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母鸡对¹²⁵I标记胰岛素的肾脏处理

Renal handling of 125I-labelled insulin in the hen.

作者信息

Milton A, Odlind B, Wibell L, Dencker L

出版信息

Diabetes Res. 1985 May;2(3):163-9.

PMID:2998679
Abstract

Renal handling of 125I-insulin was studied using a modification of the Sperber technique. Results showed 125I-insulin to be extracted at the peritubular side of the nephron in a process that was competitively inhibited by increasing amounts of unlabelled insulin, but not ACTH, in the injection mixture. When unlabelled insulin instead was injected 30 sec after the labelled insulin it showed significantly less interference with peritubular extraction of 125I-insulin, indicating strong attachment to the cell membrane or possible internalization of 125I-insulin into proximal tubular cells. Light microscope autoradiography 1 min after injection of 125I-insulin showed grains over proximal tubules only. On the ligated side localization was preferably peritubular while on the control side it was luminal. Electron microscope autoradiography showed sparsely distributed grains, however, frequently located over basal parts of proximal tubular cells. Pretreatment with lysine hydrochloride lowered renal extraction of 125I-insulin and increased urinary recovery of iodine label bilaterally. 125I-glucagon and 125I-C-peptide were not extracted from the peritubular circulation. In conclusion, the model has provided evidence of a rapid and significant peritubular extraction of 125I-insulin by proximal tubular cells in a process probably involving specific insulin receptors. Following receptor binding probably only minor amounts of 125I-insulin enters the proximal tubular cells, while the greater part is degraded at the cell surface or released into the circulation.

摘要

采用改良的斯珀伯技术研究了肾脏对¹²⁵I胰岛素的处理。结果显示,¹²⁵I胰岛素在肾单位的肾小管周围侧被提取,该过程受到注射混合物中未标记胰岛素量增加的竞争性抑制,但不受促肾上腺皮质激素(ACTH)的抑制。当在标记胰岛素注射30秒后注射未标记胰岛素时,其对¹²⁵I胰岛素肾小管周围提取的干扰明显减少,这表明¹²⁵I胰岛素与细胞膜有强附着或可能内化进入近端肾小管细胞。注射¹²⁵I胰岛素1分钟后的光学显微镜放射自显影显示仅在近端小管上有银粒。在结扎侧,定位主要在肾小管周围,而在对照侧则在管腔内。电子显微镜放射自显影显示银粒分布稀疏,但经常位于近端肾小管细胞的基部。用盐酸赖氨酸预处理可降低¹²⁵I胰岛素的肾脏提取率,并双侧增加碘标记物的尿回收率。¹²⁵I胰高血糖素和¹²⁵I C肽未从肾小管周围循环中被提取。总之,该模型提供了证据,表明近端肾小管细胞对¹²⁵I胰岛素有快速且显著的肾小管周围提取,这一过程可能涉及特定的胰岛素受体。受体结合后,可能只有少量的¹²⁵I胰岛素进入近端肾小管细胞,而大部分在细胞表面降解或释放到循环中。

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