in patients with severe or critical disease than in other patients ( Huang et al., 2005 Huang et al., 2005 ; Chien et al., 2006 Chien et al., 2006 ; Tang et al., 2020 Tang et al., 2020 ; Xu et al., 2020 Xu et al., 2020 ). Owing to its established antioxidant, anti-inflammatory, and anti-apoptotic effects, it is reasonable to use hydrogen in the early stage of COVID-19 to reduce the destructive cytokine storm and lung injury ( Yang FX et al., 2020 Yang FX et al., 2020 ). In rats treated with hydrogen-rich water (HRW), airway damage was alleviated, and mucin 5AC (MUC5AC) expression and mucus secretion in smoke-induced COPD models were decreased ( Ning et al., 2013 Ning et al., 2013 ). Hydrogen might be an effective agent for decreasing COVID-19-related viscous secretions. Although the direct use of hydrogen for the treatment of COVID-19 is a promising approach, additional experimental data are needed. In China, in the seventh edition of Chinese Clinical Guidance for COVID-19 Pneumonia Diagnosis and Treatment issued by the China National Health Commission (2020) China National Health Commission (2020) , the inhalation of oxygen mixed with hydrogen gas (33.3% O 2 and 66.6% H 2 ) is recommended. 3.1.4　Role of hydrogen in I/R injury of the lungs 3 I/R injury is associated with serious clinical manifestations, posing a serious therapeutic challenge for physicians ( Wu MY et al., 2018 Wu MY et al., 2018 ). The total tissue injury induced by I/R is divided into ischemia injury and reperfusion injury ( Gottlieb, 2011 Gottlieb, 2011 ). The pathophysiology of I/R injury involves ROS, aseptic inflammation, and cell death pathways. I/R injury in the lungs often develops during lung transplantation. Severe I/R injury leads to primary graft dysfunction. This is the major cause of short- and long-term morbidity and mortality after lung transplantation (den Hengst et al., 2010; Porteous et al., 2015 Porteous et al., 2015 ). Currently, there is no effective method for the prevention of I/R injury, and treatment strategies are focused on supportive care. Molecular hydrogen can reduce inflammation, oxidative stress, and apoptosis, and alleviate I/R injury. Inflammation induced by lung ischemia causes the release of the proinflammatory cytokines IL-8 and TNF-α and the activation of neutrophils during perfusion, resulting in EC damage, ultimately leading to alterations in permeability and lung edema. Hydrogen treatment decreased levels of IL-8, IL-1β, and TNF-‍α in the recipient lungs and serum, and decreased MPO levels in lung grafts ( Liu RF et al., 2015 Liu RF et al., 2015 ; Saito et al., 2020 Saito et al., 2020 ). Hydrogen also attenuated inflammatory response pathways, particularly the p38 MAPK and NF-‍κB pathways ( Zhang GC et al., 2018 Zhang GC et al., 2018 ). ·OH is the most detrimental ROS in I/R injury. Hydrogen can selectively scavenge ·OH and ONOO - ( Ohsawa et al., 2007 Ohsawa et al., 2007 ). Moreover, hydrogen inhalation during mechanical ventilation activates HO-1 (Kawamura et al., 2011), reduces MDA level, and increases SOD activity in rabbit lungs ( Kawamura et al., 2010 Kawamura et al., 2010 ; Li et al., 2012 Li et al., 2012 ). Apoptosis is also elevated after lung transplantation. Hydrogen significantly inhibits the proapoptotic proteins caspase-3 and caspase-8 in lung grafts and activates the Bcl-2 and B-cell lymphoma-xL (Bcl-xL), which inhibit apoptosis by stabilizing the mitochondrial outer membrane, and stop the release of cytochrome C into the cytosol via the intrinsic apoptotic pathway ( Kawamura et al., 2010 Kawamura et al., 2010 ; Liu RF et al., 2015 Liu RF et al., 2015 ). Hydrogen not only has protective effects in lung damage caused by lung transplantation itself, but also plays a role in I/R injury due to other causes. For example, in lung injury induced by intestinal or limb I/R due to clamping the bilateral femoral arteries for 3 h, compared to the control group, HRS treatment significantly decreased neutrophil infiltration, NF-‍κB activation, and levels of IL-‍1β, TNF-‍α, MPO, and MDA in the lung tissues, and downregulated chemerin and NLRP3, thereby attenuating apoptosis ( Mao et al., 2009 Mao et al., 2009 ; Zou et al., 2019 Zou et al., 2019 ). These findings suggest that hydrogen is a potential novel therapy to resolve the difficult clinical issue of lung I/R injury and may improve outcomes after lung transplantation and lung I/R resulting from other causes. 