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Nitric oxide in the bovine oviduct: Influence on contractile activity and nitric oxide synthase isoforms localization

机译:牛输卵管中的一氧化氮:对收缩活性和一氧化氮合酶同工型定位的影响

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The oviducts of 64 Holstein cows in luteal (early I, early II and late) and follicular phases were evaluated to determine the protein expression and mRNA transcription of different nitric oxide synthase isoforms (eNOS, iNOS, nNOS) as well as the effect of nitric oxide (NO) on spontaneous contractility in vitro. The expression patterns of nitric oxide synthase (NOS) isoforms in isthmus and ampulla (n = 6 for each phase) were determined by immunohistochemistry, reverse transcriptase polymerase chain reaction (RT-PCR) and Western blot analysis. In the contractility studies, longitudinal and circular isolated strips of isthmus and ampulla (n = 10 for each phase) of oviducts located ipsilateral to the luteal structure or preovulatory follicle were treated as follows: a) L-arginine, an endogenous NO donor (10(-8) to 10(-3) M), b) N-omega-nitro-L-arginine methyl ester (L-NAME), a NOS inhibitor (10(-5) M) and L-arginine (10(-3) M), c) methylene blue (MB), an inhibitor of soluble guanylate (10(-5) M) and L-arginine (10(-3) M) and d) sodium nitroprusside (SNP), an exogenous NO donor (10(-8) to 10(-4) M). Immunohistochemical evaluation revealed that endothelial NOS (eNOS) expression detected in epithelial layer of isthmus and ampulla was strong in early I luteal phase, moderate in follicular phase and weak in other phases. Neuronal NOS (nNOS) irnmunoreactivity was strong in isthmus and moderate in ampulla, and staining of nerve fibers was observed mostly in early I luteal and follicular phases. All eNOS, nNOS and inducible NOS (iNOS) isoforms were detected by RT-PCR. eNOS and iNOS proteins were evident, whereas nNOS was undetectable by Western blot analysis in the tissue examined. L-arginine applied alone or after L-NAME did not alter or increase the contractile tension of the strips in most tissues examined. However, L-arginine applied after MB increased contractile tension in the strips of ampulla and longitudinal isthmus from early I luteal phase and circular isthmus from follicular phase but decreased it in isthmus from early 11 luteal phase. SNP differentially modulated oviductal contraction depending on the type of muscular strips and period examined. These results showed the estrous phase-dependent changes related to endogenous NO system which might be of physiological importance to the oviduct for secretory and ciliary functions involved in gametes and embryo(s) transportation. (C) 2012 Elsevier Inc. All rights reserved.
机译:评价了黄体期(早期I,早期II和晚期)和卵泡期的64头荷斯坦奶牛的输卵管,以确定不同一氧化氮合酶同工型(eNOS,iNOS,nNOS)的蛋白质表达和mRNA转录以及硝酸的影响氧化物(NO)对体外自发收缩力的影响。通过免疫组织化学,逆转录酶聚合酶链反应(RT-PCR)和蛋白质印迹分析确定峡部和壶腹中一氧化氮合酶(NOS)亚型的表达模式(每相n = 6)。在收缩性研究中,对位于黄体结构或排卵前卵泡同侧的输卵管的纵向和圆形隔离的峡部和壶腹部带(每相n = 10)进行如下处理:a)L-精氨酸,一种内源性NO供体(10 (-8)至10(-3)M),b)N-ω-硝基-L-精氨酸甲酯(L-NAME),NOS抑制剂(10(-5)M)和L-精氨酸(10( -3)M),c)亚甲基蓝(MB),可溶性鸟嘌呤(10(-5)M)和L-精氨酸(10(-3)M)的抑制剂,d)亚硝普钠(SNP),一种外源性抑制剂没有供体(10(-8)至10(-4)M)。免疫组织化学评估显示,在峡部和壶腹部上皮层中检测到的内皮NOS(eNOS)表达在I黄体早期很强,在卵泡期中等,而在其他阶段则较弱。峡部神经元NOS(nNOS)免疫反应性强,壶腹中度,中度黄体期和卵泡期主要观察到神经纤维染色。通过RT-PCR检测所有eNOS,nNOS和诱导型NOS(iNOS)同工型。 eNOS和iNOS蛋白很明显,而通过蛋白质印迹分析无法在检测的组织中检测到nNOS。在大多数检查的组织中,单独或在L-NAME后使用L-精氨酸不会改变或增加试纸条的收缩张力。然而,MB后应用L-精氨酸可增加壶腹期壶腹和纵向峡部条带的收缩张力,从卵泡期开始的峡部峡部的环形峡部收缩,但从11期黄体期的峡部则降低其张力。 SNP根据肌肉条的类型和所检查的时期来差异调节输卵管收缩。这些结果表明,与内源性NO系统有关的发情阶段依赖性变化可能对输卵管的生理性重要性,该输卵管对于参与配子和胚胎运输的分泌和纤毛功能具有重要意义。 (C)2012 Elsevier Inc.保留所有权利。

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