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灌注大鼠附睾尾的吸收和分泌功能。

Absorptive and secretory functions of the perfused rat cauda epididymidis.

作者信息

Wong P Y, Yeung C H

出版信息

J Physiol. 1978 Feb;275:13-26. doi: 10.1113/jphysiol.1978.sp012174.

Abstract
  1. A microperfusion technique has been developed to study transport processes in the rat cauda epididymidis in vivo. 2. Na+ and water were found to be reabsorbed by the perfused rat cauda epididymidis at the rates of 3.000 +/- 0.25 n-equiv cm-1 min-1 (mean +/- S.E., n = 14) and 20.7 +/- 1.7 nl. cm-1 min-1 (mean +/- S.E., n = 14) respectively. Reabsorption of Na+ was isotonic. 3. K+ was found to be secreted into the ductal lumen at the rate of 0.124 +/- 0.016 n-equiv cm-1 min-1 (mean +/- S.E., n = 14). 4. Na+ reabsorption and water reabsorption were abolished by removing Na+ ions from the perfusion medium. The dependence of rate of net Na+ reabsorption on the intraluminal Na+ ion concentration showed saturation kinetics, with the apparent Km values of about 20 mM Na+. The dependence of water reabsorption on the intraluminal Na+ ion concentration also followed closely that of Na+. 5. Application of amiloride 10(-4) M) to the perfusion fluid abolished both Na+ and water reabsorption by the rat cauda epididymidis. 6. Removal of chloride from the perfusion fluid had no effect on Na+ and water reabsorption but increased the K+ secretion rate by threefold. 7. Proteins were also found to be secreted by the rat cauda epididymidis at a rate of 11.7 +/- 1.8 ng cm-1 min-1 (mean +/- S.E., n = 11). The secretory rate was not dependent on the intraluminal Na+ ion concentration. 8. Castration in rats abolished the reabsorption of Na+ and water and secretion of K+ and proteins by the rate cauda epididymidis. These effects could be reversed by injecting testosterone propionate into castrated rats. 9. The possible role of these transport processes in sperm maturation is discussed.
摘要
  1. 已开发出一种微灌注技术来研究大鼠附睾尾部在体内的转运过程。2. 发现灌注的大鼠附睾尾部对Na⁺和水的重吸收率分别为3.000±0.25纳当量·厘米⁻¹·分钟⁻¹(平均值±标准误,n = 14)和20.7±1.7纳升·厘米⁻¹·分钟⁻¹(平均值±标准误,n = 14)。Na⁺的重吸收是等渗的。3. 发现K⁺以0.124±0.016纳当量·厘米⁻¹·分钟⁻¹的速率分泌到管腔中(平均值±标准误,n = 14)。4. 从灌注介质中去除Na⁺离子可消除Na⁺重吸收和水重吸收。净Na⁺重吸收率对管腔内Na⁺离子浓度的依赖性呈现饱和动力学,表观Km值约为20毫摩尔/升Na⁺。水重吸收对管腔内Na⁺离子浓度的依赖性也与Na⁺密切相关。5. 向灌注液中加入10⁻⁴摩尔/升的氨氯吡脒可消除大鼠附睾尾部的Na⁺和水重吸收。6. 从灌注液中去除氯离子对Na⁺和水重吸收无影响,但使K⁺分泌速率增加了三倍。7. 还发现大鼠附睾尾部以11.7±1.8纳克·厘米⁻¹·分钟⁻¹的速率分泌蛋白质(平均值±标准误,n = 11)。分泌速率不依赖于管腔内Na⁺离子浓度。8. 大鼠去势可消除附睾尾部对Na⁺和水的重吸收以及K⁺和蛋白质的分泌。通过向去势大鼠注射丙酸睾酮可逆转这些作用。9. 讨论了这些转运过程在精子成熟中的可能作用。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15d3/1282529/f902220be7f1/jphysiol00775-0034-a.jpg

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