Modality-specific peripheral antinociceptive effects of μ-opioid agonists on heat and mechanical stimuli: Contribution of sigma-1 receptors

NEUROPHARMACOLOGY

卷:135

Article

Montilla-Garcia, Angeles^1,2  Perazzoli, Gloria^3,4  Tejada, Miguel A.^1,2  Gonzalez-Cano, Rafael^1,2  Sanchez-Fernandez, Cristina^1,2  Cobos, Enrique J.^1,2,5,6  Baeyens, Jose M.^1,2,5 

[1] Univ Granada, Fac Med, Dept Pharmacol, Ave Invest 11, E-18071 Granada, Spain

[2] Univ Granada, Biomed Res Ctr, Inst Neurosci, Parque Tecnol Ciencias Salud, Granada 18100, Spain

[3] Univ Granada, Fac Med, Dept Anat & Embryol, E-18071 Granada, Spain

[4] Univ Granada, Biomed Res Ctr, Inst Biopathol & Regenerat Med IBIMER, Parque Tecnol Ciencias Salud, Granada 18100, Spain

[5] Univ Hosp Complex Granada, Biosanit Res Inst, Granada 18012, Spain

[6] Teofilo Hernando Inst Drug Discovery, Madrid 28029, Spain

关键词: Sigma-1 receptors;    Opioid drugs;    Peripheral antinociception;    Mechanical stimulus;    Heat stimulus;    TRPV1-Expressing neurons;   

DOI  :  10.1016/j.neuropharm.2018.03.025

来源: Elsevier

【 摘 要 】

Morphine induces peripherally mu-opioid-mediated antinociception to heat but not to mechanical stimulation. Peripheral sigma-1 receptors tonically inhibit mu-opioid antinociception to mechanical stimuli, but it is unknown whether they modulate mu-opioid heat antinociception. We hypothesized that sigma-1 receptors might play a role in the modality-specific peripheral antinociceptive effects of morphine and other clinically relevant mu-opioid agonists. Mechanical nociception was assessed in mice with the paw pressure test (450 g), and heat nociception with the unilateral hot plate (55 degrees C) test. Local peripheral (intraplantar) administration of morphine, buprenorphine or oxycodone did not induce antinociception to mechanical stimulation but had dose-dependent antinociceptive effects on heat stimuli. Local sigma-1 antagonism unmasked peripheral antinociception by mu-opioid agonists to mechanical stimuli, but did not modify their effects on heat stimulation. TRPV1+ and IB4+ cells are segregated populations of small neurons in the dorsal root ganglia (DRG) and the density of sigma-1 receptors was higher in IB4+ cells than in the rest of small nociceptive neurons. The in vivo ablation of TRPV1-expressing neurons with resiniferatoxin did not alter IB4+ neurons in the DRG, mechanical nociception, or the effects of sigma-1 antagonism on local morphine antinociception in this type of stimulus. However, it impaired the responses to heat stimuli and the effect of local morphine on heat nociception. In conclusion, peripheral opioid antinociception to mechanical stimuli is limited by sigma-1 tonic inhibitory actions, whereas peripheral opioid antinociception to heat stimuli (produced in TRPV1-expressing neurons) is not. Therefore, sigma-1 receptors contribute to the modality-specific peripheral effects of opioid analgesics. (C) 2018 The Authors. Published by Elsevier Ltd.

【 授权许可】

Free