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Ethanol inhibits the uptake of exogenous norepinephrine from the extracellular space of the rat cerebellum

Producción científica: Articlerevisión exhaustiva

28 Citas (Scopus)

Resumen

Rapid chronoamperometric recordings using nafion-coated carbon fiber electrodes coupled with pressure-ejection of drugs were used to investigate the effects of ethanol on norepinephrine (NE)-containing nerve terminals in the urethane-anesthetized Fischer 344 rat. Local application of ethanol from a double-barrel micropipette did not produce detectable changes in extracellular levels of NE in the rat cerebellar cortex. However, when ethanol was applied prior to local application of NE, it was seen to inhibit the uptake of NE from the extracellular space. These results were compared to the effects seen from the local application of a known high-affinity uptake inhibitor, nomifensine. Nomifensine was found to inhibit the extracellular uptake of NE in rat cerebeller cortex similar to ethanol. Our results support the hypothesis that one effect of ethanol on the noradrenergic system of the rat cerebellum is an alteration in the uptake of NE into NE-containing nerve endings. In addition, the present data concerning ethanol-induced inhibition of NE clearance or uptake support our previous electrophysiological studies in which we found that ethanol can potentiate the modulatory effects of β-agonists on GABA responses of cerebellar Purkinje neurons.

Idioma originalEnglish
Páginas (desde-hasta)71-75
Número de páginas5
PublicaciónNeuroscience Letters
Volumen164
N.º1-2
DOI
EstadoPublished - dic 24 1993

Nota bibliográfica

Funding Information:
The authors thank David Young for his help with statistical analysis, and special thanks to Laura Lee Lamothe for expert typing and processing of this manuscript. This work was supported by USPHS Grants AG06434, AG00441, AA05915, AA00102 and AG04418, the Veteran Administration Medical Research Services, and NSF BNS-9110308. Michael R. Palmer is supported by an ADAMHA Research Scientist Development Award. A. M.-Y. Lin is supported by an Educational Grant 27051 F from National Science Council and Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan, Republic of China.

Financiación

The authors thank David Young for his help with statistical analysis, and special thanks to Laura Lee Lamothe for expert typing and processing of this manuscript. This work was supported by USPHS Grants AG06434, AG00441, AA05915, AA00102 and AG04418, the Veteran Administration Medical Research Services, and NSF BNS-9110308. Michael R. Palmer is supported by an ADAMHA Research Scientist Development Award. A. M.-Y. Lin is supported by an Educational Grant 27051 F from National Science Council and Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan, Republic of China.

FinanciadoresNúmero del financiador
ADAMHA27051 F
Academia Sinica, Institute of Biomedical Sciences
United States Department of Veteran Administration
National Science Foundation Arctic Social Science ProgramBNS-9110308
National Institute on Alcohol Abuse and AlcoholismR01AA005915
U.S. Public Health ServiceAG00441, AG06434, AA05915, AA00102, AG04418
National Science Council
Academia Sinica, Institute of Chemistry

    ASJC Scopus subject areas

    • General Neuroscience

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