TTA-P2 Is a Potent and Selective Blocker of T-Type Calcium Channels in Rat Sensory Neurons and a Novel Antinociceptive Agent-Reference-Cited by-同舟云学术

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TTA-P2 Is a Potent and Selective Blocker of T-Type Calcium Channels in Rat Sensory Neurons and a Novel Antinociceptive Agent

Published:2011-08-05 Issue:5 Volume:80 Page:900-910
ISSN:0026-895X
Container-title:Molecular Pharmacology
language:en
Short-container-title:Mol Pharmacol

Author:

Choe WonJoo,Messinger Richard B.,Leach Emily,Eckle Veit-Simon,Obradovic Aleksandar,Salajegheh Reza,Jevtovic-Todorovic Vesna,Todorovic Slobodan M.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference51 articles.

1. Rapid onset pain induced by intravenous streptozotocin in the rat

2. Silencing of the Cav3.2 T-type calcium channel gene in sensory neurons demonstrates its major role in nociception

3. Mechanisms of Neuropathic Pain

4. Attenuated pain responses in mice lacking CaV3.2 T-type channels

5. Inhibition of T-type voltage-gated calcium channels by a new scorpion toxin

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