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去酰基胃饥饿素可刺激瘦鼠的类固醇生成,并逆转高脂饮食喂养大鼠的生殖功能障碍。

Unacylated ghrelin stimulates steroidogenesis in lean rats and reverses reproductive dysfunction in high fat diet-fed rats.

作者信息

Dallak Mohammad

机构信息

a Department of Physiology, College of Medicine , King Khalid University , Abha , Saudi Arabia.

出版信息

Syst Biol Reprod Med. 2019 Apr;65(2):129-146. doi: 10.1080/19396368.2018.1523971. Epub 2018 Sep 28.

Abstract

This study investigated the effect of sub-chronic administration of unacylated ghrelin (UAG) on steroidogenesis, sperm parameter, and reproductive function in lean and high fat diet (HFD)-induced obese male rats. Rats were divided into 4 groups (n = 12 each) as 1) Control-fed standard diets (STD): (10 kcal%), 2) STD + UAG (200 ng/kg, i.p.), 3) HFD obese: fed HFD (45 kcal%), and 4) HFD + UAG. Diet regimen was continued for 16 weeks after which normal saline as a vehicle or UAG was administered to desired groups for the next 4 weeks. In vitro, testicular slices were incubated with increasing concentrations of UAG (10-10 M) in the presence or absence of GSH-R1a antagonist, [D-Lys-3]-GHRP-6 (10 M). UAG significantly increased the circulatory levels of FSH, LH and testosterone, increased testicular testosterone levels and sperm count and motility in lean and obese rats and reduced sperm morphological abnormalities and increased pregnancy rate and number of pups at birth in HFD-obese rats. Associated with the reduction in the final body and fat masses weights and independent of food intake, UAG post-therapy to both lean and HFD-fed rats significantly lowered fasting blood glucose and insulin levels, lowered HOMA-IR value, enhanced OGTT and ITT, lowered circulatory leptin levels, downregulated aromatase expression in adipose and testicular tissue and inhibited HFD-induced testicular oxidative stress and activation of cleaved caspase-3. Dysregulation of testicular levels of StAR, SF-1, CYP11A1 in the testis of both groups as well as in the in vitro preparation, in a dose-dependent manner, independent of GSH-R1a and not associated with activation of STAT3, a mediator of leptin signaling was apparent. In conclusion, administration of UAG can enhance reproductive function in lean rats and reverses HFD-induced reproductive dysfunction in obese rats. Abbreviations: AG: acylated ghrelin; BMI: body mass index; CHOL: cholesterol;FSH: follicular stimulating hormone; GHS: growth hormone secretagogues; GSH: reduced glutathione; HFD: high fat diet; HOMA-IR: homeostasis model assessment of insulin resistance: IR: insulin resistance; OGTT: oral glucose tolerance test; ITT: insulin tolerance test; LH: luteinizing hormone; MDA: malondialdehyde; STAT3: signal transducer and activator of transcription; SOD: superoxide dismutase; STD: standard diet; SF-1: steroidogenic factor-1; StAR: steroidogenic acute regulatory protein; CYP11A1: cholesterol side-chain cleavage enzyme (or P450scc); TGs: triglycerides; UAG: unacylated ghrelin.

摘要

本研究调查了亚慢性给予去酰基胃饥饿素(UAG)对正常饮食及高脂饮食(HFD)诱导的肥胖雄性大鼠的类固醇生成、精子参数及生殖功能的影响。大鼠被分为4组(每组n = 12):1)标准饮食对照组(STD):(10千卡%);2)STD + UAG(200 ng/kg,腹腔注射);3)HFD肥胖组:给予HFD(45千卡%);4)HFD + UAG组。饮食方案持续16周,之后在接下来的4周内,对相应组给予生理盐水或UAG。体外实验中,在存在或不存在谷胱甘肽受体1a拮抗剂[D - Lys - 3]-GHRP - 6(10 μM)的情况下,将睾丸切片与浓度递增的UAG(10 - 10 M)一起孵育。UAG显著提高了正常饮食和肥胖大鼠体内促卵泡生成素(FSH)、促黄体生成素(LH)和睾酮的循环水平,增加了睾丸睾酮水平、精子数量及活力,减少了精子形态异常,并提高了HFD肥胖大鼠的妊娠率和出生幼崽数量。与最终体重和脂肪量的减少相关且与食物摄入量无关,对正常饮食和HFD喂养的大鼠进行UAG治疗后,显著降低了空腹血糖和胰岛素水平,降低了胰岛素抵抗的稳态模型评估(HOMA - IR)值,增强了口服葡萄糖耐量试验(OGTT)和胰岛素耐量试验(ITT),降低了循环中的瘦素水平,下调了脂肪和睾丸组织中芳香化酶的表达,并抑制了HFD诱导的睾丸氧化应激和裂解型半胱天冬酶 - 3的激活。两组大鼠睾丸中类固醇生成急性调节蛋白(StAR)、类固醇生成因子 - 1(SF - 1)、胆固醇侧链裂解酶(CYP11A1)水平以及体外实验制剂中的水平均出现剂量依赖性失调,与谷胱甘肽受体1a无关,且与瘦素信号传导介质信号转导和转录激活因子3(STAT3)的激活无关。总之,给予UAG可增强正常饮食大鼠的生殖功能,并逆转HFD诱导的肥胖大鼠生殖功能障碍。缩写:AG:酰基化胃饥饿素;BMI:体重指数;CHOL:胆固醇;FSH:促卵泡生成素;GHS:生长激素促分泌素;GSH:还原型谷胱甘肽;HFD:高脂饮食;HOMA - IR:胰岛素抵抗的稳态模型评估;IR:胰岛素抵抗;OGTT:口服葡萄糖耐量试验;ITT:胰岛素耐量试验;LH:促黄体生成素;MDA:丙二醛;STAT3:信号转导和转录激活因子;SOD:超氧化物歧化酶;STD:标准饮食;SF - 1:类固醇生成因子 - 1;StAR:类固醇生成急性调节蛋白;CYP11A1:胆固醇侧链裂解酶(或P450scc);TGs:甘油三酯;UAG:去酰基胃饥饿素

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