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[Central effects of iohexol and iopamidol, non-ionic contrast media]
K Kisara1, S Sakurada, T Tadano
1Department of Pharmacology, Tohoku College of Pharmacy, Sendai, Japan.
Insights
Iohexol and iopamidol, commonly used contrast agents, showed distinct central nervous system effects in mice, including hypothermia and altered activity, suggesting varied pharmacological actions despite similar LD50 values.
Area of Science:
- Pharmacology
- Neuroscience
- Toxicology
Background:
- Iohexol and iopamidol are widely used iodinated contrast media.
- Their central nervous system (CNS) effects require thorough investigation.
Purpose of the Study:
- To compare the central nervous system effects of intravenously administered iohexol and iopamidol in mice.
- To evaluate potential differences in their pharmacological actions.
Main Methods:
- Comparative study using iohexol, iopamidol, and mannitol as a reference in ddY and ICR mice.
- Assessment of neurological and physiological parameters including startle response, locomotor activity, narcosis potentiation, hypothermia, mortality under electric stimulus, and tests for anticonvulsant, electroencephalic, muscle relaxant, and antinociceptive activities.
Main Results:
- No significant differences in startle response compared to mannitol.
- Iopamidol inhibited locomotor activity; iohexol potentiated thiopental-induced narcosis.
- High doses of both agents caused hypothermia and increased mortality with electric stimulus.
- No notable CNS activities were observed in anticonvulsant, electroencephalic, muscle relaxant, or antinociceptive tests.
Conclusions:
- Iohexol and iopamidol do not exhibit identical pharmacological profiles on the central nervous system.
- Despite high LD50 values (approx. 15000 mgI/kg), specific CNS effects warrant consideration.
- Further research may be needed to fully elucidate their neuropharmacological properties.
Abstract:
Central effects of intravenously (i.v.)-administered iohexol were compared with those of iopamidol in a series of tests. Mannitol was used as a reference. As assayed by the primary screening test based on Irwin's method, i.v. administration of mannitol resulted in a score of 0 in ddY mice and a score of 0.6 in ICR mice in the startle response. These results were not different from the data of both iohexol and iopamidol. Iopamidol at a dose of 1750 mgI/kg produced an inhibitory effect on the spontaneous locomotor activity. Iohexol at a dose of 7000 mgI/kg potentiated the duration of thiopental-induced narcosis. Hypothermia was caused by high doses of both iohexol and iopamidol. Electric stimulus increased the mortality of mice pretreated with high doses of iohexol and iopamidol. Both drugs had no notable activities in the anticonvulsant, electroencephalic, muscle relaxant and antinociceptive tests. These results indicate that both iohexol and iopamidol do not necessarily possess a similar pharmacological action. Judging from the LD50 of approximately 15000 mgI/kg for both drugs, they seem unlikely to have a specific pharmacological action on the central nervous system.
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