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本文引用的文献

1
Cytokine-induced alterations of gastrointestinal motility in gastrointestinal disorders.细胞因子诱导的胃肠道疾病中胃肠动力改变
World J Gastrointest Pathophysiol. 2011 Oct 15;2(5):72-81. doi: 10.4291/wjgp.v2.i5.72.
2
Ghrelin attenuates gastrointestinal epithelial damage induced by doxorubicin.Ghrelin 可减轻多柔比星引起的胃肠道上皮损伤。
World J Gastroenterol. 2011 Sep 7;17(33):3836-41. doi: 10.3748/wjg.v17.i33.3836.
3
Ghrelin receptors are expressed by distal tubules of the mouse kidney.胃饥饿素受体在小鼠肾脏的远曲小管表达。
Cell Tissue Res. 2011 Oct;346(1):135-9. doi: 10.1007/s00441-011-1240-4. Epub 2011 Sep 29.
4
Human ghrelin protects animals from renal ischemia-reperfusion injury through the vagus nerve.人类生长激素通过迷走神经保护动物免受肾缺血再灌注损伤。
Surgery. 2012 Jan;151(1):37-47. doi: 10.1016/j.surg.2011.06.027. Epub 2011 Sep 22.
5
Use of ghrelin as a treatment for inflammatory bowel disease: mechanistic considerations.胃饥饿素作为炎症性肠病治疗方法的应用:机制探讨
Int J Pept. 2011;2011:189242. doi: 10.1155/2011/189242. Epub 2011 Aug 9.
6
Fall in plasma ghrelin concentrations after cisplatin-based chemotherapy in esophageal cancer patients.食管癌患者顺铂化疗后血浆 ghrelin 浓度下降。
Int J Clin Oncol. 2012 Aug;17(4):316-23. doi: 10.1007/s10147-011-0289-0. Epub 2011 Jul 20.
7
Myths and truths of growth hormone and testosterone therapy in heart failure.心力衰竭中生长激素和睾酮治疗的误区与真相
Expert Rev Cardiovasc Ther. 2011 Jun;9(6):711-20. doi: 10.1586/erc.11.25.
8
Attenuation of muscle atrophy by an N-terminal peptide of the receptor for proteolysis-inducing factor (PIF).蛋白水解诱导因子(PIF)受体 N 端肽抑制肌肉萎缩。
Br J Cancer. 2011 Jun 28;105(1):83-8. doi: 10.1038/bjc.2011.216. Epub 2011 Jun 14.
9
The obesity paradox in heart failure: accepting reality and making rational decisions.心力衰竭中的肥胖悖论:接受现实并做出理性决策。
Clin Pharmacol Ther. 2011 Jul;90(1):188-90. doi: 10.1038/clpt.2011.72. Epub 2011 Jun 8.
10
Use of orexigenic medications in geriatric patients.老年患者中食欲促进药物的使用。
Am J Geriatr Pharmacother. 2011 Apr;9(2):97-108. doi: 10.1016/j.amjopharm.2011.04.001.

生长激素释放肽及生长激素释放肽受体激动剂治疗疾病动物模型的作用:疗效和机制。

The use of ghrelin and ghrelin receptor agonists as a treatment for animal models of disease: efficacy and mechanism.

机构信息

Department of Pediatrics, Division of Pediatric Endocrinology, University of Virginia, P.O. Box 800386, Charlottesville, VA 22908, USA.

出版信息

Curr Pharm Des. 2012;18(31):4779-99. doi: 10.2174/138161212803216951.

DOI:10.2174/138161212803216951
PMID:22632859
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6076443/
Abstract

Ghrelin is a stomach-derived hormone that acts at the ghrelin receptor (formerly called the Growth Hormone Secretagogue (GHS)-1a receptor) in multiple tissues throughout the body, exhibiting pleotropic effects potentially beneficial as a treatment in human disease states. Given its properties including increasing appetite, decreasing systemic inflammation, decreasing vascular resistance, increasing cardiac output, and increasing growth hormone and IGF-1 levels, ghrelin has been tested as a treatment in animal models of multiple disease states that produce the deficits in these processes. Thus, the efficacy of ghrelin has been testing in diseases involving anorexia, negative energy balance, cardiovascular compromise, systemic inflammation and gastroparesis. These diseases include cancer cachexia, chronic heart failure, chronic renal failure, chemotherapy, arthritis, gastroparesis and inflammatory bowel disease. Across this wide variety of diseases treatment with ghrelin and ghrelin agonists have produced benefits, though given ghrelin's widespread effects, the exact mechanisms behind ghrelin's action in these settings is frequently difficult to determine. Further investigation using animal models may help to determine mechanisms that are most operative in these disease states and narrow treatment parameters helpful for human application.

摘要

胃饥饿素是一种由胃分泌的激素,作用于全身多个组织中的胃饥饿素受体(以前称为生长激素促分泌素 1a 受体),具有多种潜在有益的作用,可作为人类疾病状态的治疗方法。鉴于其增加食欲、减少全身炎症、降低血管阻力、增加心输出量以及增加生长激素和 IGF-1 水平等特性,胃饥饿素已在多种产生这些过程缺陷的疾病动物模型中进行了治疗测试。因此,胃饥饿素在涉及厌食症、负能量平衡、心血管功能障碍、全身炎症和胃轻瘫的疾病中的疗效已得到检验。这些疾病包括癌症恶病质、慢性心力衰竭、慢性肾衰竭、化疗、关节炎、胃轻瘫和炎症性肠病。在这一系列广泛的疾病中,使用胃饥饿素和胃饥饿素激动剂进行治疗已产生了益处,尽管鉴于胃饥饿素的广泛作用,在这些情况下确定胃饥饿素作用的确切机制通常很困难。使用动物模型的进一步研究可能有助于确定在这些疾病状态中最有效的机制,并缩小有助于人类应用的治疗参数。