CJA
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Résumé de cet Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a scholarly reply
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Park, H. J.
Right arrow Articles by Moon, D. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Park, H. J.
Right arrow Articles by Moon, D. E.
Canadian Journal of Anesthesia 53:470-477 (2006)
© Canadian Anesthesiologists' Society, 2006

Regional Anesthesia and Pain

The effects of botulinum toxin A on mechanical and cold allodynia in a rat model of neuropathic pain

[Les effets de la toxine botulique A sur l’allodynie mécanique et l’allodynie au froid chez un modèle de douleur neuropathique chez le rat]

Hue Jung Park, MD, Yoonki Lee, MD, Jaemin Lee, MD, Chongmin Park, MD and Dong Eon Moon, MD

From the Department of Anesthesiology and Pain Medicine, School of Medicine, The Catholic University of Korea, Seoul, Korea.

Address correspondence to: Dr. Dong Eon Moon, Department of Anesthesiology and Pain Medicine, School of Medicine, The Catholic University of Korea, Kangnam St. Mary’s Hospital, 505 Banpo-Dong, Seocho-Gu, Seoul, Korea, 137-040. Phone: 82-2-590-1545, 1537; Fax: 82-2-537-1951; E-mail: demoon{at}catholic.ac.kr

Purpose: Botulinum toxin type A (BoNT-A) has been used to treat many disorders related to excessive muscle contraction, but there are few studies evaluating its effects on neuropathic pain. The aim of this study was to evaluate the analgesic effects of BoNT-A in a rat model of neuropathic pain.

Methods: Male Sprague-Dawley rats were prepared by ligating the left L5 and L6 spinal nerves to produce neuropathic pain. Seventy neuropathic rats were randomly assigned into seven groups. Either normal saline or BoNT-A (10, 20, 30 and 40 U·kg–1) was administered to the plantar surface of the affected left hind paw, and BoNT-A (30 and 40 U·kg–1) was administered into the unaffected right paw in order to determine the drug-induced systemic effect. Mechanical and cold allodynia were observed at pre-administration, one, three, five, seven and 15 days after drug administration, and were quantified by measuring withdrawal frequencies to stimuli with von Frey filament and 100% acetone, respectively. Rotarod performance was measured to detect drug-induced adverse motor effects.

Results: The mean minimum withdrawal frequencies to mechanical and cold stimuli were 77 ± 11 and 90 ± 4.5%, 46 ± 5 and 66 ± 7%, 33 ± 7 and 62 ± 7%, 12 ± 2.9 and 54 ± 7.3% with 10, 20, 30 and 40 U·kg–1 BoNT-A respectively (P < 0.05). Doses of 30 and 40 U·kg–1 BoNT-A resulted in reduced rotarod performance time.

Conclusion: We conclude that peripherally administered BoNT-A reduces mechanical and cold allodynia in a rat model of neuropathic pain.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2006 by the Canadian Anesthesiologists' Society.