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神经内分泌系统与免疫系统之间的新型联系:胃饥饿素免疫调节网络。

Novel connections between the neuroendocrine and immune systems: the ghrelin immunoregulatory network.

作者信息

Taub Dennis D

机构信息

Laboratory of Immunology, National Institute on Aging (NIH), Baltimore, MD 21224., USA.

出版信息

Vitam Horm. 2008;77:325-46. doi: 10.1016/S0083-6729(06)77014-5.

Abstract

There appears to be bidirectional communication between the neuroendocrine and immune systems. This communication is mediated by way of an array of cytokines, hormones, and neuropeptides. Inflammatory cytokines released by immune cells have been shown to act on the central nervous system to control food intake and energy homeostasis. Decrease in food intake or anorexia is one of the most common symptoms of illness, injury, or inflammation. The adipocyte-derived hormone, leptin, is considered a critical sensory anorexigenic mediator that signals to the brain changes in stored energy, determined by an altered balance between food intake and energy expenditure and has been shown to exert certain proinflammatory effects on immune cells. In contrast, ghrelin, the endogenous ligand for growth hormone secretagogue receptors (GHSRs), is produced primarily from stomach serving as a potent circulating orexigen controlling energy expenditure, adiposity, and GH secretion. However, the functional role of ghrelin and GHS in immune cell function remains unclear. Here, we review the current literature supporting a role for ghrelin in controlling inflammation and immunity and the potential therapeutic use of ghrelin and GHSR agonists in the management of inflammation and in restoration of thymic function in immunocompromised individuals.

摘要

神经内分泌系统和免疫系统之间似乎存在双向通信。这种通信是通过一系列细胞因子、激素和神经肽介导的。免疫细胞释放的炎性细胞因子已被证明可作用于中枢神经系统以控制食物摄入和能量平衡。食物摄入量减少或厌食是疾病、损伤或炎症最常见的症状之一。脂肪细胞衍生的激素瘦素被认为是一种关键的感觉性厌食介质,它向大脑发出储存能量变化的信号,这种变化由食物摄入和能量消耗之间的平衡改变所决定,并且已被证明对免疫细胞具有一定的促炎作用。相比之下,胃饥饿素是生长激素促分泌素受体(GHSRs)的内源性配体,主要由胃产生,是一种强效的循环食欲素,可控制能量消耗、肥胖和生长激素分泌。然而,胃饥饿素和生长激素促分泌素在免疫细胞功能中的作用仍不清楚。在此,我们综述了支持胃饥饿素在控制炎症和免疫中作用的当前文献,以及胃饥饿素和生长激素促分泌素受体激动剂在炎症管理和免疫功能低下个体胸腺功能恢复中的潜在治疗用途。

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