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长期服用卡马西平可选择性下调大鼠脑中胞质型磷脂酶A2的表达及环氧化酶活性。

Chronic carbamazepine selectively downregulates cytosolic phospholipase A2 expression and cyclooxygenase activity in rat brain.

作者信息

Ghelardoni Sandra, Tomita York A, Bell Jane M, Rapoport Stanley I, Bosetti Francesca

机构信息

Brain Physiology and Metabolism Section, National Institute on Aging, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Biol Psychiatry. 2004 Aug 15;56(4):248-54. doi: 10.1016/j.biopsych.2004.05.012.

Abstract

BACKGROUND

Carbamazepine is a mood stabilizer used as monotherapy or as an adjunct to lithium in the treatment of acute mania or the prophylaxis of bipolar disorder. Based on evidence that lithium and valproate, other mood stabilizers, reduce brain arachidonic acid turnover and its conversion via cyclooxygenase to prostaglandin E(2) in rat brain, one possibility is that carbamazepine also targets the arachidonic acid cascade.

METHODS

To test this hypothesis, carbamazepine was administered to rats by intraperitoneal injection at a daily dose of 25 mg/kg for 30 days.

RESULTS

Carbamazepine decreased brain phospholipase A(2) activity and cytosolic phospholipase A(2) protein and messenger RNA levels without changing significantly protein and activity levels of calcium-independent phospholipase A(2) or secretory phospholipase A(2). Cyclooxygenase activity was decreased in carbamazepine-treated rats without any change in cyclooxygenase-1 or cyclooxygenase-2 protein levels. Brain prostaglandin E(2) concentration also was reduced. The protein levels of other arachidonic acid metabolizing enzymes, 5-lipoxygenase and cytochrome P450 epoxygenase, were not significantly changed nor was the brain concentration of the 5-lipoxygenase product leukotriene B(4).

CONCLUSIONS

Carbamazepine downregulates cytosolic phospholipase A(2)-mediated release of arachidonic acid and its subsequent conversion to prostaglandin E(2) by cyclooxygenase. These effects may contribute to its therapeutic actions in bipolar disorder.

摘要

背景

卡马西平是一种心境稳定剂,可作为单一疗法或作为锂盐的辅助药物用于治疗急性躁狂症或预防双相情感障碍。基于锂盐和丙戊酸盐(其他心境稳定剂)可降低大鼠脑内花生四烯酸周转率及其通过环氧化酶转化为前列腺素E2的证据,一种可能性是卡马西平也作用于花生四烯酸级联反应。

方法

为验证这一假设,给大鼠腹腔注射卡马西平,每日剂量为25mg/kg,持续30天。

结果

卡马西平降低了脑磷脂酶A2活性、胞质型磷脂酶A2蛋白及信使核糖核酸水平,而不依赖钙的磷脂酶A2或分泌型磷脂酶A2的蛋白及活性水平无明显变化。卡马西平治疗的大鼠环氧化酶活性降低,而环氧化酶-1或环氧化酶-2蛋白水平无任何改变。脑内前列腺素E2浓度也降低。其他花生四烯酸代谢酶5-脂氧合酶和细胞色素P450环氧合酶的蛋白水平无明显变化,5-脂氧合酶产物白三烯B4的脑内浓度也无明显变化。

结论

卡马西平下调胞质型磷脂酶A2介导的花生四烯酸释放及其随后通过环氧化酶转化为前列腺素E2的过程。这些作用可能有助于其在双相情感障碍中的治疗作用。

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