Attenuation of PTZ Induced Generalized Clonic and Myoclonic Seizures by Meloxicam

Background: Millions of people worldwide suffer from epilepsy, a condition marked by repeated seizures, with about one-third of patients not being well controlled by the antiepileptic medications now on the market. In experimental settings, the Pentylenetetrazol (PTZ) model is frequently employed to cause seizures, offering a framework for assessing possible therapies. Since inflammation is a key factor in the epilepsy etiology, nonsteroidal anti-inflammatory medications (NSAIDs) with specific COX-2 inhibitors like meloxicam may have neuroprotective effects. Objective: To evaluate meloxicam's anticonvulsant qualities in a mouse model of PTZ-induced seizures is the main aim of this study. Materials & Methods: Five groups of male NAVAL MEDICAL RESEARCH INSTITUTE(NMRI) mice were established: control, diazepam + PTZ, meloxicam (25 mg/kg) + PTZ, meloxicam (15mg/kg) + PTZ, and PTZ only. Tukey and ANOVA's post-hoc test were used for the statistical analysis of the observed parameters for seizure onset, duration, severity, and post-seizure outcomes. Results: When compared to the PTZ-only group, meloxicam exhibited improved survival rates, decreased seizure length and severity, and markedly delayed the start of the first myoclonic jerk and generalized seizures. With a 90% survival rate, the high-dose meloxicam group (15 mg/kg) showed the most noticeable effects. Discussion: In the acute PTZ model, meloxicam significantly reduced the occurrence of generalized clonic and myoclonic seizures, indicating its potent anticonvulsant effects. This outcome is likely due to meloxicam’s COX-2 inhibition and TgF beta inhibition, which reduces the neuroinflammation and stabilizes neuronal excitability. By lowering pro-inflammatory prostaglandins that contribute to seizure susceptibility, meloxicam not only modulates seizure activity but may also offer neuroprotective benefits. These findings suggest meloxicam’s potential as a therapeutic option in epilepsy. Conclusion: Meloxicam has demonstrated potential as an anticonvulsant medication in PTZ-induced seizures, indicating the need for additional research into its long-term effectiveness and procedures of action in the epilepsy’streatment.

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Journal
RADS Journal of Pharmacy and Allied Health Sciences
Published
2025-01-09
DOI
https://doi.org/10.37962/jphs.v2i3.127
Primary Topic
Cancer Treatment and Pharmacology
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article
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article

Attenuation of PTZ Induced Generalized Clonic and Myoclonic Seizures by Meloxicam

Md. Shahid Jamal, Shabana Usman Sımjee, Shafqat Hussain, Uzair Nisar
RADS Journal of Pharmacy and Allied Health Sciences
Cancer Treatment and Pharmacology
article

Attenuation of PTZ Induced Generalized Clonic and Myoclonic Seizures by Meloxicam

Md. Shahid Jamal, Shabana Usman Sımjee, Shafqat Hussain, Uzair Nisar
article en

Abstract

Background: Millions of people worldwide suffer from epilepsy, a condition marked by repeated seizures, with about one-third of patients not being well controlled by the antiepileptic medications now on the market. In experimental settings, the Pentylenetetrazol (PTZ) model is frequently employed to cause seizures, offering a framework for assessing possible therapies. Since inflammation is a key factor in the epilepsy etiology, nonsteroidal anti-inflammatory medications (NSAIDs) with specific COX-2 inhibitors like meloxicam may have neuroprotective effects. Objective: To evaluate meloxicam's anticonvulsant qualities in a mouse model of PTZ-induced seizures is the main aim of this study. Materials & Methods: Five groups of male NAVAL MEDICAL RESEARCH INSTITUTE(NMRI) mice were established: control, diazepam + PTZ, meloxicam (25 mg/kg) + PTZ, meloxicam (15mg/kg) + PTZ, and PTZ only. Tukey and ANOVA's post-hoc test were used for the statistical analysis of the observed parameters for seizure onset, duration, severity, and post-seizure outcomes. Results: When compared to the PTZ-only group, meloxicam exhibited improved survival rates, decreased seizure length and severity, and markedly delayed the start of the first myoclonic jerk and generalized seizures. With a 90% survival rate, the high-dose meloxicam group (15 mg/kg) showed the most noticeable effects. Discussion: In the acute PTZ model, meloxicam significantly reduced the occurrence of generalized clonic and myoclonic seizures, indicating its potent anticonvulsant effects. This outcome is likely due to meloxicam’s COX-2 inhibition and TgF beta inhibition, which reduces the neuroinflammation and stabilizes neuronal excitability. By lowering pro-inflammatory prostaglandins that contribute to seizure susceptibility, meloxicam not only modulates seizure activity but may also offer neuroprotective benefits. These findings suggest meloxicam’s potential as a therapeutic option in epilepsy. Conclusion: Meloxicam has demonstrated potential as an anticonvulsant medication in PTZ-induced seizures, indicating the need for additional research into its long-term effectiveness and procedures of action in the epilepsy’streatment.

RADS Journal of Pharmacy and Allied Health SciencesVol. 2(3)
University of Karachi (PK), City University of Science and Information Technology (PK), International Center for Chemical and Biological Sciences (PK)
Openalex Percentile: Top 73%
Cancer Treatment and Pharmacology
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