Effect of vasoconstrictive agents added to lidocaine on intravenous lidocaine-induced convulsions in rats
- PMID: 7856916
- DOI: 10.1097/00000542-199502000-00028
Effect of vasoconstrictive agents added to lidocaine on intravenous lidocaine-induced convulsions in rats
Abstract
Background: Epinephrine is reported to decrease the threshold of intravenous lidocaine-induced convulsions. However, the mechanism underlying this effect is not clear. Therefore, we carried out a study to examine the role of vasopressor-induced hypertension.
Methods: Fifty-six awake Wistar rats were assigned to seven groups of eight. All groups received a continuous intravenous infusion of lidocaine at a rate of 4 mg.kg-1.min-1 until generalized convulsions occurred. The control group (group C) received plain lidocaine. The acute hypertensive groups received lidocaine with epinephrine (group E), norepinephrine (group N), or phenylephrine (group P) to increase mean arterial blood pressure (MAP) to 150 +/- 5 mmHg. Sodium nitroprusside (SNP) was added to prevent an increase in mean arterial pressure in the remaining three groups (vasopressor-SNP groups).
Results: The acute hypertensive groups required significantly smaller cumulative doses of lidocaine to produce convulsions compared with control (C = 41.5 +/- 2.9 > E = 24.1 +/- 2.7, N = 27.1 +/- 2.8, P = 26.7 +/- 2.5 mg.kg-1; values are mean +/- SD, P < 0.01). In addition, plasma lidocaine concentrations (C = 11.0 +/- 0.7 > E = 7.4 +/- 0.5, N = 7.9 +/- 0.6, P = 8.1 +/- 0.8 micrograms.ml-1, P < 0.01) and brain lidocaine concentrations (C = 50.9 +/- 4.5 > E = 32.6 +/- 4.2, N = 34.5 +/- 4.8, P = 37.1 +/- 4.5 micrograms.g-1, P < 0.01) were less in the acute hypertensive groups at the onset of convulsions. In the vasopressor-SNP groups, the plasma and brain lidocaine concentrations at the onset of convulsions returned to the control values, although epinephrine and norepinephrine, but not phenylephrine, still decreased cumulative convulsant doses of lidocaine significantly (P < 0.01) compared with control (E + SNP = 30.8 +/- 2.9 < N + SNP = 34.8 +/- 2.8, P < 0.01) < P + SNP = 40.2 +/- 3.0 mg.kg-1, P < 0.01). The brain/plasma concentration ratios were similar for the seven groups.
Conclusions: An equal degree of acute hypertension induced by these three different vasopressors may play a role in reducing the threshold (plasma and brain lidocaine concentrations) as well as the cumulative convulsant doses associated with lidocaine-induced convulsions.
Similar articles
-
Modification of intravenous lidocaine-induced convulsions by epinephrine in rats.Can J Anaesth. 1993 Mar;40(3):251-6. doi: 10.1007/BF03037037. Can J Anaesth. 1993. PMID: 8467547
-
Clonidine does not affect lidocaine seizure threshold in rats.Can J Anaesth. 1993 Dec;40(12):1205-9. doi: 10.1007/BF03009611. Can J Anaesth. 1993. PMID: 8281598
-
Effects of flumazenil on intravenous lidocaine-induced convulsions and anticonvulsant property of diazepam in rats.Anesth Analg. 1992 Jul;75(1):87-90. doi: 10.1213/00000539-199207000-00016. Anesth Analg. 1992. PMID: 1319692
-
The effects of exogenous epinephrine on a convulsive dose of lidocaine: relationship with cerebral circulation.J Neurosurg Anesthesiol. 1998 Jul;10(3):178-87. doi: 10.1097/00008506-199807000-00009. J Neurosurg Anesthesiol. 1998. PMID: 9681407
-
Does Low Dose Lidocaine Cause Convulsions?Turk J Anaesthesiol Reanim. 2014 Apr;42(2):106-8. doi: 10.5152/TJAR.2014.21043. Epub 2014 Jan 6. Turk J Anaesthesiol Reanim. 2014. PMID: 27366401 Free PMC article. Review.
Cited by
-
Cardiorespiratory and antinociceptive effects of two different doses of lidocaine administered to horses during a constant intravenous infusion of xylazine and ketamine.BMC Vet Res. 2013 Oct 9;9:199. doi: 10.1186/1746-6148-9-199. BMC Vet Res. 2013. PMID: 24103634 Free PMC article. Clinical Trial.
-
Adverse effects and drug interactions associated with local and regional anaesthesia.Drug Saf. 1998 Apr;18(4):221-50. doi: 10.2165/00002018-199818040-00001. Drug Saf. 1998. PMID: 9565736 Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous