Butlen D, Morel F
Pflugers Arch. 1985 Aug;404(4):348-53. doi: 10.1007/BF00585347.
Binding of [125I]glucagon was measured in microdissected pieces of tubules from the rat nephron. Specific glucagon binding sites were found only in nephron segments containing a glucagon-sensitive adenylate cyclase activity. At 7.5 nM labelled hormone, higher levels of specific binding (16-27 X 10(-18) mol mm-1) were found in the thick ascending limb of the Henle's loop and in the distal convoluted tubule and lower binding levels (2-5 X 10(-18) mol mm-1) in the collecting tubule whereas specific binding could not be detected in the proximal tubule and in the thin segments of the Henle's loop. In the medullary thick ascending limb, Scatchard analysis of specific [125I]glucagon binding indicated an apparent equilibrium dissociation constant of 2.4 nM. The stereospecificity of binding sites in medullary thick ascending limbs and medullary collecting tubules, was assessed by competition experiments using unlabelled glucagon, enteroglucagon and unrelated hormones (vasopressin, calcitonin, parathyroid hormone and insulin); in both segments, glucagon was more active than enteroglucagon in displacing labelled glucagon from its tubular binding sites, whereas all other hormones tested were inactive. These results indicate that tubule binding sites might be the physiological receptors for glucagon involved in adenylate cyclase activation.
在大鼠肾单位微切割的肾小管片段中测定了[125I]胰高血糖素的结合情况。仅在含有对胰高血糖素敏感的腺苷酸环化酶活性的肾单位节段中发现了特异性胰高血糖素结合位点。在7.5 nM标记激素时,在亨氏袢的厚升支和远曲小管中发现了较高水平的特异性结合(16 - 27×10(-18) mol·mm-1),而在集合管中结合水平较低(2 - 5×10(-18) mol·mm-1),而在近端小管和亨氏袢的细段中未检测到特异性结合。在髓质厚升支中,对特异性[125I]胰高血糖素结合进行的Scatchard分析表明,表观平衡解离常数为2.4 nM。通过使用未标记的胰高血糖素、肠胰高血糖素和无关激素(血管加压素、降钙素、甲状旁腺激素和胰岛素)进行竞争实验,评估了髓质厚升支和髓质集合管中结合位点的立体特异性;在这两个节段中,胰高血糖素在从其肾小管结合位点置换标记的胰高血糖素方面比肠胰高血糖素更具活性,而所有其他测试激素均无活性。这些结果表明,肾小管结合位点可能是参与腺苷酸环化酶激活的胰高血糖素的生理受体。