Journal
STEROIDS
Volume 190, Issue -, Pages -Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.steroids.2022.109155
Keywords
Chronic constriction injury; Hyperalgesia; Allodynia; Progesterone; Ephrin-B2
Ask authors/readers for more resources
Recent studies have shown that the ephrin/Eph signaling pathway may contribute to the pathology of neuropathic pain. Progesterone, administered after nerve injury, can alleviate neuropathic pain by suppressing the activation of ephrin-B2. The expression of spinal ephrin-B2 increased after nerve injury, and the administration of progesterone decreased mechanical allodynia, thermal hyperalgesia, and the expression of ephrin-B2.
Recent studies have shown that the ephrin/Eph signaling pathway may contribute to the pathology of neuro-pathic pain. Drugs like progesterone may be used to counteract both thermal hyperalgesia and mechanical allodynia in different models of neuropathic pain. The present study was designed to determine progesterone's modulatory role on neuropathic pain and spinal expression of ephrin-B2 following chronic constriction nerve injury (CCI).Thirty-six adult male Wistar rats were used. The sciatic nerve was chronically constricted. Progesterone (5 mg/ kg and 15 mg/kg) was administrated for 10 days (from day 1 up to day10) following sciatic constriction. Behavioral tests were performed before surgery (day 0) and on days 1, 3, 7, and 14 after CCI and before pro-gesterone administration on the same days. Western blotting was performed on days 3, 7, and 14th post-surgery. The findings showed that after CCI, the expression of spinal cord ephrin-B2 increased significantly in parallel with mechanical allodynia and thermal hyperalgesia. Post-injury administration of progesterone (15 mg/kg but not 5) decreased mechanical allodynia, thermal hyperalgesia, and the expression of spinal ephrin-B2.It is concluded that post-injury repeated administration of progesterone could be an effective way of allevi-ating neuropathic pain by suppressing ephrin-B2 activation and helps to make the better design of steroid-based therapies to inhibit pain after peripheral injury.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available