Effects of intraplantar administration of Complete Freund's Adjuvant (CFA) on rotarod performance in mice.

CFA mice pain rotarod von Frey

Journal

Scandinavian journal of pain
ISSN: 1877-8879
Titre abrégé: Scand J Pain
Pays: Germany
ID NLM: 101520867

Informations de publication

Date de publication:
25 Oct 2019
Historique:
received: 10 12 2018
accepted: 04 06 2019
pubmed: 3 7 2019
medline: 3 7 2019
entrez: 3 7 2019
Statut: epublish

Résumé

Preclinical animal models are crucial to study pain mechanisms and assess antinociceptive effects of medications. One major problem with current animal behavioral models is their lack of face validity with human nociception and the vulnerability for false-positive results. Here, we evaluated the usefulness of rotarod as a new way to assess inflammatory nociception in rodents. Adult male mice were injected with saline or Complete Freund's Adjuvant (CFA) in the left hindpaws. Mechanical allodynia and rotarod performance were evaluated before and after the administration of CFA. Mechanical allodynia was measured using von Frey filaments. Long-term effect of CFA on rotarod performance was also assessed for 2 weeks. Our results showed that CFA administration decreased pain threshold and increased sensitivity to von Frey filaments compared to control group. In rotarod experiments, the starting speed of the rod rotation started at four RPM, and accelerated until it reached 40 RPM in 5 min. Rotarod performance was enhanced from day to day in the control group. However, rotarod performance in CFA group was attenuated after CFA administration, which was significant after 24 h compared to vehicle. This attenuation was blocked by ibuprofen. Haloperidol administration (positive control) produced similar results to CFA administration. CFA did not produce significant attenuation of rotarod performance after 1 week post-injection. Collectively, our findings could encourage the use of rotarod assay to measure acute (but not chronic) inflammatory nociception as a useful tool in rodents.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Preclinical animal models are crucial to study pain mechanisms and assess antinociceptive effects of medications. One major problem with current animal behavioral models is their lack of face validity with human nociception and the vulnerability for false-positive results. Here, we evaluated the usefulness of rotarod as a new way to assess inflammatory nociception in rodents.
METHODS METHODS
Adult male mice were injected with saline or Complete Freund's Adjuvant (CFA) in the left hindpaws. Mechanical allodynia and rotarod performance were evaluated before and after the administration of CFA. Mechanical allodynia was measured using von Frey filaments. Long-term effect of CFA on rotarod performance was also assessed for 2 weeks.
RESULTS RESULTS
Our results showed that CFA administration decreased pain threshold and increased sensitivity to von Frey filaments compared to control group. In rotarod experiments, the starting speed of the rod rotation started at four RPM, and accelerated until it reached 40 RPM in 5 min. Rotarod performance was enhanced from day to day in the control group. However, rotarod performance in CFA group was attenuated after CFA administration, which was significant after 24 h compared to vehicle. This attenuation was blocked by ibuprofen. Haloperidol administration (positive control) produced similar results to CFA administration. CFA did not produce significant attenuation of rotarod performance after 1 week post-injection.
CONCLUSIONS CONCLUSIONS
Collectively, our findings could encourage the use of rotarod assay to measure acute (but not chronic) inflammatory nociception as a useful tool in rodents.

Identifiants

pubmed: 31265434
doi: 10.1515/sjpain-2018-0358
pii: /j/sjpain.ahead-of-print/sjpain-2018-0358/sjpain-2018-0358.xml
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

805-811

Informations de copyright

©2019 Scandinavian Association for the Study of Pain. Published by Walter de Gruyter GmbH, Berlin/Boston. All rights reserved.

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Auteurs

Ahmad Altarifi (A)

Department of Pharmacology, School of Medicine, Jordan University of Science and Technology, P.O. Box 3030, Irbid 22110, Jordan, Phone: +962 2 7201000/ext. 23864, Fax: +962 2 7095123.

Mohammad Alsalem (M)

Department of Anatomy and Histology, Faculty of Medicine, The University of Jordan, Amman 11942, Jordan.

Ayman Mustafa (A)

College of Medicine, Qatar University, Doha, Qatar.

Classifications MeSH