Abstract | OBJECTIVES: METHODS: 64 male Naval Medical Research Institute (NMRI) mice weighing 25-29 g were randomly divided into eight experimental groups (n=8). FA at doses 5, 10, and 40 mg/kg alone and in combination with L-nitro- arginine methyl ester ( L-NAME) ( nitric oxide synthase inhibitor) or L-arginine (L-arg) ( nitric oxide [NO] precursor) was administrated (intraperitoneal). PTZ was injected (i.v. route) 30 min after drugs administration (1 mL/min). Seizure onset time was recorded and the nitrite levels of prefrontal cortex and serum were determined by the Griess method. RESULTS: FA at doses of 10 and 40 mg/kg significantly increased the seizure threshold as well as reduced the serum and brain NO levels in comparison to the saline-received group. Co-administration of the effective dose of FA (10 mg/kg) plus L-arg significantly decreased the seizure threshold in comparison to the effective dose of FA alone. Co-injection of the sub-effective dose of FA (5 mg/kg) with L-NAME significantly increased the seizure threshold as well as significantly decreased the brain NO level in comparison to the sub-effective dose of FA alone. CONCLUSIONS: We showed that the nitrergic system, partially at least, mediated the anticonvulsant effect of FA in PTZ-induced seizures in mice. We concluded that L-NAME potentiated while L-arg attenuated the anticonvulsant effect of FA.
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Authors | Hossein Amini-Khoei, Shakiba Nasiri Boroujeni, Zahra Lorigooini, Arash Salehi, Reihaneh Sadeghian, Mohammad Rahimi-Madiseh |
Journal | Journal of basic and clinical physiology and pharmacology
(J Basic Clin Physiol Pharmacol)
Vol. 34
Issue 2
Pg. 197-203
(Mar 01 2023)
ISSN: 2191-0286 [Electronic] Germany |
PMID | 34412169
(Publication Type: Journal Article)
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Copyright | © 2021 Walter de Gruyter GmbH, Berlin/Boston. |