Volume 40, Issue 11 pp. 1523-1528

Anticonvulsant Activity of PNU-151774E1 in the Amygdala Kindled Model of Complex Partial Seizures

Roberto Maj

Corresponding Author

Roberto Maj

Newron Pharmaceuticals Gerenzano (VA)

Address/Correspondence and reprint requests to Dr. R. Maj at Newron Pharmaceuticals, Via Lepetit, 34, 21040 Gerenzano (VA), Italy.Search for more papers by this author
Ruggero G. Fariello

Ruggero G. Fariello

Newron Pharmaceuticals Gerenzano (VA)

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Paolo Pevarello

Paolo Pevarello

CNS Preclinical Research, Pharmacia & Upjohn, Nerviano, (MI), Italy

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Mario Varasi

Mario Varasi

CNS Preclinical Research, Pharmacia & Upjohn, Nerviano, (MI), Italy

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Robert A. McArthur

Robert A. McArthur

CNS Preclinical Research, Pharmacia & Upjohn, Nerviano, (MI), Italy

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Patricia Salvati

Patricia Salvati

Newron Pharmaceuticals Gerenzano (VA)

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First published: 02 August 2005
Citations: 22
1

Now changed to NW-1015.

Abstract

Summary: Purpose: PNU-151774E [(S)-(+)-2-(4-(3-fluoro-benzyloxy) benzylamino) propanamide, methanesulfonate] is a novel antiepileptic drug (AED) with a broad spectrum of activity in a variety of chemically and mechanically induced seizures. The objective of this study was to evaluate the activity of PNU-151774E in the amygdala fully kindled rat model of complex partial seizures, and to compare its effects with those of carbamazepine (CBZ), phenytoin (PHT), lamotrigine (LTG), and gabapentin (GBP), drugs used to treat this disease state.

Methods: Male Wistar rats were stimulated daily through electrodes implanted in the amygdala with a threshold current until fully generalized seizures developed. The rats were then treated with various doses of a single compound. Control values for each rat and drug dose were determined after vehicle administration followed by electrical stimulation 1 day before drug treatment.

Results: PNU-151774E (1, 10, 30 mg/kg; i.p.) reduced the duration of behavioral seizures significantly and dose-dependently at doses starting from 1 mg/kg. Higher doses significantly reduced seizure severity and afterdischarge duration. In contrast, no dose-related effects were noted after administration of PHT, whereas after CBZ treatment, a plateau of activity was noted from the intermediate to higher doses. The effects of PNU-151774E were comparable to those of LTG and GBP.

Conclusions: The activity shown by PNU-151774E at doses similar to those that are active in models of generalized seizures indicates that PNU-151774E would also have potential efficacy in the treatment of complex partial seizures.

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