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珊瑚钙携带氢可改善胆碱缺乏型高碳水化合物无脂肪饮食诱导的老年大鼠非酒精性脂肪性肝炎的严重程度。

Coral calcium carried hydrogen ameliorates the severity of non-alcoholic steatohepatitis induced by a choline deficient high carbohydrate fat-free diet in elderly rats.

机构信息

Division of Transplantation Immunology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.

Acche Corporation, Tokyo, Japan.

出版信息

Sci Rep. 2023 Jul 19;13(1):11646. doi: 10.1038/s41598-023-38856-6.

DOI:10.1038/s41598-023-38856-6
PMID:37468618
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10356788/
Abstract

Hydrogen has been reported to act as an antioxidant, anti-apoptosis and anti-inflammatory agent. Coral calcium carried hydrogen (G2-SUISO) is a safer and more convenient form of hydrogen agent than others. The mechanism underlying the hepatoprotective effects of G2-SUISO using an elderly non-alcoholic steatohepatitis (NASH) rat model was investigated. Two days after fasting, six-month-old elderly male F344/NSlc rats were given a choline deficient high carbohydrate fat-free (CDHCFF) diet from day 0 to day 3 as CDHCFF control group, and then switched to a normal diet from days 4 to 7 with or without 300 mg/kg G2-SUISO. Rats in each group were finally being sacrificed on day 3 or day 7. In the CDHCFF diet group, G2-SUISO decreased the liver weight-to-body weight ratio, the serum AST, ALT, total cholesterol levels, inflammatory infiltration, pro-inflammatory cytokine expression and lipid droplets with inhibiting lipogenic pathways by reducing sterol regulatory element-binding protein-1c, acetyl-CoA carboxylase and fatty acid synthase gene expression compared with the CDHCFF diet alone. G2-SUISO had beneficial effects of anti-apoptosis as well the down-regulation of pro-apoptotic molecules including NF-κB, caspase-3, caspase-9 and Bax. These findings suggest that G2-SUISO treatment exerts a significant hepatoprotective effect against steatosis, inflammation and apoptosis in elderly NASH rats.

摘要

氢已被报道具有抗氧化、抗凋亡和抗炎作用。携带氢的珊瑚钙(G2-SUISO)是一种比其他形式更安全、更方便的氢供体。本研究旨在探讨 G2-SUISO 对老年非酒精性脂肪性肝炎(NASH)大鼠模型的保肝作用机制。禁食 2 天后,6 月龄老年雄性 F344/NSlc 大鼠从第 0 天至第 3 天给予胆碱缺乏高碳水化合物无脂肪(CDHCFF)饮食作为 CDHCFF 对照组,然后从第 4 天至第 7 天转换为正常饮食,或同时给予 300mg/kg G2-SUISO。每组大鼠最终于第 3 天或第 7 天处死。在 CDHCFF 饮食组中,与单独给予 CDHCFF 饮食相比,G2-SUISO 降低了肝重/体重比、血清 AST、ALT、总胆固醇水平、炎症浸润、促炎细胞因子表达和脂滴,通过降低固醇调节元件结合蛋白-1c、乙酰辅酶 A 羧化酶和脂肪酸合酶基因表达抑制了生脂途径。G2-SUISO 还具有抗凋亡作用,下调了包括 NF-κB、caspase-3、caspase-9 和 Bax 在内的促凋亡分子。这些发现表明,G2-SUISO 治疗对老年 NASH 大鼠的脂肪变性、炎症和凋亡具有显著的保肝作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/742e/10356788/2db18f05f560/41598_2023_38856_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/742e/10356788/0db50efcc5eb/41598_2023_38856_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/742e/10356788/2fbae91a94b4/41598_2023_38856_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/742e/10356788/21ec9a6da56c/41598_2023_38856_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/742e/10356788/5e66847baa17/41598_2023_38856_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/742e/10356788/2db18f05f560/41598_2023_38856_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/742e/10356788/0db50efcc5eb/41598_2023_38856_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/742e/10356788/2fbae91a94b4/41598_2023_38856_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/742e/10356788/21ec9a6da56c/41598_2023_38856_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/742e/10356788/5e66847baa17/41598_2023_38856_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/742e/10356788/2db18f05f560/41598_2023_38856_Fig5_HTML.jpg

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