Abstract | OBJECTIVES: RESULTS: The study determined that the PPARγ nuclear receptor plays a significant role in trigeminal nociception transmission, evidenced by: 1) Intense PPARγ immunoreactivity is expressed 3 weeks after TIC nerve injury in the spinal trigeminal caudalis, the termination site of trigeminal nociceptive nerve fibers. 2) Systemic administration of a PPARγ agonist, pioglitazone (PIO), attenuates whisker pad mechanical allodynia at doses of 300 mg/kg i.p. and 600 mg/kg p.o. 3) Administration of a PPARγ antagonist, GW9662 (30 mg/kg i.p.), prior to providing the optimal dose of PIO (300 mg/kg i.p.) blocked the analgesic effect of PIO. DISCUSSION: This is the first study localizing PPARγ immunoreactivity throughout the brainstem trigeminal sensory spinal nucleus (spV) and its increase three weeks after TIC nerve injury. This is also the first study to demonstrate that activation of PPARγ attenuates trigeminal hypersensitivity in the mouse TIC nerve injury model. The findings presented here suggest the possibility of utilizing the FDA approved diabetic treatment drug, PIO, as a new therapeutic that targets PPARγ for treatment of patients suffering from orofacial neuropathic pain.
|
Authors | Danielle N Lyons, Liping Zhang, Robert J Danaher, Craig S Miller, Karin N Westlund |
Journal | The Clinical journal of pain
(Clin J Pain)
Vol. 33
Issue 12
Pg. 1071-1080
(12 2017)
ISSN: 1536-5409 [Electronic] United States |
PMID | 28514232
(Publication Type: Journal Article)
|
Chemical References |
- 2-chloro-5-nitrobenzanilide
- Analgesics, Non-Narcotic
- Anilides
- PPAR alpha
- PPAR delta
- PPAR gamma
- Thiazolidinediones
- Pioglitazone
|
Topics |
- Analgesics, Non-Narcotic
(pharmacology)
- Anilides
(pharmacology)
- Animals
- Disease Models, Animal
- Facial Pain
(drug therapy, pathology, physiopathology)
- Hyperalgesia
(pathology, physiopathology)
- Male
- Mice, Inbred C57BL
- Neuralgia
(drug therapy, pathology, physiopathology)
- PPAR alpha
(agonists, metabolism)
- PPAR delta
(agonists, metabolism)
- PPAR gamma
(agonists, antagonists & inhibitors, metabolism)
- Pioglitazone
- Random Allocation
- Thiazolidinediones
(pharmacology)
- Trigeminal Nerve Injuries
(drug therapy, pathology, physiopathology)
- Trigeminal Nuclei
(drug effects, metabolism, pathology)
- Vibrissae
|