Nonogaki Katsunori, Nozue Kana, Oka Yoshitomo
Center of Excellence, Division of Molecular Metabolism and Diabetes, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Japan.
Biochem Biophys Res Commun. 2006 Dec 29;351(4):1078-82. doi: 10.1016/j.bbrc.2006.10.173. Epub 2006 Nov 7.
Serotonin (5-hydroxytryptamine; 5-HT) 2A receptors contribute to the effects of 5-HT on platelet aggregation and vascular smooth muscle cell proliferation, and are reportedly involved in decreases in plasma levels of adiponectin, an adipokine, in diabetic subjects. Here, we report that systemic administration of sarpogrelate, a 5-HT2A receptor antagonist, suppressed appetite and increased hypothalamic pro-opiomelanocortin and cocaine- and amphetamine-regulated transcript, corticotropin releasing hormone, 5-HT2C, and 5-HT1B receptor gene expression. A(y) mice, which have ectopic expression of the agouti protein, significantly increased hypothalamic 5-HT2A receptor gene expression in association with obesity compared with wild-type mice matched for age. Systemic administration of sarpogrelate suppressed overfeeding, body weight gain, and hyperglycemia in obese A(y) mice, whereas it did not increase plasma adiponectin levels. These results suggest that obesity increases hypothalamic 5-HT2A receptor gene expression, and pharmacologic inactivation of 5-HT2A receptors inhibits overfeeding and obesity in A(y) mice, but did not increase plasma adiponectin levels.
血清素(5-羟色胺;5-HT)2A受体参与5-HT对血小板聚集和血管平滑肌细胞增殖的作用,据报道还与糖尿病患者体内脂肪因子脂联素血浆水平降低有关。在此,我们报告5-HT2A受体拮抗剂沙格雷酯的全身给药可抑制食欲,并增加下丘脑阿黑皮素原、可卡因和安非他明调节转录物、促肾上腺皮质激素释放激素、5-HT2C和5-HT1B受体基因的表达。与年龄匹配的野生型小鼠相比,异位表达刺鼠蛋白的A(y)小鼠与肥胖相关的下丘脑5-HT2A受体基因表达显著增加。沙格雷酯的全身给药可抑制肥胖A(y)小鼠的过度进食、体重增加和高血糖,而不会增加血浆脂联素水平。这些结果表明,肥胖会增加下丘脑5-HT2A受体基因表达,5-HT2A受体的药理学失活可抑制A(y)小鼠的过度进食和肥胖,但不会增加血浆脂联素水平。