Cannabinoid signaling may ease stress-linked jaw pain

Endocannabinoid system attenuates emotional stress-induced orofacial musculoskeletal pain in rats.

Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas β€’ β€’ Highly Relevant
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AI Summary

Researchers studied whether the endocannabinoid system helps regulate jaw and facial muscle pain triggered by emotional stress. In male rats, stress increased mechanical sensitivity in the chewing muscles and increased c-Fos, a marker associated with neural activation, in pain-related regions including the trigeminal ganglion and trigeminal nucleus caudalis.

Blocking either CB1 or CB2 receptors made the stress-related pain response worse, while activating cannabinoid receptors with WIN55,212-2 reduced it. Stress also increased cannabinoid receptor levels in several pain-related tissues. The findings suggest that cannabinoid signaling may protect against stress-induced orofacial pain, supporting further research into endocannabinoid system modulation for temporomandibular disorders. However, this was an animal study, and the abstract does not provide quantitative effect sizes or evidence that cannabis products relieve jaw pain in people.

πŸ’‘ Key Findings

1
Emotional stress increased mechanical sensitivity in the rats’ masticatory muscles, indicating greater orofacial musculoskeletal pain.
Moderate
45%
2
Blocking either CB1 or CB2 receptors increased mechanical sensitivity, while activating cannabinoid receptors reduced stress-related pain.
Moderate
45%
3
Stress altered CB1 and CB2 receptor expression in pain-related tissues, including the trigeminal ganglion, trigeminal nucleus caudalis, and masseter muscle.
Moderate
45%
4
The results suggest that cannabinoid receptors play a protective role in stress-induced orofacial pain, but the evidence is currently limited to rats.
Moderate
45%

πŸ“„ Original Abstract

Orofacial musculoskeletal pain (OMP) is a common feature of temporomandibular disorders (TMD), a group of conditions affecting the temporomandibular joint, chewing muscles, and associated structures. The etiology of muscular TMD is currently understood within a biopsychosocial model of pain, highlighting the complexity related to OMP. In this context, the objective of this study was to investigate the OMP induced by psychological/emotional stress (ES) in rats, regarding the role of the endocannabinoid system (ECS) through CB1 and CB2 receptors. Male Wistar rats were divided into Control and ES groups. OMP was induced by ES using the communication box model and evaluated through the mechanical threshold in masticatory muscles. c-Fos, CB1, and CB2 immunostaining was evaluated in the trigeminal ganglion (TG) and in the trigeminal nucleus caudalis (Sp5C). The selective CB1 or CB2 antagonist (AM251 or AM630, respectively) or the cannabinoid receptor non-selective agonist (WIN55,212-2) were administered to both groups, and the OMP was evaluated. The mechanical sensitivity of the masticatory muscles increased in the ES group, accompanied by increased c-Fos expression in the TG and Sp5C. AM251 and AM630 increased mechanical sensitivity, while WIN55,212-2 decreased the OMP. Furthermore, ES increased CB1 density in the TG and elevated both CB1 and CB2 in the Sp5C. Additionally, CB2 was increased in the masseter muscle. Thus, cannabinoid receptors played a protector role in OMP caused by ES, indicating that cannabinoid drugs or the modulation of the ECS may represent a promising approach for the treatment of OMP frequently observed in patients with TMD.

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