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一氧化氮合酶在雄性大鼠生殖器官中的定位

Localization of nitric oxide synthase in the reproductive organs of the male rat.

作者信息

Burnett A L, Ricker D D, Chamness S L, Maguire M P, Crone J K, Bredt D S, Snyder S H, Chang T S

机构信息

Department of Urology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287.

出版信息

Biol Reprod. 1995 Jan;52(1):1-7. doi: 10.1095/biolreprod52.1.1.

Abstract

Nitric oxide synthase (NOS), which catalyzes the production of nitric oxide (NO), was characterized within the reproductive tract of adult male Sprague-Dawley rats by means of biochemical and immunohistochemical techniques. Tissues examined included the testis, epididymis (caput, corpus, and cauda regions), vas deferens, ejaculatory duct, seminal vesicle, and coagulating gland. NOS activity was measured by use of an assay based on the stoichiometric conversion of [3H]-L-arginine to [3H]-L-citrulline and NO, catalyzed by NOS. Low levels of NOS activity were detected in the testis and seminal vesicle (< 0.5 fmol [3H]-L-citrulline formed/min/mg protein in each tissue). The highest levels of NOS activity were present in the cauda segment of the epididymis and in the vas deferens, each having a sevenfold greater amount of NOS activity than the testis (p < 0.05). Intermediate levels of NOS activity were detected in the coagulating gland (0.863 +/- 0.248 fmol [3H]-L-citrulline formed/min/mg protein), caput epididymidis (0.457 +/- 0.180 fmol [3H]-L-citrulline formed/min/mg protein), and corpus epididymidis (0.631 +/- 0.215 fmol [3H]-L-citrulline formed/min/mg protein). NADPH diaphorase histochemistry and NOS immunohistochemistry localized NOS to neuronal fibers coursing throughout the smooth musculature and subepithelial regions of the epididymis, vas deferens, and ejaculatory duct. Endothelial cells and nerve plexuses within the adventitia of blood vessels supplying reproductive tissues were also positive for NOS. Additional localizations of NOS were within epithelial cells of the epididymis and coagulating gland.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

一氧化氮合酶(NOS)可催化一氧化氮(NO)的生成,本研究采用生化和免疫组化技术对成年雄性斯普拉格-道利大鼠生殖道内的该酶进行了特性分析。所检测的组织包括睾丸、附睾(头、体和尾段)、输精管、射精管、精囊和凝固腺。通过基于[3H]-L-精氨酸经NOS催化化学计量转化为[3H]-L-瓜氨酸和NO的检测方法来测定NOS活性。在睾丸和精囊中检测到较低水平的NOS活性(每个组织中形成的[3H]-L-瓜氨酸<0.5 fmol/分钟/毫克蛋白质)。NOS活性最高的部位是附睾尾段和输精管,其NOS活性比睾丸高7倍(p<0.05)。在凝固腺(0.863±0.248 fmol[3H]-L-瓜氨酸形成/分钟/毫克蛋白质)、附睾头(0.457±0.180 fmol[3H]-L-瓜氨酸形成/分钟/毫克蛋白质)和附睾体(0.631±0.215 fmol[3H]-L-瓜氨酸形成/分钟/毫克蛋白质)中检测到中等水平的NOS活性。NADPH黄递酶组织化学和NOS免疫组化将NOS定位于贯穿附睾、输精管和射精管平滑肌及上皮下区域的神经纤维。供应生殖组织的血管外膜内的内皮细胞和神经丛也呈NOS阳性。NOS的其他定位还存在于附睾和凝固腺的上皮细胞内。(摘要截短于250字)

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