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Missouri State University

The Effect of Cholecystokinin Antagonist Lorglumide on Dopamine Levels in the Rat Caudate

Abstract

dc:description.abstract

Systemic administration of the CCK-A receptor antagonist lorglumide has been shown to block voltammetrically detected dopamine (DA) signals associated with slow wave depolarization (SWD) in the rat caudate (CPu). Failure to elicit KC1-induced DA signals following lorglumide treatment may be due to a CCK-DA interaction. This possibility was investigated in this study using both turnover estimates and microdialysis to evaluate the effects of systemic lorglumide on DA turnover and release in the rat CPu. Turnover estimates based on the depletion of DA following α-mpt or by evaluation of DOPAC/DA ratios failed to reveal a significant difference when lorglumide-treated animals were compared to saline treated controls. Further, lorglumide did not alter basal or KC1-stimulated DA and serotonin release in the CPu as measured by microdialysis. These results suggest that any potential interaction between CCK and DA in the rat CPu is not mediated by CCK-A receptors.

Degree

thesis:*
Name thesis:degree_name
Master of Science in Biology
Level thesis:degree_level
Masters
Discipline thesis:degree_discipline
Biology
Year
1993

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Kedzie, Kathleen A.
Contributors dc:contributor
  • Kenneth Renner

Subjects

dc:subject × 1

Rights

dc:rights
Statement dc:rights
  • © Kathleen A Kedzie

Identifiers

dc:identifier.*
Repository record dc:identifier
https://bearworks.missouristate.edu/theses/152
OAI identifier oai:identifier
oai:bearworks.missouristate.edu:theses-1153

Chain of custody

source
Harvested from
Missouri State University
Base URL
bearworks.missouristate.edu/do/oai/
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
related terms
citation

Kedzie, Kathleen A.. The Effect of Cholecystokinin Antagonist Lorglumide on Dopamine Levels in the Rat Caudate. Masters thesis, 1993. https://bearworks.missouristate.edu/theses/152