Alcohol
Volume 30, Issue 1 , Pages 9-18, May 2003

Differences in norepinephrine clearance in cerebellar slices from low-alcohol-sensitive and high-alcohol-sensitive rats

  • Ronald K Freund

      Affiliations

    • Department of Pharmacology, Box C-236, University of Colorado Health Sciences Center, 4200 East 9th Avenue, Denver, CO 80262, USA
    • Corresponding Author InformationCorresponding author. Tel.: +1-303-315-4225; fax: +1-303-315-4227
  • ,
  • Greg A Gerhardt

      Affiliations

    • Department of Anatomy and Neurobiology, University of Kentucky, Lexington, KY 40536, USA
    • Center for Sensor Technology, University of Kentucky, Lexington, KY 40536, USA
  • ,
  • Kriste E Marshall

      Affiliations

    • Department of Pharmacology, Box C-236, University of Colorado Health Sciences Center, 4200 East 9th Avenue, Denver, CO 80262, USA
  • ,
  • Michael R Palmer

      Affiliations

    • Department of Pharmacology, Box C-236, University of Colorado Health Sciences Center, 4200 East 9th Avenue, Denver, CO 80262, USA
    • Center for Sensor Technology, University of Kentucky, Lexington, KY 40536, USA

Received 31 March 2003; received in revised form 8 May 2003; accepted 11 May 2003.

Editor: T.R. Jerrells

Abstract 

High-alcohol-sensitive (HAS) and low-alcohol-sensitive (LAS) rats were bred for sensitivity and insensitivity, respectively, to the sedative/hypnotic effects of ethanol. These rats also display differential sensitivity to the depressant effects of locally applied ethanol on cerebellar Purkinje neurons in vivo. We have found that LAS animals exhibit a greater influence of endogenous β–adrenergic activity on neuronal responses to γ-aminobutyric acid (GABA) and ethanol than do HAS animals. In the current study, we investigated the possibility that the regulation of synaptic norepinephrine levels by norepinephrine transporters could contribute to a differential β–adrenergic influence on GABA and ethanol sensitivity between HAS and LAS rats. We locally applied norepinephrine from a glass micropipette into the various layers of cerebellar brain slices prepared from LAS and HAS rats, and recorded the levels of norepinephrine clearance by using Nafion-coated carbon-fiber microelectrodes. Norepinephrine clearance was significantly faster by ∼64% in the Purkinje cell layer of HAS rats. No differences in norepinephrine clearance were found in the molecular or the granule layer between LAS and HAS rats. The catecholamine uptake inhibitor nomifensine reduced norepinephrine clearance in both rat lines. These findings support the hypothesis that regulation of synaptic norepinephrine levels by norepinephrine transporter activity in the Purkinje cell layer may contribute to the differential sensitivity of Purkinje neurons to ethanol and GABA in LAS and HAS rats.

Keywords:  Norepinephrine transporters, Cerebellum, Ethanol, Genetic selection

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 A paper published as a high-priority communication is one that reviewers have identified as being of high scientific significance and have recommended that the study findings should be communicated to the scientific community as soon as possible.

PII: S0741-8329(03)00098-3

doi:10.1016/S0741-8329(03)00098-3

Alcohol
Volume 30, Issue 1 , Pages 9-18, May 2003