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胰岛素、糖皮质激素和甲状腺激素对大鼠巨噬细胞中糖酵解、谷氨酰胺分解、磷酸戊糖途径和三羧酸循环关键酶活性的影响。

Effects of insulin, glucocorticoids and thyroid hormones on the activities of key enzymes of glycolysis, glutaminolysis, the pentose-phosphate pathway and the Krebs cycle in rat macrophages.

作者信息

Rosa L F, Cury Y, Curi R

机构信息

Laboratory of Pathophysiology, Instituto Butantan, São Paulo, Brazil.

出版信息

J Endocrinol. 1992 Nov;135(2):213-9. doi: 10.1677/joe.0.1350213.

Abstract

In the present study the effects of insulin, glucocorticoids and thyroid hormones on macrophage metabolism and function were investigated. The maximum activities of hexokinase, glucose-6-phosphate dehydrogenase, glutaminase and citrate synthase were determined in macrophages obtained from hormone-treated rats and those cultured for a period of 48 h in the presence of hormones. Macrophage phagocytosis was markedly inhibited by dexamethasone and thyroid hormones, remaining unchanged when insulin was added to the culture medium, however. The changes in the enzyme activities caused by hormone treatments of the rats were very similar to those found in culture. Insulin enhanced citrate synthase and hexokinase activities and diminished those of glutaminase and glucose-6-phosphate dehydrogenase. Dexamethasone had a similar effect except on glucose-6-phosphate dehydrogenase. The addition of thyroid hormones to the culture medium raised the activities of glutaminase and hexokinase and reduced that of citrate synthase. The results presented support the suggestion that the effects of insulin, glucocorticoids and thyroid hormones on immune and inflammatory responses could well be mediated through changes in macrophage metabolism.

摘要

在本研究中,研究了胰岛素、糖皮质激素和甲状腺激素对巨噬细胞代谢和功能的影响。测定了从激素处理大鼠获得的巨噬细胞以及在激素存在下培养48小时的巨噬细胞中己糖激酶、葡萄糖-6-磷酸脱氢酶、谷氨酰胺酶和柠檬酸合酶的最大活性。地塞米松和甲状腺激素显著抑制巨噬细胞吞噬作用,然而,当向培养基中添加胰岛素时,巨噬细胞吞噬作用保持不变。对大鼠进行激素处理引起的酶活性变化与在培养中发现的变化非常相似。胰岛素增强了柠檬酸合酶和己糖激酶的活性,并降低了谷氨酰胺酶和葡萄糖-6-磷酸脱氢酶的活性。地塞米松有类似的作用,但对葡萄糖-6-磷酸脱氢酶除外。向培养基中添加甲状腺激素提高了谷氨酰胺酶和己糖激酶的活性,并降低了柠檬酸合酶的活性。所呈现的结果支持这样的观点,即胰岛素、糖皮质激素和甲状腺激素对免疫和炎症反应的影响很可能是通过巨噬细胞代谢的变化介导的。

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