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用于诱导脂肪分解和治疗脂肪团的中胚层疗法溶液的评估。

An evaluation of mesotherapy solutions for inducing lipolysis and treating cellulite.

作者信息

Caruso Mary K, Roberts Andrew T, Bissoon Lionel, Self K Stan, Guillot Thomas S, Greenway Frank L

机构信息

Louisiana State University, Department of Human Ecology, Baton Rouge, LA 70803, USA.

出版信息

J Plast Reconstr Aesthet Surg. 2008 Nov;61(11):1321-4. doi: 10.1016/j.bjps.2007.03.039. Epub 2007 Oct 22.

Abstract

The aim of this study was to evaluate the lipolytic potential of solutions used in the practice of cosmetic mesotherapy to stimulate lipolysis, cause local fat reduction and reduce the appearance of cellulite. The mesotherapy solutions were tested in a human fat cell assay using the fold induction of glycerol generation as a measure of lipolysis. The following mesotherapy solutions were tested: aminophylline; yohimbine; isoproterenol; melilotus; aminophylline with melilotus; aminophylline with isoproterenol; aminophylline with isoproterenol and yohimbine; aminophylline with isoproterenol and lidocaine; and aminophylline with isoproterenol, yohimbine and lidocaine. Isoproterenol (P<0.002), aminophylline (P<0.00004) and yohimbine (P<0.001) stimulated lipolysis compared to the buffer control. The lipolysis stimulated by melilotus (P<0.01) and isoproterenol (P<0.002) was enhanced by aminophylline (P<0.001 and P<0.001, respectively). The lipolytic stimulation by aminophylline and isoproterenol (P<0.0009), and by aminophylline and isoproterenol with yohimbine (P<0.0007) was inhibited by lidocaine, not significant compared to buffer control for aminophylline and isoproterenol, but aminophylline, isoproterenol and yohimbine still stimulated lipolysis more than control, P<0.05). Isoproterenol, aminophylline, yohimbine and melilotus stimulate lipolysis alone, and lipolysis is further enhanced by combining lipolytic stimulators in mesotherapy solutions. Lidocaine is antilipolytic and should be removed from mesotherapy solutions designed for local fat reduction.

摘要

本研究的目的是评估用于美容中胚层疗法实践的溶液的脂解潜力,以刺激脂肪分解、减少局部脂肪并减少橘皮组织的外观。在人体脂肪细胞试验中,以甘油生成的倍数诱导作为脂解的指标,对中胚层疗法溶液进行了测试。测试了以下中胚层疗法溶液:氨茶碱;育亨宾;异丙肾上腺素;草木犀;氨茶碱与草木犀;氨茶碱与异丙肾上腺素;氨茶碱与异丙肾上腺素和育亨宾;氨茶碱与异丙肾上腺素和利多卡因;以及氨茶碱与异丙肾上腺素、育亨宾和利多卡因。与缓冲液对照相比,异丙肾上腺素(P<0.002)、氨茶碱(P<0.00004)和育亨宾(P<0.001)刺激了脂解。氨茶碱分别增强了草木犀(P<0.01)和异丙肾上腺素(P<0.002)刺激的脂解(分别为P<0.001和P<0.001)。利多卡因抑制了氨茶碱和异丙肾上腺素(P<0.0009)以及氨茶碱和异丙肾上腺素与育亨宾(P<0.0007)的脂解刺激,与氨茶碱和异丙肾上腺素的缓冲液对照相比不显著,但氨茶碱、异丙肾上腺素和育亨宾仍比对照更能刺激脂解(P<0.05)。异丙肾上腺素、氨茶碱、育亨宾和草木犀单独刺激脂解,并且在中胚层疗法溶液中组合脂解刺激剂可进一步增强脂解。利多卡因具有抗脂解作用,应从用于局部减脂的中胚层疗法溶液中去除。

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