Substance P antagonists: meet the new drugs, same as the old drugs? Insights from transgenic animal models.
CNS Spectr
; 8(8): 589-96, 2003 Aug.
Article
em En
| MEDLINE
| ID: mdl-12907922
Antidepressants that primarily target the reuptake of monoamines have been highly successful treatments. However, therapies with these drugs still have several drawbacks, namely severe side effects, delays in the onset of action, and a significant percentage of non-responders. Recently, non-peptidic antagonists of the neurokinin 1 receptor, or substance P antagonists, have emerged as a novel class of drugs with antidepressant efficacy that is comparable to current drugs, but a potentially reduced side effect profile. This review summarizes the pre-clinical evidence derived from pharmacological and transgenic animal studies that suggests an important role for the substance P/neurokinin 1 system in anxiety and depression. Also, potential mechanisms by which substance P antagonists may produce their therapeutic effects are discussed.
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Base de dados:
MEDLINE
Assunto principal:
Transtornos de Ansiedade
/
Ansiolíticos
/
Substância P
/
Drogas em Investigação
/
Receptores da Neurocinina-1
/
Transtorno Depressivo
/
Antidepressivos
Limite:
Animals
/
Humans
Idioma:
En
Revista:
CNS Spectr
Assunto da revista:
NEUROLOGIA
Ano de publicação:
2003
Tipo de documento:
Article
País de afiliação:
Estados Unidos