COMPARATIVE SYSTEMIC TOXICITY AND A MECHANISM FOR LETHALITY OF INTRAVENOUSLY INFUSED COCAINE, LIDOCAINE, AND BUPIVACAINE IN SPONTANEOUSLY AND MECHANICALLY BREATHING UNCONSCIOUS PIGS

Citation
Jr. Kambam et al., COMPARATIVE SYSTEMIC TOXICITY AND A MECHANISM FOR LETHALITY OF INTRAVENOUSLY INFUSED COCAINE, LIDOCAINE, AND BUPIVACAINE IN SPONTANEOUSLY AND MECHANICALLY BREATHING UNCONSCIOUS PIGS, Research communications in substance abuse, 14(2-3), 1993, pp. 97-112
Citations number
25
Categorie Soggetti
Substance Abuse
ISSN journal
01930818
Volume
14
Issue
2-3
Year of publication
1993
Pages
97 - 112
Database
ISI
SICI code
0193-0818(1993)14:2-3<97:CSTAAM>2.0.ZU;2-J
Abstract
We investigated systemic toxicity and possible mechanisms for lethalit y of intravenously (iv) infused cocaine (C), lidocaine (L), and bupiva caine (B) in 24 spontaneously and mechanically breathing unconscious p igs. Pigs were given sodium thiopental and ventilated with 70% nitrous oxide in 30% oxygen. Pigs in groups 1, 2, and 3 pigs were allowed to breathe spontaneously and groups 4, 5, and 6 were mechanically ventila ted. The animals in groups 1 and 4 were infused iv with C (0.8 mg/kg/m in), groups 2 and 5 were infused with B (0.8 mg/kg/min), and groups 3 and 6 were infused with L (3.2 mg/kg/min). Respiratory and cardiovascu lar parameters, blood temperature, sodium and potassium levels were mo nitored. The times of occurrences of respiratory (RA) and cardiac arre sts (CA), and convulsions were recorded. Our results showed that RA is the primary cause of death in spontaneously breathing pigs and that m echanical ventilation significantly delayed the occurrence of CA (p < 0.05). Significant decreases in cardiac output, mean blood pressure, a nd heart rate and significant increases in systemic and pulmonary vasc ular resistances, central venous and pulmonary wedge pressures, and bl ood K+ levels were noticed in mechanically ventilated pigs (p < 0.05). Our experiments demonstrated that all three local anesthetic drugs pr oduced similar systemic effects with continuous iv administration of l ethal doses.