Department of Neuroscience & Experimental Therapeutics, Albany Medical College, 47 New Scotland Avenue, MC-136, Albany, NY, 12208, USA.
Department of Physiology, Tulane University School of Medicine, New Orleans, LA, 70112, USA.
Int J Obes (Lond). 2024 Dec;48(12):1839-1843. doi: 10.1038/s41366-024-01618-z. Epub 2024 Aug 17.
Menopause accelerates metabolic dysfunction, including (pre-)diabetes, obesity and visceral adiposity. However, the effects of endocrine vs. chronological aging in this progression are poorly understood. We hypothesized that menopause, especially in the context of middle-age, would exacerbate the metabolic effects of a high fat diet. Using young-adult and middle-aged C57BL/6J female mice, we modeled diet-induced obesity via chronic administration of high fat (HF) diet vs. control diet. We modeled peri-menopause/menopause via injections of 4-vinylcyclohexene diepoxide, which accelerates ovarian failure vs. vehicle. We performed glucose tolerance tests 2.5 and 7 months after diet onset, during the peri-menopausal and menopausal phases, respectively. Peri-menopause increased the severity of glucose intolerance and weight gain in middle-aged, HF-fed mice. Menopause increased weight gain in all mice regardless of age and diet, while chronological aging drove changes in adipose tissue distribution towards more visceral vs. subcutaneous adiposity. These data are in line with clinical data showing that post-menopausal women are more susceptible to metabolic dysfunction and suggest that greater chronological age exacerbates the effects of endocrine aging (menopause). This work highlights the importance of considering both chronological and endocrine aging in studies of metabolic health.
绝经加速代谢功能障碍,包括(前)糖尿病、肥胖和内脏脂肪堆积。然而,内分泌与年龄增长在这一过程中的影响尚不清楚。我们假设绝经,尤其是在中年时期,会加剧高脂肪饮食对代谢的影响。我们使用年轻成年和中年 C57BL/6J 雌性小鼠,通过长期给予高脂肪(HF)饮食或对照饮食来模拟饮食诱导的肥胖。我们通过注射 4-乙烯基环己烯二恶烷来模拟围绝经期/绝经,这会加速卵巢衰竭,而对照组则不会。我们在饮食开始后 2.5 和 7 个月进行了葡萄糖耐量试验,分别在围绝经期和绝经期间进行。围绝经期增加了中年 HF 喂养小鼠的葡萄糖耐量不良和体重增加的严重程度。绝经增加了所有小鼠的体重增加,无论年龄和饮食如何,而年龄增长导致脂肪组织分布向更多的内脏脂肪堆积转变。这些数据与临床数据一致,表明绝经后女性更容易出现代谢功能障碍,并表明更大的年龄增长加剧了内分泌衰老(绝经)的影响。这项工作强调了在代谢健康研究中考虑年龄增长和内分泌衰老的重要性。