HCN1 Channels as Targets for Anesthetic and Nonanesthetic Propofol Analogs in the Amelioration of Mechanical and Thermal Hyperalgesia in a Mouse Model of Neuropathic Pain-Reference-Cited by-同舟云学术

HCN1 Channels as Targets for Anesthetic and Nonanesthetic Propofol Analogs in the Amelioration of Mechanical and Thermal Hyperalgesia in a Mouse Model of Neuropathic Pain

Published:2013-04-02 Issue:3 Volume:345 Page:363-373
ISSN:0022-3565
Container-title:Journal of Pharmacology and Experimental Therapeutics
language:en
Short-container-title:J Pharmacol Exp Ther

Author:

Tibbs Gareth R.,Rowley Thomas J.,Sanford R. Lea,Herold Karl F.,Proekt Alex,Hemmings Hugh C.,Andersen Olaf S.,Goldstein Peter A.,Flood Pamela D.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference59 articles.

1. 2,6 Di-tert-butylphenol, a Nonanesthetic Propofol Analog, Modulates α1β Glycine Receptor Function in a Manner Distinct from Propofol

2. The Non-Anaesthetic Propofol Analogue 2,6-Di-tert-Butylphenol Fails to Modulate GABA_A Receptor Function

3. Perspectives on How to Drug an Ion Channel

4. SUBHYPNOTIC DOSES OF THIOPENTONE AND PROPOFOL CAUSE ANALGESIA TO EXPERIMENTALLY INDUCED ACUTE PAIN

5. COMPARISON OF THE EFFECT OF DIISOPROPYL PHENOL (ICI 35 868) AND THIOPENTONE ON RESPONSE TO SOMATIC PAIN

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