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首页> 外文期刊>Regulatory peptides. >Insulin-like growth factor-1 inhibits colonic smooth muscle cellapoptosis in diabetic rats with colonic dysmotility
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Insulin-like growth factor-1 inhibits colonic smooth muscle cellapoptosis in diabetic rats with colonic dysmotility

机译:胰岛素样生长因子-1抑制结肠功能性的糖尿病大鼠结肠平滑肌细胞凋亡

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摘要

Cellular apoptosis and colonic dysmotility are involved in diabetes mellitus (DM) complications. Insulin-likegrowth factor-1 (IGF-1) is known to affect apoptosis and proliferation. Here, we demonstrated that the treatmentof 1500 ng/kg IGF-1 partly recovers the decrease of the muscle thickness, body weight and gastrointestinal transitrate in DM rats. The gastrointestinal transit rate is positively correlated with the IGF-I level, but negativelycorrelated with the level of colonic cellular apoptosis. The DM-induced colonic apoptosis is also attenuated bythe IGF-1 stimulation. Moreover, IGF-1 inhibits the apoptosis of the isolated colonic SMCs in vitro via theactivation of PI3K/Akt and ERK1/2 signaling pathways. Taken together, our data indicated that IGF-1 inhibitsthe DM-induced colonic SMC apoptosis and might be involved in the alleviation of colonic dysmotility in diabeticrats.
机译:细胞凋亡和结肠功能性涉及糖尿病(DM)并发症。 已知胰岛素样胰岛素样系1(IGF-1)影响细胞凋亡和增殖。 在这里,我们证明了1500ng / kg IGF-1的处理部分地恢复了DM大鼠中肌厚度,体重和胃肠道碳碳的降低。 胃肠道传输速率与IGF-I水平正相关,但随着结肠细胞凋亡水平负相关。 DM诱导的结肠凋亡也通过IGF-1刺激衰减。 此外,IGF-1通过PI3K / AKT和ERK1 / 2信号传导途径的灭活来抑制分离的结肠SMC的凋亡。 我们的数据表明,IGF-1抑制DM诱导的结肠SMC细胞凋亡,并且可能参与减轻糖尿病患者的结肠功能性。

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