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首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >A Functional Role for Nicotinic Acid Adenine Dinucleotide Phosphate in Oxytocin-Mediated Contraction of Uterine Smooth Muscle from Rat
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A Functional Role for Nicotinic Acid Adenine Dinucleotide Phosphate in Oxytocin-Mediated Contraction of Uterine Smooth Muscle from Rat

机译:烟酸腺嘌呤二核苷酸磷酸在催产素介导的大鼠子宫平滑肌收缩中的功能性作用

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摘要

Conventionally, G protein-coupled receptors are thought to increase calcium via inositol 1,4,5-trisphosphate (lnsP_3). More recent evidence shows that an alternative second messenger, nicotinic acid adenine dinucleotide phosphate (NAADP), also has a role to play, causing researchers to question established calcium releasing pathways. With the recent development, by our group, of cell-permeant NAADP (NAADP-aceteoxymethyl ester) and a selective NAADP receptor antagonist (Ned-19; 1-(3-((4-(2-fluorophenyl)piperazin-1-yl)methyl)-4-methoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylic acid), the ability to investigate this signaling pathway has improved. Therefore, we investigated a role for NAADP in oxytocin-medi-ated responses in the rat uterus. Oxytocin- and NAADP-medi-ated effects were investigated by using contractile measurements of whole uterine strips from rat in organ baths. Responses were correlated to calcium release in cultured rat uterine smooth muscle cells measured by fluorescence microscopy. Inhibition of both oxytocin-induced contraction and calcium release by the traditional NAADP-signaling disrupter bafilomycin and the NAADP receptor antagonist Ned-19 clearly demonstrated a role for NAADP in oxytocin-induced signaling. A cell-permeant form of NAADP was able to produce both uterine contractions and calcium release. This response was unaffected by depletion of sarcoplasmic reticulum stores with thapsigargin, but was abolished by both bafilomycin and Ned-19. Crucially, oxytocin stimulated an increase in NAADP in rat uterine tissue. The present study demonstrates directly that NAADP signaling plays a role in rat uterine contractions. Moreover, investigation of this signaling pathway highlights yet another component of oxytocin-mediated signaling, stressing the need to consider the action of new components as they are discovered, even in signaling pathways that are thought to be well established.
机译:通常,G蛋白偶联受体被认为通过肌醇1,4,5-三磷酸(InsP_3)增加钙。最近的证据表明,替代性的第二信使,烟酸腺嘌呤二核苷酸磷酸酯(NAADP)也起着作用,使研究人员质疑已建立的钙释放途径。随着我们小组对细胞渗透性NAADP(NAADP-乙酰氧基甲酯)和选择性NAADP受体拮抗剂(Ned-19; 1-(3-((4-(2-(2-氟苯基)哌嗪-1-基)甲基)-4-甲氧基苯基)-2,3,4,9-四氢-1H-吡啶并[3,4-b]吲哚-3-羧酸),提高了研究该信号通路的能力。因此,我们调查了NAADP在催产素介导的大鼠子宫反应中的作用。催产素和NAADP介导的作用是通过在器官浴中使用收缩测量大鼠全子宫条来研究的。通过荧光显微镜测量,反应与培养的大鼠子宫平滑肌细胞中的钙释放相关。传统NAADP信号破坏剂巴氟霉素和NAADP受体拮抗剂Ned-19对催产素诱导的收缩和钙释放的抑制作用清楚地证明了NAADP在催产素诱导的信号传导中的作用。 NAADP的细胞渗透形式能够产生子宫收缩和钙释放。该反应不受毒胡萝卜素耗尽肌质网贮存的影响,但被巴氟霉素和Ned-19均废除。至关重要的是,催产素刺激了大鼠子宫组织中NAADP的增加。本研究直接证明,NAADP信号传导在大鼠子宫收缩中起作用。此外,对该信号传导途径的研究突出了催产素介导的信号传导的另一个组成部分,强调了在发现新成分时就必须考虑其作用的必要性,即使是在公认的信号传导路径中也是如此。

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