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脑室内注射肌醇可拮抗锂诱导的大鼠竖毛行为抑制。

Intracerebroventricular myo-inositol antagonizes lithium-induced suppression of rearing behaviour in rats.

作者信息

Kofman O, Belmaker R H

机构信息

Beer-Sheva Mental Health Center, Ben Gurion University of the Negev, Beer-Sheva, Israel.

出版信息

Brain Res. 1990 Nov 26;534(1-2):345-7. doi: 10.1016/0006-8993(90)90155-5.

DOI:10.1016/0006-8993(90)90155-5
PMID:1963564
Abstract

Several biological effects of lithium have been reversed by in vitro myo-inositol. To determine if intracerebroventricular myo-inositol would reverse behavioural effects of lithium, rats were injected with 5 meq/kg lithium chloride or sodium chloride and injected intracranially with myo-inositol (10 mg) or artificial CSF 24 h and 15 min prior to measurement of activity in an automated activity monitor. Myo-inositol alone had no significant effect on behaviour, but significantly reversed suppression of rearing activity by lithium.

摘要

体外肌醇可逆转锂的多种生物学效应。为了确定脑室内注射肌醇是否会逆转锂的行为效应,给大鼠注射5 毫当量/千克氯化锂或氯化钠,并在通过自动活动监测仪测量活动前24小时和15分钟,向大鼠颅内注射肌醇(10毫克)或人工脑脊液。单独使用肌醇对行为没有显著影响,但能显著逆转锂对竖毛活动的抑制作用。

相似文献

1
Intracerebroventricular myo-inositol antagonizes lithium-induced suppression of rearing behaviour in rats.脑室内注射肌醇可拮抗锂诱导的大鼠竖毛行为抑制。
Brain Res. 1990 Nov 26;534(1-2):345-7. doi: 10.1016/0006-8993(90)90155-5.
2
Restoration of brain myo-inositol levels in rats increases latency to lithium-pilocarpine seizures.恢复大鼠大脑中的肌醇水平可增加锂-匹罗卡品诱导癫痫发作的潜伏期。
Psychopharmacology (Berl). 1993;110(1-2):229-34. doi: 10.1007/BF02246978.
3
Myo-inositol attenuates two specific behavioral effects of acute lithium in rats.肌醇可减轻大鼠急性锂盐的两种特定行为效应。
Psychopharmacol Bull. 1991;27(3):185-90.
4
Evidence that a proconvulsant action of lithium is mediated by inhibition of myo-inositol phosphatase in mouse brain.锂的促惊厥作用是通过抑制小鼠脑中的肌醇磷酸酶介导的证据。
Brain Res. 1991 Aug 30;558(1):145-8. doi: 10.1016/0006-8993(91)90732-b.
5
The anti-proliferative effect of lithium chloride on melanoma cells and its reversion by myo-inositol.氯化锂对黑色素瘤细胞的抗增殖作用及其被肌醇逆转的情况。
Br J Cancer. 1987 Jan;55(1):41-6. doi: 10.1038/bjc.1987.9.
6
Thyrotropin-releasing hormone reduces myo-inositol content in rat cerebellum pretreated with lithium.促甲状腺激素释放激素可降低经锂预处理的大鼠小脑肌醇含量。
J Neurochem. 1987 Jul;49(1):88-91. doi: 10.1111/j.1471-4159.1987.tb03398.x.
7
Differential uptake of lithium isotopes by rat cerebral cortex and its effect on inositol phosphate metabolism.大鼠大脑皮层对锂同位素的差异性摄取及其对磷酸肌醇代谢的影响。
J Neurochem. 1984 Mar;42(3):880-2. doi: 10.1111/j.1471-4159.1984.tb02765.x.
8
myo-Inositol reverses Li+-induced inhibition of phosphoinositide turnover and ornithine decarboxylase induction during early lymphocyte activation.肌醇可逆转锂离子在淋巴细胞早期激活过程中对磷酸肌醇转换和鸟氨酸脱羧酶诱导的抑制作用。
Eur J Immunol. 1986 Jul;16(7):859-61. doi: 10.1002/eji.1830160724.
9
Lithium-induced decrease of brain inositol and increase of brain inositol-1-phosphate is transient.锂诱导的脑内肌醇减少和脑内肌醇-1-磷酸增加是短暂的。
Neurochem Res. 1991 Aug;16(8):905-11. doi: 10.1007/BF00965540.
10
Myo-inositol attenuates the enhancement of the serotonin syndrome by lithium.肌醇可减轻锂对血清素综合征的增强作用。
Psychopharmacology (Berl). 1995 Mar;118(2):213-8. doi: 10.1007/BF02245842.

引用本文的文献

1
IP3 accumulation and/or inositol depletion: two downstream lithium's effects that may mediate its behavioral and cellular changes.肌醇三磷酸(IP3)积累和/或肌醇消耗:锂的两种下游效应,可能介导其行为和细胞变化。
Transl Psychiatry. 2016 Dec 6;6(12):e968. doi: 10.1038/tp.2016.217.
2
A safe lithium mimetic for bipolar disorder.一种用于双相情感障碍的安全锂类似物。
Nat Commun. 2013;4:1332. doi: 10.1038/ncomms2320.
3
Epi-inositol is biochemically active in reversing lithium effects on cytidine monophosphorylphosphatidate (CMP-PA). Short communication.
表肌醇在逆转锂对胞苷单磷酸磷脂酸(CMP-PA)的作用方面具有生物化学活性。简短通讯。
J Neural Transm (Vienna). 1996;103(11):1281-5. doi: 10.1007/BF01271188.
4
Restoration of brain myo-inositol levels in rats increases latency to lithium-pilocarpine seizures.恢复大鼠大脑中的肌醇水平可增加锂-匹罗卡品诱导癫痫发作的潜伏期。
Psychopharmacology (Berl). 1993;110(1-2):229-34. doi: 10.1007/BF02246978.
5
Myo-inositol attenuates the enhancement of the serotonin syndrome by lithium.肌醇可减轻锂对血清素综合征的增强作用。
Psychopharmacology (Berl). 1995 Mar;118(2):213-8. doi: 10.1007/BF02245842.