3.1.5　Effect of hydrogen on other types of lung injury 3 In hyperoxic ALI, by activating the PI3K/Akt/forkhead box O3a (FoxO3a) signaling pathway, hydrogen upregulates Sirt1, protects type II alveolar epithelial cells against hyperoxia-induced apoptosis, and alleviates ER stress ( Sun et al., 2017 Sun et al., 2017 ; Wu D et al., 2018 Wu D et al., 2018 ). In ventilator-induced lung injury (VILI), hydrogen gas inhalation effectively reduces VILI-associated inflammatory responses, including both local and systemic inflammation. Interestingly, hydrogen modulates the NF-‍κB signaling pathway by increasing NF-‍κB activation at an early stage of ventilation then decreasing it after 2 h of ventilation. The early activation of NF-κB was correlated with elevated levels of the antiapoptotic protein Bcl-2 and decreased levels of Bax. This may contribute to the cytoprotective effects of hydrogen against apoptotic and inflammatory signaling pathway activation, improve gas exchange, and reduce VILI-induced apoptosis ( Huang et al., 2010 Huang et al., 2010 , 2011 2011 ). These findings may provide guidance for single-lung ventilation anesthesia in thoracic surgery. In seawater instillation-induced ALI, 2% hydrogen gas inhalation attenuates lung injury by the activation of Nrf2 and HO-1 expression and inhibition of caspase-3 expression ( Diao et al., 2016 Diao et al., 2016 ). In addition, in ALI caused by oleic acid and burns (early stages of severe burn and extensive burn), hydrogen gas inhalation has a similar protective role ( Fang et al., 2011 Fang et al., 2011 ; Qin et al., 2017 Qin et al., 2017 ; Ying et al., 2017 Ying et al., 2017 ). These findings show that hydrogen has a broad range of potential applications for the treatment of diseases associated with lung injury. 3.2 Effects of hydrogen on COPD 2 COPD includes chronic bronchitis and pulmonary emphysema. It often leads to breathlessness and a reduction in exercise tolerance, thereby decreasing quality of life and increasing mortality ( Liu et al., 2011 Liu et al., 2011 ). Oxidative stress and inflammation play important roles in the pathogenesis of COPD ( Pinamonti et al., 1996 Pinamonti et al., 1996 ; Ricciardolo et al., 2006 Ricciardolo et al., 2006 ). By reducing CS exposure-induced COPD and inhibiting ERK1/2 and NF-‍κB in the lungs ( Liu et al., 2017 Liu et al., 2017 ; Lu et al., 2018 Lu et al., 2018 ), hydrogen can reduce CS-induced lung function decline, emphysema, inflammation, small-airway remodeling, and goblet-cell hyperplasia in the tracheal epithelium. It significantly reduces inflammatory cells in the bronchoalveolar lavage fluid, improves cardiovascular function, and reduces the right ventricular (RV) hypertrophy index. In addition to CS, other environmental risk factors, such as exposure to ambient inhaled toxicants ( DeVries et al., 2016 DeVries et al., 2016 ; Busch et al., 2017 Busch et al., 2017 ), can exacerbate COPD. The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor involved in mediating responses to human-made environmental toxicants ( Guerrina et al., 2018 Guerrina et al., 2018 ; Feng et al., 2019 Feng et al., 2019 ). A decline in AhR contributes to the pro-oxidative and pro-inflammatory effects of fine ambient particulate matter (PM 2.5 ) ( Yue et al., 2017 Yue et al., 2017 ). Hydrogen can effectively inhibit the AhR decline induced by concentrated ambient particles, and alleviate lung injury induced by exposure to concentrated ambient PM 2.5 , which is involved in the pathogenesis of COPD ( Feng et al., 2019 Feng et al., 2019 ). A clinical trial showed that 2.4% hydrogen gas inhaled for 45 min in patients with asthma or COPD decreases the levels of pro-inflammatory factors in the peripheral blood of patients and in exhaled breath condensates ( Wang ST et al., 2020 Wang ST et al., 2020 ). Hydrogen can reach lung cells easily and quickly, and act directly on the lungs, leading to good therapeutic efficacy ( Liu et al., 2011 Liu et al., 2011 ). Hydrogen is a novel candidate preventive and therapeutic strategy for COPD ( Liu et al., 2011 Liu et al., 2011 ). 