The past several years have seen an alarming increase in the abuse of centrally acting sympathomimetic stimulants and an increase in the incidence of cardiovascular toxicity. Due to the close temporal relationship between drug use and the onset of most clinically significant toxicities, most reports of the cardiovascular effects of these drugs have focused on the acute toxic responses. Very little attention has been paid to the possibility that repeated stimulant use may alter cardiovascular function in such a way as to increase the potential for the development of serious cardiovascular toxicity. Therefore, this proposal was designed to test the hypothesis that the repeated administration of sympathomimetic stimulants produces structural and/or functional changes in the cardiovascular system that increase the potential for the development of serious cardiovascular toxicity. These studies will attempt to determine whether the repeated administration of cocaine, 3,4-methylenedioxymethamphetamine (MDMA) or methamphetamine (METH) alters arterial pressure, heart rate, electrocardiographic activity size and baroreceptor or Bezold-Jarisch reflex function. Histologic and morphometric analysis will also be performed to determine whether repeated stimulant administration produces damage or structural changes in the heart that are visible at the light or electron microscopic level. Two types of dosing schedules will be employed. One will involve administration of cocaine, METH or MDMA on a daily basis for up to 2 months. The other type of schedule will involve large, closely spaced doses given for 4-14 days. The latter types of stimulant dosing schedule is similar to those often used to produce neurotoxicity in monoaminergic systems. The proposed studies represent a unique combination of """"""""state of the art"""""""" techniques for cardiovascular recording in conscious animals and histological analysis to examine the changes in cardiac, cardiovascular and cardiovascular reflex structure/function elicited by the repeated administration of sympathomimetic stimulants. Examination of these changes should provide new insight into the potential for repeated stimulant use to produce cardiac and/or cardiovascular toxicity. The mechanisms mediating these changes will provide the basis for future studies.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA008255-06
Application #
6175703
Study Section
Human Development Research Subcommittee (NIDA)
Program Officer
Thadani, Pushpa
Project Start
1994-02-15
Project End
2002-07-31
Budget Start
2000-08-01
Budget End
2002-07-31
Support Year
6
Fiscal Year
2000
Total Cost
$170,943
Indirect Cost
Name
Louisiana State Univ Hsc New Orleans
Department
Pharmacology
Type
Schools of Medicine
DUNS #
782627814
City
New Orleans
State
LA
Country
United States
Zip Code
70112
Shenouda, S K; Carvalho, F; Varner, K J (2010) The cardiovascular and cardiac actions of ecstasy and its metabolites. Curr Pharm Biotechnol 11:470-5
Hicks, Alissa R; Ogden, Brian A; Varner, Kurt J (2003) Cardiovascular responses elicited during binge administration of cocaine. Physiol Behav 80:115-22
Varner, Kurt J; Ogden, Brian A; Delcarpio, Joseph et al. (2002) Cardiovascular responses elicited by the ""binge"" administration of methamphetamine. J Pharmacol Exp Ther 301:152-9
Varner, K J; Hein, N D; Ogden, B A et al. (2001) Chloroephedrine: contaminant of methamphetamine synthesis with cardiovascular activity. Drug Alcohol Depend 64:299-307
O'Cain, P A; Hletko, S B; Ogden, B A et al. (2000) Cardiovascular and sympathetic responses and reflex changes elicited by MDMA. Physiol Behav 70:141-8
Cabral, A D; Kapusta, D R; Kenigs, V A et al. (1998) Central alpha2-receptor mechanisms contribute to enhanced renal responses during ketamine-xylazine anesthesia. Am J Physiol 275:R1867-74
Petersen, J S; Liu, W; Kapusta, D R et al. (1997) Metformin inhibits ganglionic neurotransmission in renal nerves. Hypertension 29:1173-7
Cabral, A M; Varner, K J; Kapusta, D R (1997) Renal excretory responses produced by central administration of opioid agonists in ketamine and xylazine-anesthetized rats. J Pharmacol Exp Ther 282:609-16
Abrahams, T P; Cuntapay, M; Varner, K J (1996) Sympathetic nerve responses elicited by cocaine in anesthetized and conscious rats. Physiol Behav 59:109-15
Abrahams, T P; Liu, W; Varner, K J (1996) Blockade of alpha-2 adrenergic receptors in the rostral ventrolateral medulla attenuates the sympathoinhibitory response to cocaine. J Pharmacol Exp Ther 279:967-74

Showing the most recent 10 out of 12 publications