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性休止或性活动对大鼠腹侧前列腺结构和功能的影响。

Effects of sexual rest or sexual activity on the structure and function of the ventral prostate of the rat.

作者信息

Aumüller G, Braun B E, Seitz J, Müller T, Heyns W, Krieg M

出版信息

Anat Rec. 1985 Aug;212(4):345-52. doi: 10.1002/ar.1092120404.

Abstract

Previous studies have shown that sexual activity increases the weight of the accessory sex glands significantly, while the organ weights correlate inversely with the assayable androgen receptor concentrations in the prostate of sexually active versus sexually resting rats. In an effort to determine the structural basis of this phenomenon, the ventral prostates of adult rats kept with female rats for 4-6 months (HE-rats) were compared to those kept in groups of 5 males in one cage (HO-rats) for the same period. As an estimate of the secretory function of the gland the concentration of prostatic binding protein (PBP) was determined in prostatic cytosols using a highly specific ELISA. Catecholamines were measured by means of HPLC and subsequent electrochemical detection. Morphological studies included immunocytochemistry of PBP, visualization of adrenergic nerves, stereological analysis of stromal and glandular compartments of the prostate, and electron microscopy of the epithelium. The main findings were as follows: 1) The prostates of HE-rats were 35% heavier than those of the HO-rats. 2) The content in secretion was in the same range in both HE-rats and HO-rats (1.5 and 1.44 mg PBP per 1 mg DNA). 3) Immunocytochemistry and electron microscopy demonstrated a very homogeneous secretion within the glandular lumen of HO-rats with a diminished amount of secretory material within the glandular cells. In HE-rats the glandular lumina were clearly larger in diameter and intraluminal secretion was less homogeneously stained. The height of the epithelium was increased and the individual secretory cells contained several secretory granules.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

以往的研究表明,性活动会显著增加附属性腺的重量,而在性活跃与性静止的大鼠前列腺中,器官重量与可检测到的雄激素受体浓度呈负相关。为了确定这一现象的结构基础,将与雌鼠共处4 - 6个月的成年雄鼠(HE组大鼠)的腹侧前列腺与同期在一个笼子里5只雄鼠一组饲养的雄鼠(HO组大鼠)的腹侧前列腺进行了比较。作为对腺体分泌功能的评估,使用高度特异性的酶联免疫吸附测定法(ELISA)测定前列腺细胞溶质中前列腺结合蛋白(PBP)的浓度。通过高效液相色谱法(HPLC)和随后的电化学检测来测量儿茶酚胺。形态学研究包括PBP的免疫细胞化学、肾上腺素能神经的可视化、前列腺基质和腺腔的体视学分析以及上皮的电子显微镜检查。主要发现如下:1)HE组大鼠的前列腺比HO组大鼠的重35%。2)HE组大鼠和HO组大鼠的分泌物含量处于相同范围(每1毫克DNA含1.5和1.44毫克PBP)。3)免疫细胞化学和电子显微镜检查显示,HO组大鼠腺腔内的分泌物非常均匀,腺细胞内的分泌物质减少。在HE组大鼠中,腺腔直径明显更大,腔内分泌物染色不那么均匀。上皮高度增加,单个分泌细胞含有多个分泌颗粒。(摘要截短于250字)

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