3.3 Effects of hydrogen on asthma 2 Asthma is a chronic complex lung disease associated with airway inflammation, and leads to hyperreactivity, airflow limitation, and airway remodeling ( Haahtela, 1997 Haahtela, 1997 ; Comhair et al., 2000 Comhair et al., 2000 ). Endogenous and exogenous ROS play a major role in airway inflammation and are determinants of asthma severity ( Comhair et al., 2000 Comhair et al., 2000 , 2001 2001 ). Hydrogen can attenuate inflammation and oxidative stress in asthma. In ovalbumin-induced allergic airway inflammation, hydrogen gas inhalation reduces eosinophils and lymphocytes in bronchial alveolar lavage fluid (BALF), markedly decreases pro-inflammatory factors in the serum, upregulates the activity of SOD, and attenuates the increases in MDA and MPO ( Zhang N et al., 2018 Zhang N et al., 2018 ). Hydrogen significantly alleviates airway hyperresponsiveness and goblet cell hyperplasia, diminishes the T helper type 2 (T H 2) response, and decreases IL-4 as well as immunoglobulin E (IgE) levels by inhibiting NF-‍κB activation and activating the Nrf2 pathway ( Huang et al., 2019 Huang et al., 2019 ). Normally, alveolar macrophages in the lung function to maintain an airway clear of bacteria, foreign particles, and apoptotic cells. However, in asthma, the phagocytic ability of alveolar macrophages is significantly reduced. This defective phagocytosis is reversed by hydrogen gas inhalation ( Huang et al., 2019 Huang et al., 2019 ). In addition, hydrogen reduces airway remodeling which causes persistent alterations in airway wall structures and function, ultimately resulting in the progressive loss of lung function ( Fehrenbach et al., 2017 Fehrenbach et al., 2017 ). In ovalbumin-induced asthma, HRS inhibits the NF-‍κB pathway and significantly decreases the mucus index, the expression of MUC5AC, collagen III, and vascular endothelium growth factor (VEGF), and collagen deposition ( Xiao et al., 2013 Xiao et al., 2013 ), effectively alleviating airway remodeling. These results suggest that hydrogen alleviates allergic airway inflammation and improves airway function in asthma. Although research has been limited mainly to animal models, which imperfectly recapitulate asthma, these studies have improved our understanding of the benefits of hydrogen as a therapeutic intervention in asthma. Further studies are necessary to establish the clinical value of hydrogen. 3.4 Effects of hydrogen on lung cancer 2 Lung cancer is one of the most common lethal malignancies, with a poor prognosis owing to its high metastatic potential and drug resistance. An increasing number of animal experiments and clinical trials have established the efficacy of hydrogen against cancers, including lung cancer. The mechanisms underlying the anti-cancer effects of hydrogen are summarized as follows. Hydrogen downregulates the expression of proteins involved in stemness, proliferation, and angiogenesis and upregulates the expression of proteins that promote differentiation ( Liu et al., 2019 Liu et al., 2019 ). Hydrogen can also downregulate the chromosome condensation regulator structural maintenance of chromosomes 3 (SMC3), as well as the migration and invasion of A549 and H1975 cells, thereby inhibiting lung cancer progression ( Wang et al., 2018 Wang et al., 2018 ). Hydrogen modulates cell death. The dysregulation of apoptosis is a hallmark of cancer. The alteration of apoptosis contributes not only to tumor development and progression, but also to tumor resistance to therapies ( Pistritto et al., 2016 Pistritto et al., 2016 ). Hydrogen promotes apoptosis, including early and late apoptosis, in lung cancer ( Jiang et al., 2018 Jiang et al., 2018 ; Wang et al., 2018 Wang et al., 2018 ). The PI3K/Akt pathway is an important signaling pathway involved in extracellular signaling events and cellular processes, including