Analgesic and side effects of intravenous recombinant Phα1β

Author:

Rigo Flavia Karine1,Rossato Mateus Fortes2,Borges Vanessa2,Silva Juliana Figueira da3,Pereira Elizete Maria Rita3,Ávila Ricardo Andrez Machado de1,Trevisan Gabriela1,Santos Duana Carvalho dos3,Diniz Danuza Montijo3,Silva Marco Aurélio Romano4ORCID,Castro Junior Célio José de3,Cunha Thiago Mattar2,Ferreira Juliano5,Gomez Marcus Vinicius3ORCID

Affiliation:

1. University of the Extreme South of Santa Catarina (UNESC), Brazil

2. University of São Paulo (USP), Brazil

3. Santa Casa of Belo Horizonte Group, Brazil

4. Federal University of Minas Gerais (UFMG), Brazil

5. Federal University of Santa Catarina, Brazil

Publisher

FapUNIFESP (SciELO)

Subject

Infectious Diseases,Toxicology,Animal Science and Zoology,Parasitology

Reference44 articles.

1. Polypeptide ω‐conotoxin GVIA as a basis for new analgesic and neuroprotective agents;Norton RS;Drug Dev Res,1999

2. Targeting Ca2+ channels to treat pain: T-type versus N-type;Altier C;Trends Pharmacol Sci,2004

3. Selective N-type neuronal voltage-sensitive calcium channel blocker, SNX-111, produces spinal antinociception in rat models of acute, persistent and neuropathic pain;Bowersox SS;J Pharmacol Exp Ther,1996

4. Antagonists of neuronal calcium channels: structure, function, and therapeutic implications;Miljanich GP;Annu Rev Pharmacol Toxicol,1995

5. Ziconotide: neuronal calcium channel blocker for treating severe chronic pain;Miljanich GP;Curr Med Chem,2004

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