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Verapamil concentrations in cerebrospinal fluid after oral administration.

作者信息

Doran A R, Narang P K, Meigs C Y, Wolkowitz O M, Roy A, Breier A, Pickar D

出版信息

N Engl J Med. 1985 May 9;312(19):1261-2.

PMID:3990723
Abstract
摘要

相似文献

1
Verapamil concentrations in cerebrospinal fluid after oral administration.口服给药后脑脊液中的维拉帕米浓度。
N Engl J Med. 1985 May 9;312(19):1261-2.
2
Steady-state cerebrospinal fluid transfer of verapamil and metabolites in patients with schizophrenia.精神分裂症患者中维拉帕米及其代谢产物的稳态脑脊液转运
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3
[Pharmacokinetics and pharmacodynamics of verapamil in healthy volunteers after single oral and sublingual administration].[单次口服和舌下给药后维拉帕米在健康志愿者体内的药代动力学和药效学]
Arzneimittelforschung. 1982;32(12):1567-71.
4
Faster clearance of sustained release verapamil in men versus women: continuing observations on sex-specific differences after oral administration of verapamil.男性对缓释维拉帕米的清除速度快于女性:口服维拉帕米后性别差异的持续观察。
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5
Plasma concentrations of S-verapamil after single doses of two different galenic formulations of racemic verapamil.消旋维拉帕米两种不同剂型单剂量给药后S-维拉帕米的血浆浓度。
Arzneimittelforschung. 1993 May;43(5):520-2.
6
Differential induction of prehepatic and hepatic metabolism of verapamil by rifampin.利福平对维拉帕米肝前代谢和肝脏代谢的差异诱导作用。
Hepatology. 1996 Oct;24(4):796-801. doi: 10.1002/hep.510240407.
7
PQ-intervals and serum concentrations as indices of verapamil absorption following sublingual, buccal and per oral administration in man.在人体中,舌下、颊部及口服维拉帕米后,以PQ间期和血清浓度作为维拉帕米吸收的指标。
Methods Find Exp Clin Pharmacol. 1983 Oct;5(8):537-41.
8
Unexpected effect of verapamil on oral bioavailability of the beta-blocker talinolol in humans.维拉帕米对β受体阻滞剂他林洛尔人体口服生物利用度的意外影响。
Clin Pharmacol Ther. 1999 Mar;65(3):283-90. doi: 10.1016/S0009-9236(99)70107-4.
9
Verapamil disposition and effect on PQ-intervals after buccal, oral and intravenous administration.维拉帕米经颊、口服和静脉给药后的处置及其对PQ间期的影响。
Arzneimittelforschung. 1984;34(4):498-502.
10
Verapamil stereoisomerism: enantiomeric ratios in plasma dependent on peak concentrations, oral input rate, or both.
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A systematic review of calcium channel antagonists in bipolar disorder and some considerations for their future development.双相情感障碍中钙通道拮抗剂的系统评价及其未来发展的若干思考
Mol Psychiatry. 2016 Oct;21(10):1324-32. doi: 10.1038/mp.2016.86. Epub 2016 May 31.
2
Dopaminergic function in rat brain after oral administration of calcium-channel blockers or haloperidol. A microdialysis study.
J Neural Transm Gen Sect. 1994;95(3):195-207. doi: 10.1007/BF01271566.
3
Time-course of changes in water, sodium, potassium and calcium contents of various brain regions in rats after systemic kainic acid administration.
Acta Neuropathol. 1986;70(2):169-76. doi: 10.1007/BF00691435.
4
Anticonvulsant effects of some calcium entry blockers in DBA/2 mice.某些钙通道阻滞剂对DBA/2小鼠的抗惊厥作用。
Br J Pharmacol. 1988 Feb;93(2):247-56. doi: 10.1111/j.1476-5381.1988.tb11428.x.
5
Verapamil. An updated review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in hypertension.维拉帕米。对其药效学和药代动力学特性以及在高血压治疗中的应用的最新综述。
Drugs. 1989 Jul;38(1):19-76. doi: 10.2165/00003495-198938010-00003.
6
Do calcium antagonists have a place in the treatment of mood disorders?钙拮抗剂在情绪障碍的治疗中有一席之地吗?
Drugs. 1991 Nov;42(5):721-9. doi: 10.2165/00003495-199142050-00001.
7
Psychopharmacological properties of calcium channel inhibitors.钙通道抑制剂的精神药理学特性。
Psychopharmacology (Berl). 1992;109(1-2):12-29. doi: 10.1007/BF02245476.