Hypolipidemic activity of low-cholesterol ovum oil of Rana chensinensis and phytosterol (stigmasterol) in rats#

Hypolipidemic activity of low-cholesterol ovum oil of Rana chensinensis and phytosterol (stigmasterol) in rats # # 低胆固醇林蛙卵油和植物甾醇(豆甾醇)在大鼠中的降脂作用 first-author corresp ‡Corresponding Author ‡Corresponding Author †E-mail:zhangth@jlu.edu.cn †E-mail:zhangth@jlu.edu.cn zhangth@jlu.edu.cn College of Food Science and Engineering, Jilin University, Changchun 130062, China College of Food Science and Engineering, Jilin University, Changchun 130062, China The ovum oil of forest frog has various health beneficial functions. In the current research, we evaluated the hypolipidemic effects of the low-cholesterol ovum oil from the forest frog and its combination with stigmasterol in rats. 目的 2 探索林蛙副产物林蛙卵油的开发价值. 创新点 2 首次验证了低胆固醇林蛙卵油的减重降脂功能. 方法 2 Sprague-Dawley大鼠连续被灌胃8周后,分成8组:(1)对照组喂食标准饲料;(2)高脂组喂食60%高脂饲料;(3)阳性对照组喂食3.33 mg/(kg·d)辛伐他汀;(4)OORC组喂食2 g/(kg·d)的低胆固醇林蛙卵油(OORC);(5)植物甾醇组喂食 0.48 g/(kg·d)的豆甾醇;(6)低剂量组喂食1 g/(kg·d)的低胆固醇OORC和0.24 g/(kg·d)的豆甾醇;(7)中剂量组喂食2 g/(kg·d)的低胆固醇OORC和0.48 g/(kg·d)的豆甾醇;(8)高剂量组喂食4 g/(kg·d)的低胆固醇OORC 和0.96 g/(kg·d)的豆甾醇.经过不同方法处理后,比较各组大鼠的体重、器官指数,以及血清中总胆固醇、甘油三酯、低密度脂蛋白和高密度脂蛋白浓度.同时,对动物肝脏进行组织切片染色并评价损伤情况. 结论 2 低胆固醇林蛙卵油或者其与植物甾醇(如豆甾醇)联用可以预防高脂饮食诱导的增重、肝损伤和高血脂症状. Ovum oil of Rana chensinensis Forest frog Hyperlipidemia 林蛙卵油 林蛙 肥胖 高血脂 The ovum oil of forest frog has various health beneficial functions. In the current research, we evaluated the hypolipidemic effects of the low-cholesterol ovum oil from the forest frog and its combination with stigmasterol in rats. The forest frog, Rana chensinensis , has been consumed as a precious tonic food for years as it is known to nourish the body and has many pharmacological effects (Bao et al., 2016 2016 ). The ovum oil of R . chensinensis (OORC) is rich in unsaturated fatty acids (Jin et al., 2004 2004 ) that can alleviate hyperlipidemia. Since forest frog oil (Hasma) is sold at high prices, the other parts of the frog are treated as by-products and often used to feed animals (Wang et al., 2015 2015 ). OORC is an important part of the forest frog and is rich in proteins and unsaturated fatty acids that can improve the immune system and delay senescence (Ji et al., 2013 2013 ). However, high intake of cholesterol has long been linked with health problems (Yu et al., 2013 2013 ). In the current study, we used low-cholesterol OORC, which has reduced cholesterol levels but high unsaturated fatty acid levels (Zhang et al., 2019 2019 ). As reported previously, plant sterols, when sometimes consumed with other nutrients, also effectively reduce fat absorption in the intestine and decrease the levels of total blood lipids and low-density lipoproteins with no negative effects on the levels of high-density lipoproteins (Chen et al., 2005 2005 ). Therefore, we aimed to investigate the effects of low-cholesterol OORC and its combination with the phytosterol (stigmasterol) in improving lipid profiles, which may provide a theoretical basis for the development of functional foods that prevent hyperlipidemia. After five weeks of feeding, Sprague-Dawley rats that were fed a high-fat diet had significantly higher body weights than rats that were fed a standard diet ( P < 0.05). Unexpectedly, the positive control group, in which rats were administered simvastatin, was not significantly different from high-fat-induced hypolipidemic rats with respect to weight. However, the other groups of rats treated with OORC, phytosterol (stigmasterol), or their combinations, had significantly lower body weights than the high-fat-induced hypolipidemic rats ( P < 0.05). Details are shown in Data S1 S1 . Rats that were fed a high-fat diet, with or without any intervention, had moderately higher hepatic indexes, which indicated that the increased weights of the liver were probably caused by fat accumulation. However, only the group that was concurrently fed a low dose of OORC and phytosterol reached statistically significant levels (Table S1 S1 ). No significant difference was observed between the splenic indexes. Hyperlipidemia is characterized by abnormal blood lipid profiles. Compared to those in the normal group, the total cholesterol (TC), triglycerides (TG), and low-density lipoprotein cholesterol (LDL-C) levels in the sera of the hyperlipidemic group were found to be significantly increased ( P < 0.05), whereas the high-density lipoprotein cholesterol (HDL-C) level was found to be significantly decreased ( P < 0.05), indicating that the high-fat diet caused hyperlipidemia in rats (Fig. 1 1 ). Simvastatin, OORC, phytosterol, and the OORC-phytosterol combination improved their respective lipid profiles by reducing TG and LDL-C levels and increasing HDL-C levels ( P < 0.05). No significant difference was observed between the treatments of simvastatin, OORC, phytosterol, and the OORC-phytosterol combination with respect to blood lipid regulation. OORC and phytosterol also showed an effect similar to that of simvastatin with respect to hyperlipidemia prevention in rats. Lipid profiles that included TG (a), TC (b), HDL-C (c), and LDL-C (d) were observed to improve after simvastatin, OORC, and phytosterol (stigmasterol) treatments. No significant difference was observed between the treatments of simvastatin, OORC, phytosterol, and OORC-phytosterol combination. Values represent mean±standard deviation (SD), with n =8. * represents significant difference between the hyperlipidemic and normal groups with respect to the corresponding index ( P < 0.05); # represents significant difference when compared to the hyperlipidemia model group with respect to the corresponding index ( P < 0.05). TG, triglycerides; TC, total cholesterol; LDL-C, low-density lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol; NC, normal control group; HL, hyperlipidemic group; PC, positive simvastatin control group; P, phytosterol group; O, ovum oil of R . chensinensis (OORC) group; LOP, low dose of OORC-phytosterol group; MOP, middle dose of OORC-phytosterol group; HOP, high dose of OORC-phytosterol group Hyperlipidemia is caused by abnormal blood lipid metabolism that mainly manifests under high TC, TG, and LDL-C levels or low HDL-C levels in the blood (Bahmani et al., 2015 2015 ). HDL-C transports cholesterol from the extrahepatic tissue to the liver for degradation, which is then distributed to the whole body in order to reduce cholesterol deposition. On the other hand, LDL-C transports the cholesterol synthesized in the liver to the whole body. Hyperlipidemia is a risk factor for cardiovascular diseases (Nelson, 2013 2013 ). Accumulation of serum cholesterol in blood vessels can lead to heart disease, strokes, and cardiovascular diseases (Cholesterol Treatment Trialists’ (CTT) Collaboration, 2015 2015 ). Therefore, inhibition of cholesterol synthesis via drugs or diet therapy has been the primary strategy to reduce risk of cardiovascular diseases for years. The most important finding of the current research was that low-cost OORC demonstrated effective cholesterol-lowering effects and tremendous potential as a functional food or as an adjunct medicine to prevent and/or treat hyperlipidemia. In the normal group, liver cells were normally shaped and neatly arranged with no fat infiltration. In the hyperlipidemic group, many small vacuoles were observed in the liver cells. Furthermore, the OORC, phytosterol, and OORC-phytosterol groups showed improved liver phenotypes (since more normal hepatocytes were found in the liver) when compared to the hyperlipidemic group (Fig. 2 2 ). The representative H & E-stained liver slice images are listed as follows: NC (normal control group), HL (hyperlipidemic group), PC (positive simvastatin control group), P (phytosterol group), O (ovum oil of R . chensinensis (OORC) group), LOP (low dose of OORC-phytosterol group), MOP (middle dose of OORC-phytosterol group), and HOP (high dose of OORC-phytosterol group). Different from the healthy, many small vacuoles were observed in the liver cells of the hyperlipidemic rats. Administration of OORC, phytosterol, or OORC-phytosterol improved liver phenotypes. Arrow 1, inflammatory cell infiltration; Arrow 2, liver cytoplasm mesh shape (small cavity), nuclear enrichment. 200×magnification Due to several side effects of the currently used lipid-lowering drugs, natural medicine has attracted the attention of the scientific community. Phytosterols are known to improve blood lipid profiles. As reported previously, unsaturated fatty acids either alone or combined with phytosterols can help remove cholesterol esters generated within the body by regulating lipoproteins (Park and Carr, 2013 2013 ). Therefore, OORC can be used in combination with phytosterols to prevent hyperlipidemia, which is confirmed in our study. In conclusion, OORC, phytosterol (stigmasterol), and a combination of both showed lipid-lowering functions in our study. Interestingly, the OORC-phytosterol and OORC groups showed no significant difference in their results. Furthermore, no synergistic effect between phytosterol and OORC was observed. Therefore, OORC and phytosterol (stigmasterol) show similar effects with respect to improving the lipid profile. Overall, OORC is a healthy food component that can be consumed by people looking to prevent hyperlipidemia. References M Bahmani , M Mirhoseini , H Shirzad , 等 . A review on promising natural agents effective on hyperlipidemia . 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Optimization of conditions for cholesterol removal from Rana chensinensis ovum oil . Curr Topics Nutraceut Res , 2019 . 17 ( 2 ): 135 - 139 . . Optimization of conditions for cholesterol removal from Rana chensinensis ovum oil Compliance with ethics guidelines Chang-hui ZHAO, Chao ZHAO, Hai-qing YE, Chun-yu XI, Zheng-ping ZOU, Xin-hui ZHOU, Ping-ping HOU, and Tie-hua ZHANG declare that they have no conflicts of interest. All institutional and national guidelines for the care and use of laboratory animals were followed. 10.1631/jzus.B1900018 Project supported by the Jilin Province Research and Industrialization with Key Technologies for High Value Processing and Safety Control of Agricultural Products (No. SF2017-6-4) and the Jilin Provincial Department of Education (No. JJKH20180172KJ), China 2019-01-21 2019-03-24 2022-01-05 Copyright © Zhejiang University and Springer-Verlag GmbH Germany, part of Springer Nature 2019 2019 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 07 20