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有尾两栖类动物肾脏和肾上腺组织中的心房钠尿肽(ANF)受体——这些组织中缺乏血管紧张素II(A II)受体。

Receptors for atrial natriuretic factor (ANF) in kidney and adrenal tissue of urodeles--lack of angiotensin II (A II) receptors in these tissues.

作者信息

Kloas W, Hanke W

机构信息

Department of Zoology II, University of Karlsruhe, Federal Republic of Germany.

出版信息

Gen Comp Endocrinol. 1993 Sep;91(3):235-49. doi: 10.1006/gcen.1993.1123.

Abstract

Binding sites for atrial natriuretic factor (ANF) and angiotensin II (A II) were localized and quantified in renal and adrenal tissue of the Urodele Ambystoma mexicanum by quantitative in vitro autoradiography using 125I-ratANF(99-126) and 125I-[Val5]-A II or 125I-human A II as labeled ligands. Specific 125I-ratANF(99-126) binding was present in glomeruli, renal tubules, and adrenal tissue. ANF had heterogeneous binding sites exhibiting positive cooperativity with a half maximal binding concentration (EC50) of 124 +/- 12 pM in glomeruli and 118 +/- 18 pM in adrenal tissue (n = 8). The corresponding maximal binding capacities (Bmax) were 0.84 +/- 0.10 and 0.72 +/- 0.18 femtomol/mm2. 125I-ratANF(99-126) binding was competitively displaced by unlabeled ANF analogues with an intact disulfide bridge showing a lower affinity than the iodinated ligand. In in vitro perifusion experiments ANF inhibited basal as well as ACTH-stimulated steroid secretion whereas catecholamine release was not affected indicating that ANF binding in adrenal tissue is restricted to steroidogenic interrenal cells. In vivo experiments demonstrated that during acclimation to 1.5% salt water made using seawater salt the number of ANF binding sites in kidney glomeruli decreased after 12 hr and 7 days while no significant changes were observed in adrenal tissue. No A II binding sites were detected either in renal or adrenal tissue indicating a lack of A II receptors in these tissues, which was confirmed by in vitro perifusion experiments which showed that A II did not affect adrenal steroid and catecholamine secretion.

摘要

利用¹²⁵I - 大鼠心房钠尿肽(99 - 126)和¹²⁵I - [缬氨酸⁵] - 血管紧张素II或¹²⁵I - 人血管紧张素II作为标记配体,通过定量体外放射自显影技术,在有尾两栖动物墨西哥钝口螈的肾脏和肾上腺组织中对心房钠尿肽(ANF)和血管紧张素II(A II)的结合位点进行了定位和定量分析。肾小球、肾小管和肾上腺组织中存在特异性的¹²⁵I - 大鼠心房钠尿肽(99 - 126)结合。心房钠尿肽具有异质性结合位点,表现出正协同性,在肾小球中的半数最大结合浓度(EC50)为124±12 pM,在肾上腺组织中为118±18 pM(n = 8)。相应的最大结合容量(Bmax)分别为0.84±0.10和0.72±0.18飞摩尔/平方毫米。¹²⁵I - 大鼠心房钠尿肽(99 - 126)的结合可被具有完整二硫键的未标记心房钠尿肽类似物竞争性取代,这些类似物的亲和力低于碘化配体。在体外灌流实验中,心房钠尿肽抑制基础以及促肾上腺皮质激素刺激的类固醇分泌,而儿茶酚胺释放不受影响,这表明肾上腺组织中的心房钠尿肽结合仅限于类固醇生成的肾间细胞。体内实验表明,在适应使用海水盐配制的1.5%盐水的过程中,肾小球中ANF结合位点的数量在12小时和7天后减少,而肾上腺组织中未观察到显著变化。在肾脏或肾上腺组织中均未检测到A II结合位点,这表明这些组织中缺乏A II受体,体外灌流实验证实A II不影响肾上腺类固醇和儿茶酚胺的分泌。

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