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兔单条肾单位中激肽释放酶样活性的定位

Localization of kallikrein-like activity along a single nephron in rabbits.

作者信息

Tomita K, Endou H, Sakai F

出版信息

Pflugers Arch. 1981 Jan;389(2):91-5. doi: 10.1007/BF00582097.

Abstract

In order to investigate the presence of renal kallikrein, the localization of kallikrein-like proteolytic activity along a single nephron was determined in rabbits. Single nephrons were dissected into 8 segments under a microscope. Activity was fluorometrically measured with two different substrates (benzoyl-L-arginine ethyl ester: BAEE and prolyl-phenylalanyl-arginine-methylcoumarin amide: MCA). Proteolytic activity could be detected in the early (S1), the middle (S2), and the terminal (S3) portions of the proximal tubule and in the granular portion of the distal tubule (DCTg). With MCA, the specific activity in S1, S2, S3 and DCTg was 0.77 +/- 0.08, 0.28 +/- 0.10, 0.13 +/- 0.05, and 0.27 +/- 0.05 pmoles/microgram/min, respectively. The activity in DCTg was inhibited by aprotinin but that in the proximal tubules was not inhibited. No activity was found in the glomerulus, the thick ascending limb of Henle's loop, the bright portion of the distal tubule, and the light portion of the cortical collecting tubule. The inhibition of the activity by aprotinin in DCTg suggests that intrarenal kallikrein could be localized only in DCTg.

摘要

为了研究肾激肽释放酶的存在情况,在兔子身上确定了沿单个肾单位的类激肽释放酶蛋白水解活性的定位。在显微镜下将单个肾单位 dissected 成 8 个节段。用两种不同的底物(苯甲酰-L-精氨酸乙酯:BAEE 和脯氨酰-苯丙氨酰-精氨酸-甲基香豆素酰胺:MCA)通过荧光法测量活性。在近端小管的早期(S1)、中期(S2)和终末期(S3)部分以及远端小管的颗粒部分(DCTg)可检测到蛋白水解活性。使用 MCA 时,S1、S2、S3 和 DCTg 中的比活性分别为 0.77±0.08、0.28±0.10、0.13±0.05 和 0.27±0.05 皮摩尔/微克/分钟。DCTg 中的活性被抑肽酶抑制,但近端小管中的活性未被抑制。在肾小球、亨氏袢的厚升支、远端小管的明亮部分和皮质集合小管的浅色部分未发现活性。抑肽酶对 DCTg 中活性的抑制表明肾内激肽释放酶可能仅定位于 DCTg。 (注:dissected 这个词在语境中不太好准确翻译,这里暂保留英文,可能需要结合更详细背景准确理解其含义)

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