THE RAT MODEL OF TARDIVE-DYSKINESIA - RELATIONSHIP BETWEEN VACUOUS CHEWING MOVEMENTS AND GROSS MOTOR-ACTIVITY DURING ACUTE AND LONG-TERM HALOPERIDOL TREATMENT

Citation
Oa. Andreassen et Ha. Jorgensen, THE RAT MODEL OF TARDIVE-DYSKINESIA - RELATIONSHIP BETWEEN VACUOUS CHEWING MOVEMENTS AND GROSS MOTOR-ACTIVITY DURING ACUTE AND LONG-TERM HALOPERIDOL TREATMENT, Life sciences, 57(24), 1995, pp. 2263-2272
Citations number
27
Categorie Soggetti
Biology,"Medicine, Research & Experimental","Pharmacology & Pharmacy
Journal title
ISSN journal
00243205
Volume
57
Issue
24
Year of publication
1995
Pages
2263 - 2272
Database
ISI
SICI code
0024-3205(1995)57:24<2263:TRMOT->2.0.ZU;2-J
Abstract
Tardive dyskinesia (TD) is a serious side-effect of neuroleptic treatm ent. In order to describe and analyse more thoroughly the rat model of TD, the behavior of the rats during cage testing was studied after ac ute and during long-term haloperidol (HAL) treatment. Rats were inject ed with HAL TP in an acute experiment, and in a long-term experiment, rats were treated for 4-12 months with HAL decanoate LM. Control rats received saline or sesame oil. The behavior was videotaped one h after the IP injection in the acute experiment, and at intervals during the long-term experiment. The putative TD analogue vacuous chewing moveme nts (VCM), the general behavior and the type of behavior occurring sim ultaneously with VCM, were scored. Long-term (> 4 months) HAL treatmen t increased VCM but did not change the general behavior. The single IP injection of HAL markedly reduced locomotion in addition to increasin g VCM. Both in the acute and in the long-term experiment, VCM appeared more frequently when the gross motor activity was low, indicating an intrinsic incompatibility between gross motor activity and VCM. Howeve r, in the long-term experiment, the distribution of VCM in the differe nt categories of behavior was the same in OIL and HAL treated rats. Th is shows that cage-observed VCM in rats induced by long-term HAL treat ment cannot be an artifact due to reduced locomotion. Thereby, an impo rtant argument against cage-observed VCM as a rat model of TD seems to be disproved.