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Anandamide content is increased and CB1 cannabinoid receptor blockade is protective during transient, focal cerebral ischemia.
Neuroscience. 2004; 129(3):743-50.N

Abstract

The role of endocannabinoid signaling in the response of the brain to injury is tantalizing but not clear. In this study, transient middle cerebral artery occlusion (MCAo) was used to produce ischemia/reperfusion injury. Brain content of N-arachidonoylethanolamine (AEA) and 2-arachidonoylglycerol were determined during MCAo. Whole brain AEA content was significantly increased after 30, 60 and 120 min MCAo compared with sham-operated brain. The increase in AEA was localized to the ischemic hemisphere after 30 min MCAo, but at 60 and 120 min, was also increased in the contralateral hemisphere. 2-Arachidonoylglycerol content was unaffected by MCAo. In a second set of studies, injury was assessed 24 h after 2 h MCAo. Rats administered a single dose (3 mg/kg) of the cannabinoid receptor type 1 (CB1) receptor antagonist SR141716 prior to MCAo exhibited a 50% reduction in infarct volume and a 40% improvement in neurological function compared with vehicle control. A second CB1 receptor antagonist, LY320135 (6 mg/kg), also significantly improved neurological function. The CB1 receptor agonist, WIN 55212-2 (0.1-1 mg/kg) did not affect either infarct volume or neurological score.

Authors+Show Affiliations

Department of Pharmacology and Toxicology, Medical College of Wisconsin, 8701 Watertown Planck Road, Milwaukee, WI 53226, USA. shanmugam.muthian@pfizer.comNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Comparative Study
Journal Article
Research Support, U.S. Gov't, P.H.S.

Language

eng

PubMed ID

15541895

Citation

Muthian, S, et al. "Anandamide Content Is Increased and CB1 Cannabinoid Receptor Blockade Is Protective During Transient, Focal Cerebral Ischemia." Neuroscience, vol. 129, no. 3, 2004, pp. 743-50.
Muthian S, Rademacher DJ, Roelke CT, et al. Anandamide content is increased and CB1 cannabinoid receptor blockade is protective during transient, focal cerebral ischemia. Neuroscience. 2004;129(3):743-50.
Muthian, S., Rademacher, D. J., Roelke, C. T., Gross, G. J., & Hillard, C. J. (2004). Anandamide content is increased and CB1 cannabinoid receptor blockade is protective during transient, focal cerebral ischemia. Neuroscience, 129(3), 743-50.
Muthian S, et al. Anandamide Content Is Increased and CB1 Cannabinoid Receptor Blockade Is Protective During Transient, Focal Cerebral Ischemia. Neuroscience. 2004;129(3):743-50. PubMed PMID: 15541895.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Anandamide content is increased and CB1 cannabinoid receptor blockade is protective during transient, focal cerebral ischemia. AU - Muthian,S, AU - Rademacher,D J, AU - Roelke,C T, AU - Gross,G J, AU - Hillard,C J, PY - 2004/08/25/accepted PY - 2004/11/16/pubmed PY - 2005/3/8/medline PY - 2004/11/16/entrez SP - 743 EP - 50 JF - Neuroscience JO - Neuroscience VL - 129 IS - 3 N2 - The role of endocannabinoid signaling in the response of the brain to injury is tantalizing but not clear. In this study, transient middle cerebral artery occlusion (MCAo) was used to produce ischemia/reperfusion injury. Brain content of N-arachidonoylethanolamine (AEA) and 2-arachidonoylglycerol were determined during MCAo. Whole brain AEA content was significantly increased after 30, 60 and 120 min MCAo compared with sham-operated brain. The increase in AEA was localized to the ischemic hemisphere after 30 min MCAo, but at 60 and 120 min, was also increased in the contralateral hemisphere. 2-Arachidonoylglycerol content was unaffected by MCAo. In a second set of studies, injury was assessed 24 h after 2 h MCAo. Rats administered a single dose (3 mg/kg) of the cannabinoid receptor type 1 (CB1) receptor antagonist SR141716 prior to MCAo exhibited a 50% reduction in infarct volume and a 40% improvement in neurological function compared with vehicle control. A second CB1 receptor antagonist, LY320135 (6 mg/kg), also significantly improved neurological function. The CB1 receptor agonist, WIN 55212-2 (0.1-1 mg/kg) did not affect either infarct volume or neurological score. SN - 0306-4522 UR - https://www.unboundmedicine.com/medline/citation/15541895/Anandamide_content_is_increased_and_CB1_cannabinoid_receptor_blockade_is_protective_during_transient_focal_cerebral_ischemia_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0306-4522(04)00768-7 DB - PRIME DP - Unbound Medicine ER -