Clinical uses of α2-adrenergic agonists

被引：689

作者：

Kamibayashi, T

Maze, M

机构：

[1] Chelsea & Westminster Hosp, Magill Dept Anaesthet, Imperial Coll, Sch Med, London SW10 9NH, England

[2] Osaka Univ, Dept Anesthesia & Acute Crit Med, Grad Sch Med, Osaka, Japan

来源：

ANESTHESIOLOGY | 2000年 / 93卷 / 05期

关键词：

alpha(2)-adrenergic receptor; anesthesia; anxiolysis; clonidine; dexmedetomidine; pain; sedation; sympatholysis;

D O I：

10.1097/00000542-200011000-00030

中图分类号：

R614 [麻醉学];

学科分类号：

100217 ;

摘要：

[No abstract available]

引用

页码：1345 / 1349

页数：5

共 20 条

[1]

Bachand Romeo T., 1999, Anesthesiology (Hagerstown), V91, pA296

[2] The effects of increasing plasma concentrations of dexmedetomidine in humans [J].

Ebert, TJ ;

Hall, JE ;

Barney, JA ;

Uhrich, TD ;

Colinco, MD .

ANESTHESIOLOGY, 2000, 93 (02) :382-394

[3] Intrathecal, but not intravenous, clonidine reduces experimental thermal or capsaicin-induced pain and hyperalgesia in normal volunteers [J].

Eisenach, JC ;

Hood, DD ;

Curry, R .

ANESTHESIA AND ANALGESIA, 1998, 87 (03) :591-596

[4] alpha(2)-adrenergic agonists for regional anesthesia - A clinical review of clonidine (1984-1995) [J].

Eisenach, JC ;

DeKock, M ;

Klimscha, W .

ANESTHESIOLOGY, 1996, 85 (03) :655-674

[5] The α-2a noradrenergic agonist, guanfacine, improves delayed response performance in young adult rhesus monkeys [J].

Franowicz, JS ;

Arnsten, AFT .

PSYCHOPHARMACOLOGY, 1998, 136 (01) :8-14

[6] Intrathecal clonidine combined with sufentanil for labor analgesia [J].

Gautier, PE ;

De Kock, M ;

Fanard, L ;

Van Steenberge, A ;

Hody, JL .

ANESTHESIOLOGY, 1998, 88 (03) :651-656

[7] Sedative, amnestic, and analgesic properties of small-dose dexmedetomidine infusions [J].

Hall, JE ;

Uhrich, TD ;

Barney, JA ;

Arain, SR ;

Ebert, TJ .

ANESTHESIA AND ANALGESIA, 2000, 90 (03) :699-705

[8] Physostigmine prevents postanesthetic shivering as does meperidine or clonidine [J].

Horn, EP ;

Standl, T ;

Sessler, DI ;

von Knobelsdorff, G ;

Büchs, C ;

Esch, JSA .

ANESTHESIOLOGY, 1998, 88 (01) :108-113

[9] Clonidine potentiates the neuropathic pain-relieving action of MK-801 while preventing its neurotoxic and hyperactivity side effects [J].

Jevtovic-Todorovic, V ;

Wozniak, DF ;

Powell, S ;

Nardi, A ;

Olney, JW .

BRAIN RESEARCH, 1998, 781 (1-2) :202-211

[10] Substitution of a mutant alpha(2a)-adrenergic receptor via ''hit and run'' gene targeting reveals the role of this subtype in sedative, analgesic, and anesthetic-sparing responses in vivo [J].

Lakhlani, PP ;

MacMillan, LB ;

Guo, TZ ;

McCool, BA ;

Lovinger, DM ;

Maze, M ;

Limbird, LE .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (18) :9950-9955

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