cell proliferation, apoptosis, and survival. In non-small cell lung cancer, when combined with the PI3K inhibitor LY294002, hydrogen reduced cell proliferation and promoted apoptosis by downregulating Akt phosphorylation and inhibiting the PI3K pathway. Recently, it has been shown that hydrogen pretreatment enhances ROS and the expression of pyroptosis-related proteins, stimulates NLRP3 inflammasome/gasdermin D (GSDMD) activation, and inhibits endometrial cancer ( Yang Y et al., 2020 Yang Y et al., 2020 ). Further studies are needed to determine whether hydrogen can induce pyroptosis in lung cancer and to clarify the underlying molecular mechanism. Hydrogen modulates immunity by reducing the proportion of terminal programmed cell death 1 positive (PD-1 +‍ ) cluster of differentiation 8 positive (CD8 + ) T cells, which are associated with a poor prognosis in cancer ( Akagi, 2018 Akagi, 2018 ). In patients with lung cancer, hydrogen can activate coenzyme Q10, restore exhausted CD8 + T cells (especially PD-1 + Tim3 + terminal CD8 + T cells; Tim3 +‍ , T cell immunoglobulin and mucin domaincontaining protein 3 positive), enhance the clinical efficacy of nivolumab, and increase overall survival time ( Akagi and Baba, 2020 Akagi and Baba, 2020 ). Hydrogen can alleviate the side effects of conventional anti-cancer therapies, such as chemotherapy and radiotherapy, and improve quality of life. By reducing oxidative stress and inflammation, hydrogen protects cultured cells and mice against radiation-induced injury ( Qian et al., 2010 Qian et al., 2010 ; Qiu et al., 2020 Qiu et al., 2020 ). It also attenuates the gefitinib-induced exacerbation of naphthalene-induced ALI without impairing anti-tumor activity ( Terasaki et al., 2019b Terasaki et al., 2019b ). Hydrogen is well-suited for the treatment of advanced cancer. It significantly improves the physical status of patients, reduces fatigue, insomnia, anorexia, and pain, and decreases elevated tumor markers. These effects are particularly evident in patients with lung cancer ( Chen JB et al., 2019 Chen JB et al., 2019 ). As a simple, low-cost treatment with few adverse reactions, hydrogen therapy in lung cancer is very promising. 3.5 Effects of hydrogen on PAH 2 Pulmonary hypertension (PH) is a progressive complication of chronic lung disease (resting mean pulmonary artery pressure ≥25 mmHg (1 mmHg=133.3 Pa) ( Simonneau et al., 2019 Simonneau et al., 2019 ). PAH is one of most common forms of PH. Although therapies have improved the prognosis of patients with PAH, morbidity and mortality rates are still high ( Barst et al., 2012 Barst et al., 2012 ; Benza et al., 2012 Benza et al., 2012 ). PAH is a progressive vasculopathy involving an imbalance of vasodilators and vasoconstrictors, ROS, and inflammation ( Perez-Vizcaino et al., 2010 Perez-Vizcaino et al., 2010 ; Price et al., 2012 Price et al., 2012 ). The oral administration and injection of hydrogen have similar preventive effects against the development of PH and RV hypertrophy in monocrotaline (MCT)-induced PAH in rats ( Paulin et al., 2011 Paulin et al., 2011 ; Wang Y et al., 2011 Wang Y et al., 2011 ; He et al., 2013 He et al., 2013 ). Via its antioxidant and anti-inflammatory effects, hydrogen treatment effectively alleviates smooth muscle cell proliferation, increases vascular density, and alleviates PH and RV hypertrophy. Hydrogen can reduce 3-nitrotyrosine, which is a specific metabolic product of ONOO - and may participate in PH formation, decrease levels of MDA and 8-OHdG, and decrease SOD activity in PH ( Wang Y et al., 2011 Wang Y et al., 2011 ). Hydrogen could reduce ICAM-1, which is associated with the infiltration of chronic inflammatory cells in local lung tissues ( He et al., 2013 He et al., 2013 ). NF-κB plays a critical role in the progression of PAH, causing fibroblast growth factor 2 (FGF2)‍-induced inflammation in a rat model of MCT‍-induced PAH. Selectively inhibiting NF-‍κB can prevent the increase in RV pressure, suppress proliferation, and induce apoptosis in pulmonary arterial smooth muscle cells ( Hosokawa et al., 2013 Hosokawa et al., 2013 ). Hydrogen