Bajaj Payal, Kaur Tajpreet, Singh Amrit Pal, Kaur Gurcharan
Medical Biotechnology Laboratory, Department of Biotechnology, Guru Nanak Dev University, Amritsar, 143005, Punjab, India.
Department of Pharmacology, Khalsa College of Pharmacy, Amritsar, 143005, India.
Lab Anim Res. 2024 Aug 21;40(1):29. doi: 10.1186/s42826-024-00216-4.
Sleep deprivation (SD) due to an unhealthy lifestyle poses an oxidative challenge and is closely associated with an increased risk and prevalence of different metabolic disorders. Although the negative consequences of SD are well reported on mental health little is known about its detrimental effects on liver function and lipid metabolism. Tinospora cordifolia is reported for its hepatoprotective activity in different pre-clinical model systems. The current study was designed to elucidate the cumulative effects of aging and acute SD on liver functions, oxidative stress, and lipid metabolism, and their management by butanol extract of T. cordifolia (B-TCE) using middle-aged female acyclic rats as the model system.
Rats were divided into 4 groups: (1) Vehicle-undisturbed (VUD) (2) Vehicle-sleep deprived (VSD) (3) B-TCE pre-treated sleep-deprived (TSD) (4) B-TCE pre-treated undisturbed sleep (TUD). TSD and TUD groups were given 35 mg/kg of B-TCE once daily for 15 days followed by 12 h of sleep deprivation (6 a.m.-6 p.m.) of VSD and TSD group animals using the gentle-handling method while VUD and TUD group animals were left undisturbed. SD of VSD group animals increased oxidative stress, liver function disruption, and dyslipidemia which were ameliorated by B-TCE pre-treatment. Further, B-TCE was observed to target AMPK and its downstream lipid metabolism pathways as well as the p-Akt/cyclinD1/p-bad pathway of cell survival as possible underlying mechanisms of its hepatoprotective activity.
These findings suggest that B-TCE being a multi-component extract may be a potential agent in curtailing sleep-related problems and preventing SD-associated hepatotoxicity and dyslipidemia in postmenopausal women.
不健康的生活方式导致的睡眠剥夺(SD)会带来氧化应激挑战,并且与不同代谢紊乱风险及患病率增加密切相关。尽管睡眠剥夺对心理健康的负面影响已有充分报道,但对其对肝功能和脂质代谢的有害影响却知之甚少。在不同的临床前模型系统中,已报道了心叶青牛胆具有肝脏保护活性。本研究旨在以中年雌性非周期性大鼠为模型系统,阐明衰老和急性睡眠剥夺对肝功能、氧化应激和脂质代谢的累积影响,以及心叶青牛胆丁醇提取物(B-TCE)对它们的调控作用。
将大鼠分为4组:(1)载体未受干扰组(VUD)(2)载体睡眠剥夺组(VSD)(3)B-TCE预处理睡眠剥夺组(TSD)(4)B-TCE预处理未受干扰睡眠组(TUD)。TSD组和TUD组每天给予35mg/kg的B-TCE,持续15天,随后采用轻柔处理方法对VSD组和TSD组动物进行12小时的睡眠剥夺(上午6点至下午6点),而VUD组和TUD组动物则不做处理。VSD组动物的睡眠剥夺增加了氧化应激、肝功能破坏和血脂异常,而B-TCE预处理可改善这些情况。此外,观察到B-TCE靶向AMPK及其下游脂质代谢途径以及细胞存活的p-Akt/cyclinD1/p-bad途径,这可能是其肝脏保护活性的潜在机制。
这些发现表明,作为一种多成分提取物,B-TCE可能是减少与睡眠相关问题以及预防绝经后女性睡眠剥夺相关肝毒性和血脂异常的潜在药物。