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胰岛素诱导四氧嘧啶处理的糖尿病小鼠形成肉芽肿组织并促进血管生成。

Insulin-induced granuloma tissue formation and angiogenesis in alloxan-treated diabetic mice.

作者信息

Kimura M, Amemiya K, Suzuki J

出版信息

Endocrinol Jpn. 1987 Feb;34(1):55-63. doi: 10.1507/endocrj1954.34.55.

Abstract

Pouch granuloma formation induced by Freund's complete adjuvant containing 0.1% croton oil was studied in both normal and alloxan-induced diabetic mice, and was found to be significantly suppressed in the diabetic group. Insulin repeatedly injected into the pouch facilitated granuloma formation dose-dependently, especially in the diabetic mice. The topical insulin treatment did not affect blood glucose levels. The suppression of granuloma formation by diabetes and its reverse by insulin treatment were verified by histological findings in the granuloma pouch wall. Characteristic changes in neovascularization occurred in the pouch wall. The hydroxyproline content in the granuloma tissue in diabetic mice was not significantly enhanced by the insulin treatment. This indicates that differences in collagen production in normal and diabetic mice were not the critical factor affecting granuloma formation. It was concluded that the decreased granuloma formation in the diabetic state was due to the lack of insulin as a growth factor, and that angiogenesis induced by insulin preceding collagen fiber formation may play an essential role in granuloma formation.

摘要

在正常小鼠和四氧嘧啶诱导的糖尿病小鼠中,研究了含0.1%巴豆油的弗氏完全佐剂诱导的袋状肉芽肿形成,发现糖尿病组的肉芽肿形成受到显著抑制。反复注射到袋中的胰岛素剂量依赖性地促进肉芽肿形成,尤其是在糖尿病小鼠中。局部胰岛素治疗不影响血糖水平。通过肉芽肿袋壁的组织学发现证实了糖尿病对肉芽肿形成的抑制作用及其通过胰岛素治疗的逆转。袋壁出现了新生血管形成的特征性变化。胰岛素治疗并未显著提高糖尿病小鼠肉芽肿组织中的羟脯氨酸含量。这表明正常小鼠和糖尿病小鼠中胶原蛋白产生的差异不是影响肉芽肿形成的关键因素。得出的结论是,糖尿病状态下肉芽肿形成减少是由于缺乏作为生长因子的胰岛素,并且胰岛素在胶原纤维形成之前诱导的血管生成可能在肉芽肿形成中起重要作用。

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