treatment effectively reduces inflammation and apoptosis by decreasing NF-‍κB activity ( Wang C et al., 2011 Wang C et al., 2011 ; Xie et al., 2012 Xie et al., 2012 ). These findings highlight the ability of hydrogen to modulate NF-‍κB-mediated inflammation in the pathogenesis of PAH. 3.6 Effect of hydrogen on PF 2 PF is a lung disease caused by aberrant wound healing due to repeated alveolar injury in genetically susceptible individuals. It is one of the major causes of morbidity, and effective treatments are lacking ( Osborn-Heaford et al., 2015 Osborn-Heaford et al., 2015 ). The pathology includes chronic inflammation, excess extracellular matrix (ECM) deposition, and scarring of lung tissue. The epithelial-mesenchymal transition (EMT) in ALI can cause the activation of myofibroblasts, which play a central role in the pathogenesis of PF via the synthesis and deposition of ECM proteins ( Cottin, 2013 Cottin, 2013 ; Zhang YQ et al., 2015 Zhang YQ et al., 2015 ). In addition, ROS and inflammation in ALI can induce a fibrotic response to lung injury by modulating ECM deposition ( Murthy et al., 2009 Murthy et al., 2009 ; He et al., 2011 He et al., 2011 ). HRS effectively suppresses oxidative stress, inhibits the LPS-induced activation of p38 MAPK and JNK, significantly decreases the LPS-induced loss of E-cadherin (an epithelial marker), and decreases α‍-smooth muscle actin (a myofibroblast marker) in lung tissues, thereby blocking alveolar EMT and PF. Additionally, hydrogen inhibits pulmonary transforming growth factor-‍‍β (TGF-‍‍β) production, which also takes part in the reprogramming of gene expression during EMT ( Tao et al., 2016 Tao et al., 2016 ). Hydrogen also alleviates PF caused by other factors, such as paraquat-induced lung fibroblast injury and rheumatoid arthritis‍‐‍associated interstitial lung disease ( Terasaki et al., 2019a Terasaki et al., 2019a ; Li T et al., 2020 Li T et al., 2020 ). Laboratory experiments have not verified the effects of hydrogen on idiopathic PF, which accounts for 25%–30% of cases of interstitial lung disease. There is convincing evidence that the EMT has important roles in organ fibrosis. TGF-‍β is a major EMT inducer, with a profibrotic effect in the lung epithelium during the pathological process of idiopathic PF ( Thiery et al., 2009 Thiery et al., 2009 ; Hewlett et al., 2018 Hewlett et al., 2018 ). We speculate that hydrogen can interfere with the process of idiopathic PF via related pathways, particularly given the great deal of overlap between mechanisms underlying idiopathic PF and other types of PF. However, further analyses are needed to evaluate this hypothesis. 4 Route of hydrogen administration 1 Hydrogen gas has some special characteristics, such as its nonpolarity, small size, and low solubility (1.6 ppm (part per million, ×10 -6 )) under physiological conditions. Typical administration routes include the inhalation of hydrogen gas, oral intake of HRW, and injection of HRS. Inhalation is a simple method in which a ventilator circuit, facemask, or nasal cannula is used to administer hydrogen gas. The effects are rapid, and it can be used to treat acute oxidative stress ( Ohta, 2014 Ohta, 2014 ). The oral intake of HRS, which is hydrogen dissolved in water, is a portable, safe, and convenient method for administration ( Sun et al., 2012 Sun et al., 2012 ; Koyama et al., 2014 Koyama et al., 2014 ). Under normal atmospheric pressure and at room temperature, hydrogen can be dissolved in water up to 0.8 mmol/L (1.6 mg/L) ( Asada et al., 2020 Asada et al., 2020 ). The injection of HRS can provide highly accurate hydrogen doses. Either peritoneal or intravenous injection can be applied to provide a protective effect ( Yan et al., 2017 Yan et al., 2017 ; Ying et al., 2017 Ying et al., 2017 ; Xu et al., 2018 Xu et al., 2018 ). In addition, intrathecal injection can produce neuro-protective effects ( Ge et al., 2014 Ge et al., 2014 ). Its lack of polarity and easy cell penetration make hydrogen promising for the treatment of skin and eye diseases with topical formulations and eye drops ( Asada et al., 2019 Asada et al., 2019 ; Cejka et al., 2020 Cejka et al., 2020 ). However, these applications of hydrogen often do not achieve highly targeted effects. Targeted delivery and controlled release of hydrogen can address this issue ( Kawamura M et al., 2020 Kawamura M et al., 2020 ). Recently, investigators have designed palladium (Pd) hydride nanocrystals as a multifunctional hydrogen carrier for tumor-targeted delivery and the controlled release of bio-reductive hydrogen. This method not only has anticancer effects, but also protects normal cells from hyperthermia damage ( Zhao et al., 2018 Zhao et al., 2018 ). A similar nanomedicine strategy has been used to alleviate oxidative stress and I/R injury ( Kou et al., 2019 Kou et al., 2019 ; Kawamura T et al., 2020 Kawamura T et al., 2020 ). These applications of molecular hydrogen provide new avenues for the treatment of lung diseases, especially for lung cancer. The routes of hydrogen administration are summarized in Table 1 Table 1 . Dosage form Administration route Characteristics Hydrogen gas Inhalation Simple method; rapid action 2 Hydrogen water Oral intake 2 Portable, safe, and convenient Bath 4 Hydrogen saline Peritoneal injection 4 Provides highly accurate hydrogen doses; produces neuro-protective effects; treats eye diseases Intravenous injection Intrathecal injection Eye drops 2 Hydrogen nanocrystals Oral intake 2 Highly targeted effects Injection There are many routes for hydrogen administration, such as hydrogen gas inhalation, oral intake or a hydrogen water bath, injection of hydrogen saline (including peritoneal, intravenous and intratheral injection), and local eye drops. To achieve highly targeted effects, hydrogen can also be designed as nanocrystals, providing a new avenue for the treatment of lung diseases such as lung cancer. 5 Conclusions and perspectives 1 There is accumulating evidence for the broad biological effects of hydrogen. It regulates oxidative stress, inflammation, autophagy, programmed cell death, and the aging process. Animal experiments and clinical trials have clearly demonstrated the protective effects of hydrogen on many organs and systems. In particular, there is increasing evidence that hydrogen exerts a protective effect in various lung diseases. From a systemic perspective, in addition to the direct protective effects of hydrogen on the lungs, it indirectly protects lung tissues via protective effects on other tissues and organs. However, the detailed molecular mechanisms underlying the protective effects of hydrogen remain to be determined, and our current understanding of its effects is based mainly on animal experiments. Applicability to humans is yet to be tested. Therefore, a better understanding of protective pathways mediating the effects of hydrogen may facilitate the design of specific therapies for the treatment of pulmonary diseases. 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Shock , 52 ( 1 ): 134 - 141 . https://doi.org/10.1097/SHK.0000000000001194 https://doi.org/10.1097/SHK.0000000000001194 Hydrogen-rich saline attenuates acute lung injury induced by limb ischemia/reperfusion via down-regulating chemerin and NLRP3 in rats Zhiling FU analyzed the literature and prepared the first draft of the manuscript. Jin ZHANG revised, edited, and checked the final version. Both authors have read and approved the final manuscript, and therefore, have full access to all the data in the study and take responsibility for the integrity and security of the data. This study was supported by the Technology Bureau of Liaoning Province (No. 17-230-9-45), China. 10.1631/jzus.B2100420 1673-1581（2022）02-0102-21 This study was supported by the Technology Bureau of Liaoning Province (No. 17-230-9-45), China. 2021-05-10 2021-09-07 2022-02-15 2022-04-19 2022-01-04 Copyright © Zhejiang University and Springer-Verlag GmbH Germany, part of Springer Nature 2022 2022 浙江大学出版社 Zhiling FU and Jin ZHANG declare that they have no conflict of interest. This article does not contain any studies with human or animal subjects performed by either of the authors. Compliance with ethics guidelines 浙江大学学报（英文版）（B辑：生物医学和生物技术） 2 23