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食欲素在葡萄糖稳态调节中的作用。

Role of orexin in the regulation of glucose homeostasis.

机构信息

Department of Clinical Pharmacology, University of Toyama, Toyama, Japan.

出版信息

Acta Physiol (Oxf). 2010 Mar;198(3):335-48. doi: 10.1111/j.1748-1716.2009.02008.x. Epub 2009 May 28.

Abstract

Orexin-A (hypocretin-1) and orexin-B (hypocretin-2) are hypothalamic neuropeptides that play key roles in the regulation of wakefulness, feeding, reward, autonomic functions and energy homeostasis. To control these functions indispensable for survival, orexin-expressing neurones integrate peripheral metabolic signals, interact with many types of neurones in the brain and modulate their activities via the activation of orexin-1 receptor or orexin-2 receptor. In addition, a new functional role of orexin is emerging in the regulation of insulin and leptin sensitivities responsible for whole-body glucose metabolism. Recent evidence indicates that orexin efficiently protects against the development of peripheral insulin resistance induced by ageing or high-fat feeding in mice. In particular, the orexin receptor-2 signalling appears to confer resistance to diet-induced obesity and insulin insensitivity by improving leptin sensitivity. In fact, the expression of orexin gene is known to be down-regulated by hyperglycaemia in the rodent model of diabetes, such as ob/ob and db/db mice. Moreover, the levels of orexin receptor-2 mRNA have been shown to decline in the brain of mice along with ageing. These suggest that hyperglycaemia due to insulin insensitivity during ageing or by habitual consumption of a high-fat diet leads to the reduction in orexin expression in the hypothalamus, thereby further exacerbating peripheral insulin resistance. Therefore, orexin receptor controlling hypothalamic insulin/leptin actions may be a new target for possible future treatment of hyperglycaemia in patients with type 2 diabetes.

摘要

食欲素-A(下丘脑分泌素-1)和食欲素-B(下丘脑分泌素-2)是下丘脑神经肽,在调节觉醒、摄食、奖赏、自主功能和能量稳态方面发挥着关键作用。为了控制这些对生存至关重要的功能,表达食欲素的神经元整合外周代谢信号,与大脑中的许多类型的神经元相互作用,并通过激活食欲素-1 受体或食欲素-2 受体来调节它们的活动。此外,食欲素在调节胰岛素和瘦素敏感性方面的新功能作用正在出现,这些敏感性负责全身葡萄糖代谢。最近的证据表明,食欲素能有效地防止衰老或高脂肪喂养引起的小鼠外周胰岛素抵抗的发展。特别是,食欲素受体-2 信号似乎通过改善瘦素敏感性来赋予对饮食诱导肥胖和胰岛素不敏感的抵抗力。事实上,已知在糖尿病啮齿动物模型(如 ob/ob 和 db/db 小鼠)中,高血糖会下调食欲素基因的表达。此外,研究还表明,随着年龄的增长,食欲素受体-2 mRNA 的水平在小鼠大脑中下降。这表明,衰老过程中由于胰岛素不敏感或习惯性摄入高脂肪饮食导致的高血糖会导致下丘脑食欲素表达减少,从而进一步加重外周胰岛素抵抗。因此,控制下丘脑胰岛素/瘦素作用的食欲素受体可能是治疗 2 型糖尿病患者高血糖的新靶点。

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