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胰升糖素样肽1受体激动剂与糖尿病、肥胖和银屑病 被引量:4

Glucagon-like peptide-1 receptor agonists, diabetes, obesity, and psoriasis
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摘要 肠促胰素治疗具有越来越多的胰外作用,最近有病例报道胰升糖素样肽1(GLP-1)受体激动剂治疗能缓解银屑病的临床症状。银屑病是以慢性炎症为特征的常见皮肤病变,流行病学研究发现银屑病患者的心血管疾病、肥胖和糖尿病的发生率增加,这可能与增加的局部和(或)全身的炎症有关。GLP-1受体激动剂可以通过直接或问接的机制影响免疫功能产生抗炎作用,从而改善银屑病症状,这为进一步研究肠促胰素的非经典的抗炎机制提供了新的切入点,同时对拓展GLP-1的临床应用也提供了一个新的研究方向。 More and more extrapancreatic actions of incretin-based therapies have been demonstrated and recently case reports have linked glucagon-like peptide-1 ( GLP-1 ) receptor agonist therapy with the improvements in psoriasis. Psoriasis is a common skin disorder characterized by chronic inflammation. Epideminological studies have showed that patients with psoriasis exhibit increased rates of cardiovascular disease, obesity, and type 2 diabetes, owing probably to the enhanced local and (or) systemic inflammation. The observations of anti-inflammatory actions of GLP-1, which exerts direct and indirect actions on immune function, together with the improved psoriasis, offer new insights into the investigation of non-classical anti-inflammatory actions of incretin-based therapeutics and provide a new direction for the research of the novel clinical application of GLP-1.
出处 《中华内分泌代谢杂志》 CAS CSCD 北大核心 2012年第4期255-257,共3页 Chinese Journal of Endocrinology and Metabolism
基金 上海市自然科学基金(11ZR1431900) 上海市卫生局课题(2011-301)
关键词 胰升糖素样肽1 银屑病 炎症 糖尿病 肥胖症 Glucagon-like peptide-1 Psoriasis Inflammation Diabetes mellitus Obesity
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参考文献18

  • 1Davidovici BB, Sattar N, Prinz JC, et al. Psoriasis and systemic inflammatory diseases: potential mechanistic links between skin disease and co-morbid conditions. J Invest Dermatol, 2010,130 : 1785-1796.
  • 2Hogan AE, Tobin AM, Ahem T, et al. Glueagun-like peptide-1 ( GLP- 1 ) and the regulation of human invariant natural killer T cells : lessons from obesity, diabetes and psoriasis. Diabetologia, 2011,54 : 2745- 2754.
  • 3Hadjiyanni I, Siminovitch KA, Danska JS, et al. Glucagon-like peptide-I receptor signalling selectively regulates murine lymphocyte proliferation and maintenance of peripheral regulatory T cells. Diabetologia, 2010,53:730-740.
  • 4Hadjiyanni I, Baggio LL, Poussier P, et al. Exendin-4 modulates diabetes onset in nonobese diabetic mice. Endocrinology, 2008,149 : 1338-1349.
  • 5Zhang J, Tokui Y, Yamagata K, et al. Continuous stimulation of human glucagon-like peptide-1 (7-36) amide in a mouse model (NOD) delays onset of autoimmune type 1 diabetes. Diabetologia, 2007,50 : 1900- 1909.
  • 6Marx N, Burgmaier M, Heinz P, et al. Glucagon-like peptide-1 ( 1 ~37 ) inhibits chemokine-induced migration of human CD4-positive lymphocytes. Cell Mol Life Sci, 2010,67:3549-3555.
  • 7Libby PJ, Plutzky J. Inflammation in diabetes mellitus: role of peroxisome proliferator-activated receptor-alpha and peroxisome proliferator-activated receptor-gamma agonists. Am J Cardiol, 2007, 99:27B40B.
  • 8Sertznig P, Seifert M, Tilgen W, et al. Peroxisome proliferator- activated receptors (PPARs) and the human skin: importance of PPARs in skin physiology and dermatologic diseases. Am J Clin Dermatol, 2008,9 : 15-31.
  • 9Mittal R, Malhotra S, Pandhi P, et al. Efficacy and safety of combination Acitretin and Pioglitazone therapy in patients with moderate to severe chronic plaque-type psoriasis: a randomized, double-blind, placebo-controlled clinical trial. Arch Dermatol, 2009,145:387-393.
  • 10List JF, He H, Habener JF. Glucagon-like peptide-1 receptor and proglucagon expression in mouse skin. Regul Pept, 2006, 134: 149- 157.

同被引文献18

  • 1刘展.1例银屑病合并糖尿病感染患者的护理[J].吉林医学,2005,26(5):543-544. 被引量:6
  • 2中华医学会糖尿病学分会.中国2型糖尿病防治指南(2010年版).中华糖尿病杂志,2010,3增刊2:1-56.
  • 3Bullo-Bonet M, Garcia-Lorda P, Lopez-Soriano FJ, et al. Tumour necrosis factor, a key role in obesity?. FEBS Lett, 1999, 451: 215-219.
  • 4Moller DE. Potential role of TNF-alpha in the pathogenesis of insulin resistance and type 2 diabetes. Trends Endocrinol Metab, 2000, 11:212-217.
  • 5Heine R J, Van Gaal LF, Johns D, et al. Exenatide versus insulin glargine in patients with suboptimally controlled type 2 diabetes:a randomized trial. Ann Intern Med, 2005, 143:559-569.
  • 6Nauck MA, Duran S, Kim D, et al. A comparison of twice-daily exenatide and biphasic insulin aspart in patients with type 2 diabetes who were suboptimally controlled with sulfonylurea and meffomtin :a non-inferiority study. Diabetologia, 2007, 50:259-267.
  • 7Klonoff DC, Buse JB, Nielsen LL, et al. Exenatide effects on diabetes, obesity, cardiovascular risk factors and hepatic biomarkers in patients with type 2 diabetes treated for 3 years. Curr Med Res Opin, 2008, 24:275-286.
  • 8McCall AL, Cox DJ, Brodows R, et al. Reduced daily risk of glycemic variability : comparison of exenatide with insulin glargine. Diabetes Technol Ther,2009, 11:339-344.
  • 9Kesavadev J, Shankar A, Krishnan G, et al. Liraglutide therapy beyond glycemic control:an observational study in Indian patients with type 2 diabetes in real world setting. Int J Gen Med,2012,5 : 317 -322.
  • 10Kim Chung le T, Hosaka T, Yoshida M, et al. Exendin-4, a GLP-1 receptor agonist, directly induces adiponectin expression through protein kinase A pathway and prevents inflammatory adipokinc expression. Biochem Biopbys Res Commun, 2009, 390:613-618.

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