Site 1 sodium channel blockers prolong the duration of sciatic nerve blockade from tricyclic antidepressants

被引:24
作者
Barnet, CS
Tse, JY
Kohane, DS
机构
[1] Massachusetts Gen Hosp, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Pediat Intens Care Unit, Boston, MA 02114 USA
[3] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
关键词
sodium channel blockers; nerve blockade; bupivacaine; tricyclic antidepressants; local anesthetics; tetrodotoxin;
D O I
10.1016/j.pain.2004.04.027
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Many recent reports in the literature address the local anesthetics efficacy of tricyclic antidepressants (TCAs). Here we investigated whether nerve block from TCAs is prolonged by site 1 sodium channel blockers such as tetrodotoxin and saxitoxin, which are known to prolong block from conventional local anesthetics. Tetrodotoxin and saxitoxin greatly prolonged block from TCAs. For example, the median duration of thermal nociceptive blocks for 10 mM amitriptyline, nortriptyline and doxepin were 0, 0, and 124 min; co-injection with 20 muM TTX (median block duration = 0), yielded blocks lasting 404, 325, and 697 min, respectively. Co-injection of 12 muM saxitoxin (median block duration= 0) with 10 mM amitriptyline resulted in a thermal nociceptive block duration of 373 min. Co-injection of 7.7 mM bupivacaine and 7.7 mM amiptriptyline did not result in block prolongation. Systemic (subcutaneous) delivery of tetrodotoxin or amitriptyline did not result in prolongation of block from the other class of drug injected at the sciatic nerve. In TCA-containing formulations, motor blockade was consistently longer than thermal nociceptive block; motor blockade was also prolonged by tetrodotoxin and saxitoxin. In summary site 1 sodium channel blockers prolong the duration of TCAs via a locally mediated mechanism. (C) 2004 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:432 / 438
页数:7
相关论文
共 23 条
[1]  
ADAMS HJ, 1976, ANESTH ANALG, V55, P568
[2]  
ADAMS HJ, 1976, ARCH INT PHARMACOD T, V224, P275
[3]   PHARMACOLOGIC CORRELATION BETWEEN LOCAL ANESTHETIC-INDUCED MYOTOXICITY AND DISTURBANCES OF INTRACELLULAR CALCIUM DISTRIBUTION [J].
BENOIT, PW ;
YAGIELA, JA ;
FORT, NF .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1980, 52 (02) :187-198
[4]   PHYSICAL AND CHEMICAL-PROPERTIES OF DRUG MOLECULES GOVERNING THEIR DIFFUSION THROUGH THE SPINAL MENINGES [J].
BERNARDS, CM ;
HILL, HF .
ANESTHESIOLOGY, 1992, 77 (04) :750-756
[5]   Amitriptyline - A review of its pharmacological properties and therapeutic use in chronic pain states [J].
Bryson, HM ;
Wilde, MI .
DRUGS & AGING, 1996, 8 (06) :459-476
[7]   Assessment of differential blockade by amitriptyline and its N-methyl derivative in different species by different routes [J].
Gerner, P ;
Haderer, AE ;
Mujtaba, M ;
Sudoh, Y ;
Narang, S ;
Abdi, S ;
Srinivasa, V ;
Pertl, C ;
Wang, GK .
ANESTHESIOLOGY, 2003, 98 (06) :1484-1490
[8]   Amitriptyline versus bupivacaine in rat sciatic nerve blockade [J].
Gerner, P ;
Mujtaba, M ;
Sinnott, CJ ;
Wang, GK .
ANESTHESIOLOGY, 2001, 94 (04) :661-667
[9]  
KAO CY, 1972, FED PROC, V31, P1117
[10]  
KAO CY, 1966, PHARMACOL REV, V18, P997