• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

马拉硫磷处理的高血糖动物的脑糖原分解和糖酵解

Cerebral glycogenolysis and glycolysis in malathion-treated hyperglycaemic animals.

作者信息

Matin M A, Husain K

出版信息

Biochem Pharmacol. 1987 Jun 1;36(11):1815-7. doi: 10.1016/0006-2952(87)90243-7.

DOI:10.1016/0006-2952(87)90243-7
PMID:3579975
Abstract

Treatment with malathion resulted in an increase in the level of blood glucose and lactate and reduced cerebral glycogen, 2 hr after its administration. The blood pyruvate level was not changed. The activities of glycogenolytic enzymes (glycogen phosphorylase and phosphoglucomutase) were increased significantly in the brain, whereas that of glucose-6-phosphatase remained unchanged. The activity of the glycolytic enzyme-hexokinase was increased significantly in malathion-treated animals, whereas those of the glucose-6-phosphate and lactate dehydrogenases were not significantly changed. The changes in enzyme activities may be a compensatory mechanism to provide energy in the form of glucose to cerebral tissue on account of stimulatory effects in malathion-treated animals.

摘要

马拉硫磷给药2小时后,治疗导致血糖和乳酸水平升高,脑糖原减少。血丙酮酸水平未改变。脑内糖原分解酶(糖原磷酸化酶和磷酸葡萄糖变位酶)的活性显著增加,而葡萄糖-6-磷酸酶的活性保持不变。在接受马拉硫磷治疗的动物中,糖酵解酶己糖激酶的活性显著增加,而葡萄糖-6-磷酸脱氢酶和乳酸脱氢酶的活性没有显著变化。酶活性的变化可能是一种补偿机制,由于马拉硫磷对动物的刺激作用,以葡萄糖的形式为脑组织提供能量。

相似文献

1
Cerebral glycogenolysis and glycolysis in malathion-treated hyperglycaemic animals.马拉硫磷处理的高血糖动物的脑糖原分解和糖酵解
Biochem Pharmacol. 1987 Jun 1;36(11):1815-7. doi: 10.1016/0006-2952(87)90243-7.
2
Changes in cerebral glycogenolysis and related enzymes in diazinon treated hyperglycaemic animals.
J Appl Toxicol. 1987 Apr;7(2):131-4. doi: 10.1002/jat.2550070210.
3
Modification of malathion induced neurochemical changes by adrenalectomy in rats.肾上腺切除术对大鼠马拉硫磷诱导的神经化学变化的影响
Mol Chem Neuropathol. 1990 Aug-Oct;13(1-2):119-28. doi: 10.1007/BF03159913.
4
Modification of diazinon-induced changes in carbohydrate metabolism by adrenalectomy in rats.
Biochem Pharmacol. 1990 Jun 1;39(11):1781-6. doi: 10.1016/0006-2952(90)90125-5.
5
The role of adrenals in diazinon-induced changes in carbohydrate metabolism in rats.肾上腺在二嗪农诱导的大鼠碳水化合物代谢变化中的作用。
Arh Hig Rada Toksikol. 1990 Dec;41(4):347-56.
6
Influence of cholinergic and adrenergic blocking drugs on hyperglycemia and brain glycogenolysis in diazinon-treated animals.胆碱能和肾上腺素能阻断药物对经二嗪农处理动物的高血糖和脑糖原分解的影响。
Can J Physiol Pharmacol. 1988 Sep;66(9):1144-7. doi: 10.1139/y88-188.
7
Effect of subchronic exposure to malathion on glycogen phosphorylase and hexokinase activities in rat liver using native PAGE.使用非变性聚丙烯酰胺凝胶电泳法研究大鼠肝脏亚慢性马拉硫磷暴露对糖原磷酸化酶和己糖激酶活性的影响。
Toxicology. 2006 Jun 1;223(1-2):9-14. doi: 10.1016/j.tox.2006.02.020. Epub 2006 Apr 18.
8
Effect of adrenalectomy on diazinon-induced changes in carbohydrate metabolism.肾上腺切除术对二嗪农诱导的碳水化合物代谢变化的影响。
Arch Toxicol. 1989;63(5):376-80. doi: 10.1007/BF00303126.
9
Cerebral glucose and glycogen metabolism in diazinon-treated animals.
J Biochem Toxicol. 1987 Fall-Winter;2:265-70. doi: 10.1002/jbt.2570020310.
10
Actions of glucagon on flux rates in perfused rat liver. 1. Kinetics of the inhibitory effect on glycolysis and the stimulatory effect on glycogenolysis.胰高血糖素对灌注大鼠肝脏通量率的作用。1. 对糖酵解的抑制作用和对糖原分解的刺激作用的动力学。
Eur J Biochem. 1983 Nov 15;136(3):609-16. doi: 10.1111/j.1432-1033.1983.tb07784.x.

引用本文的文献

1
Effects of Pesticides on Longevity and Bioenergetics in Invertebrates-The Impact of Polyphenolic Metabolites.农药对无脊椎动物寿命和生物能量学的影响-多酚代谢物的影响。
Int J Mol Sci. 2021 Dec 15;22(24):13478. doi: 10.3390/ijms222413478.
2
Potential contribution of insecticide exposure and development of obesity and type 2 diabetes.杀虫剂暴露与肥胖症和2型糖尿病发生发展之间的潜在关联。
Food Chem Toxicol. 2017 Jul;105:456-474. doi: 10.1016/j.fct.2017.05.003. Epub 2017 May 6.