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叔丁基对苯二酚对断奶后高脂肪饮食喂养大鼠肥胖诱导的骨骼肌病变的保护作用。

Protective Effect of Tertiary Butylhydroquinone against Obesity-induced Skeletal Muscle Pathology in Post-weaning High Fat Diet Fed Rats.

机构信息

Department of Pediatrics, Hanzhong Central Hospital, Hanzhong, 723000, China.

出版信息

Curr Pharm Biotechnol. 2024;25(10):1276-1287. doi: 10.2174/1389201024666230810094809.

Abstract

BACKGROUND

Obesity deleteriously affects skeletal muscle functionality starting from infancy to adulthood, leading to dysfunctional skeletal muscle.

OBJECTIVES

This study, therefore, evaluated the protective action of tert-butylhydroquinone (tBHQ) against obesity-induced skeletal muscle pathology in high-fat diet (HFD) fed rats.

METHODS

Twenty post-weaning male albino rats were randomized into four groups of five rats each as: Group 1 (control), Group 2 (HFD), Group 3 (orlistat) and Group 4 (tBHQ). Group one received rat pellets for 12 weeks, while groups 2 to 4 received HFD for 12 weeks. At the end of week 8, obesity was confirmed with Lee Obesity Index and body mass index values of ≥ 303 and ≥ 0.68 gcm, respectively. Group 3 was given oral administration of orlistat (10 mg/kg, once daily), while group 4 was given oral administration of tBHQ (25 mg/kg, once daily). Administration of orlistat and tBHQ commenced from week 9 to the end of the experiment.

RESULTS

Chronic exposure of post-weaning rats to HFD led to their development of the metabolic syndrome phenotypes in adulthood, characterized by obesity, hyperglycemia, dyslipidaemia, hyperinsulinaemia, insulin resistance as well as induction of oxidative stress and alteration of skeletal muscle markers, which were mitigated following supplementation with orlistat and tBHQ.

CONCLUSION

The study showed the anti-obesity potentials of tBHQ and its protective action against HFD obesity-induced skeletal muscular pathology.

摘要

背景

肥胖从婴儿期到成年期都会对骨骼肌功能产生有害影响,导致骨骼肌功能障碍。

目的

因此,本研究评估了叔丁基对苯二酚(tBHQ)对高脂肪饮食(HFD)喂养大鼠肥胖诱导的骨骼肌病变的保护作用。

方法

将 20 只断奶后雄性白化大鼠随机分为四组,每组 5 只:第 1 组(对照组)、第 2 组(HFD 组)、第 3 组(奥利司他组)和第 4 组(tBHQ 组)。第 1 组接受大鼠颗粒饲料 12 周,而第 2 至 4 组接受 HFD 12 周。在第 8 周末,用 Lee 肥胖指数和身体质量指数值≥303 和≥0.68 gcm 分别确认肥胖。第 3 组给予奥利司他(10mg/kg,每日一次)口服给药,第 4 组给予 tBHQ(25mg/kg,每日一次)口服给药。奥利司他和 tBHQ 的给药从第 9 周开始持续到实验结束。

结果

幼年期慢性暴露于 HFD 会导致成年期代谢综合征表型的发展,其特征为肥胖、高血糖、血脂异常、高胰岛素血症、胰岛素抵抗以及氧化应激的诱导和骨骼肌标志物的改变,这些改变在补充奥利司他和 tBHQ 后得到缓解。

结论

本研究表明 tBHQ 具有抗肥胖潜力,可预防 HFD 肥胖引起的骨骼肌病变。

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