Li Shuguang, Li Yixiang, Xiang Lin, Dong Jing, Liu Min, Xiang Guangda
Department of Endocrinology, Wuhan General Hospital of Guangzhou Command, Wuluo Road 627, Wuhan 430070, Hubei Province, China.
Department of Hematology and Medical Oncology, School of Medicine, Emory University, Atlanta, GA 30322, USA.
Metabolism. 2018 Jan;78:106-117. doi: 10.1016/j.metabol.2017.09.008. Epub 2017 Oct 3.
To investigate that short-term treatment of sildenafil can induce browning of subcutaneous white adipose tissue (sWAT) in human adults.
A randomized, double-blinded, placebo-controlled, parallel group trial.
Sixteen eligibility overweight male subjects were recruited, comparing 100mg/day sildenafil versus an identical placebo therapy for 7days. sWAT samples were collected from subjects before and after 7-day sildenafil or placebo interventions.
The results showed that multilocular UCP1-positive adipocytes existed in sWAT samples from subjects after sildenafil treatment. Compared to before treatment in both group as well as after treatment in placebo, sildenafil significantly decreased adipocyte size, increased the expressions of UCP1 protein and mRNA, mitochondrial density, and leak respiratory capacity in sWAT (p<0.05). Sildenafil also increased plasma cyclic guanosine-3',5'-monophosphate (cGMP) and catecholamine concentrations (p<0.05), and consequently activated the expressions of vasodilator-stimulated phosphoprotein (VASP) and p70 ribosomal S6 kinase 1 (S6K1) (p<0.05). Sildenafil did not activate typical brown fat.
The current findings demonstrate that sildenafil can induce browning of sWAT in human, and this action may be through cGMP-dependent protein kinase I and mechanistic/mammalian target of rapamycin (mTOR) signaling pathways. Sldenafil may be a promising treatment for metabolic disease.
研究西地那非短期治疗能否诱导成年人体内皮下白色脂肪组织(sWAT)棕色化。
一项随机、双盲、安慰剂对照、平行组试验。
招募了16名符合条件的超重男性受试者,比较每天100毫克西地那非与相同的安慰剂治疗7天的效果。在西地那非或安慰剂干预7天前后采集受试者的sWAT样本。
结果显示,西地那非治疗后受试者的sWAT样本中存在多泡UCP1阳性脂肪细胞。与两组治疗前以及安慰剂治疗后相比,西地那非显著减小了脂肪细胞大小,增加了sWAT中UCP1蛋白和mRNA的表达、线粒体密度以及漏呼吸能力(p<0.05)。西地那非还增加了血浆环磷酸鸟苷(cGMP)和儿茶酚胺浓度(p<0.05),从而激活了血管舒张刺激磷蛋白(VASP)和p70核糖体S6激酶1(S6K1)的表达(p<0.05)。西地那非未激活典型的棕色脂肪。
目前的研究结果表明,西地那非可诱导人体sWAT棕色化,且这一作用可能通过cGMP依赖性蛋白激酶I和雷帕霉素机制性/哺乳动物靶点(mTOR)信号通路实现。西地那非可能是一种有前景的代谢疾病治疗药物。