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The effects of second messenger cAMP and its relative components on the contraction of uterine smooth muscle of rat

机译:第二信使cAMP及其相关成分对大鼠子宫平滑肌收缩的影响

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OBJECTIVE: To investigate the effect of second messenger pathways on the uterine smooth muscle contraction and their associated mechanisms, and compare the evaluation methods. MATERIALS AND METHODS: Preparation of uterine smooth muscle strips from healthy pregnant 18-21 d SD and non-pregnant rats. When the contraction of muscle strips was stable, we conducted gradient administration: PDE4 inhibitors (Z90), prostaglandin PGE2, adenylate cyclase inhibitor (SQ 22,530), cAMP analogs (dbcAMP) and AMPK agonists (AICAR), solvent dimethyl sulfoxide (DMSO) as controlled. Gradient administration of acetylcholine (Ach) and oxytocin (oxytocin) induced the contraction of muscle strips. The tension transducer and biological information collecting system were applied to record the changes, including duration, dilation tension, contraction tension, peak height, and mean tension, before and after different administration. Principal components analysis was adopted to evaluate the five changes. RESULTS: SQ 22,530, DMSO, cAMP alone had no significant effect on the contraction of uterine smooth muscle; Z90 can inhibit the spontaneous contraction of pregnant uterine smooth muscle strips; dbcAMP and AICAR can antagonize acetylcholine and oxytocin-induced the contraction of pregnant uterine smooth muscle strips. Z90, SQ 22,530 + Z90, dbcAMP, AICAR can inhibit the uterine contraction peak, diastolic amplitude, average muscle tone and contraction duration of the pregnant uterine smooth muscle in a concentration-dependent manners. At the same time, we compared the parameters, which reflect the contraction of uterine smooth muscle, and conduct main components analysis to determine the effect of the drugs. CONCLUSIONS: The second messenger cAMP and its related components ATP, 5’- AMP, AC, PDE, PKA, and AMPK can affect the uterine smooth muscle contraction via related signaling pathway in rats, and principal components analysis can be adopted to evaluate the smooth muscle relaxant.
机译:目的:探讨第二信使通路对子宫平滑肌收缩的影响及其相关机制,并比较评价方法。材料与方法:从健康的孕妇18-21 d SD和非妊娠大鼠制备子宫平滑肌条。当肌肉条的收缩稳定时,我们进行梯度给药:PDE4抑制剂(Z90),前列腺素PGE2,腺苷酸环化酶抑制剂(SQ 22,530),cAMP类似物(dbcAMP)和AMPK激动剂(AICAR),溶剂二甲基亚砜(DMSO)受控。乙酰胆碱(Ach)和催产素(oxytocin)的梯度给药引起了肌肉条的收缩。应用张力传感器和生物信息收集系统记录不同给药前后的变化,包括持续时间,扩张张力,收缩张力,峰高和平均张力。通过主成分分析来评估这五个变化。结果:单独的SQ 22,530,DMSO,cAMP对子宫平滑肌的收缩没有显着影响。 Z90可以抑制孕妇子宫平滑肌条的自发收缩; dbcAMP和AICAR可以拮抗乙酰胆碱和催产素引起的孕妇子宫平滑肌条的收缩。 Z90,SQ 22,530 + Z90,dbcAMP,AICAR可以浓度依赖的方式抑制妊娠子宫平滑肌的子宫收缩峰,舒张幅度,平均肌张力和收缩持续时间。同时,我们比较了反映子宫平滑肌收缩的参数,并进行了主要成分分析以确定药物的作用。结论:第二信使cAMP及其相关成分ATP,5'-AMP,AC,PDE,PKA和AMPK可通过相关信号通路影响大鼠子宫平滑肌收缩,可采用主成分分析法评价平滑度肌肉松弛剂。

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