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注射磷脂酰胆碱和脱氧胆酸可调节脂肪组织中脂肪分解相关因子、促炎细胞因子和激素的基因表达。

Injection of phosphatidylcholine and deoxycholic acid regulates gene expression of lipolysis-related factors, pro-inflammatory cytokines, and hormones on mouse fat tissue.

机构信息

Laboratory of Host Defense Modulation, College of Pharmacy, Chung-Ang University, Seoul 156-756, Republic of Korea.

出版信息

Food Chem Toxicol. 2013 Oct;60:263-8. doi: 10.1016/j.fct.2013.07.057. Epub 2013 Jul 30.

Abstract

Injection of phosphatidylcholine (PC) and deoxycholic acid (DA) preparation is widely used as an alternative to liposuction for the reduction of subcutaneous fat. Nevertheless, its physiological effects and mechanism of action are not yet fully understood. In this report, PC and deoxycholic acid (DA) were respectively injected into adipose tissue. PC decreased tissue mass on day 7, but DA did not. On the other hand, a decrement of DNA mass was observed only in DA-injected tissue on day 7. Both PC and DA reduced the mRNA expression of adipose tissue hormones, such as adiponectin, leptin, and resistin. In lipolysis-related gene expression profiles, PC increased hormone-sensitive lipase (HSL) transcription and decreased the expression other lipases, perilipin, and the lipogenic marker peroxisome proliferator-activated receptor-γ (PPARγ); DA treatment diminished them all, including HSL. Meanwhile, the gene expression of pro-inflammatory cytokines and a chemokine was greatly elevated in both PC-injected and DA-injected adipose tissue. Microscopic observation showed that PC induced lipolysis with mild PMN infiltration on day 7. However, DA treatment did not induce lipolysis but induced much amount of PMN infiltration. In conclusion, PC alone might induce lipolysis in adipose tissue, whereas DC alone might induce tissue damage.

摘要

注射磷脂酰胆碱(PC)和脱氧胆酸(DA)制剂被广泛用作吸脂术的替代方法,用于减少皮下脂肪。然而,其生理作用和作用机制尚未完全了解。在本报告中,分别将 PC 和脱氧胆酸(DA)注入脂肪组织。PC 在第 7 天减少了组织质量,但 DA 没有。另一方面,仅在第 7 天的 DA 注射组织中观察到 DNA 质量的减少。PC 和 DA 均降低了脂肪组织激素的 mRNA 表达,如脂联素、瘦素和抵抗素。在脂肪分解相关基因表达谱中,PC 增加了激素敏感脂肪酶(HSL)的转录,降低了其他脂肪酶、脂滴蛋白和脂肪生成标志物过氧化物酶体增殖物激活受体-γ(PPARγ)的表达;DA 处理降低了所有这些表达,包括 HSL。同时,PC 注射和 DA 注射的脂肪组织中促炎细胞因子和趋化因子的基因表达显著升高。显微镜观察显示,PC 在第 7 天诱导脂肪分解并伴有轻度中性粒细胞浸润。然而,DA 处理并未诱导脂肪分解,而是诱导了大量中性粒细胞浸润。总之,PC 单独可能诱导脂肪组织中的脂肪分解,而 DA 单独可能诱导组织损伤。

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