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Blockade of 5-HT7 receptors reduces tactile allodynia in the rat

This study assessed the role of systemic and spinal 5-HT(7) receptors on rats submitted to spinal nerve injury. In addition, the 5-HT(7) receptors level in dorsal root ganglion and spinal cord was also determined. Tactile allodynia was induced by L5/L6 spinal nerve ligation. Systemic (0.01-10mg/kg) or spinal (0.3-30 mug) administration of the selective 5-HT(7) receptor antagonist SB-269970 but not vehicle reduced in a dose-dependent manner established tactile allodynia. This effect was maintained for about 6h. SB-269970 was more potent and effective by the spinal administration route than through systemic injection. Spinal nerve ligation reduced expression of 5-HT(7) receptors in the ipsilateral but not contralateral dorsal root ganglia. Moreover, 5-HT(7) receptor levels were lower in the ipsilateral dorsal spinal cord of neuropathic rats compared to naive and sham rats. No changes in the receptor levels were observed in the contralateral dorsal spinal cord and in both regions of the ventral spinal cord. Data suggest that spinal 5-HT(7) receptors play a pronociceptive role in neuropathic rats. Results also indicate that spinal nerve injury leads to a reduced 5-HT(7) receptors level in pain processing-related areas which may result from its nociceptive role in this model. Data suggest that selective 5-HT(7) receptor antagonists may function as analgesics in nerve injury pain states

Keywords : Analgesics,Animals,Area Under Curve,Blotting,Western,Data Interpretation,Statistical,drug effects,drug therapy,Female,Functional Laterality,Hyperalgesia,Injections,Intraperitoneal,Injections,Spinal,injuries,Ligation,metabolism,Neuralgia,Pain,Pain Measurement,pharmacology,Phenols,Physical Stimulation,physiology,Posterior Horn Cells,psychology,Rats,Rats,Wistar,Receptors,Serotonin,Serotonin Antagonists,Spinal Cord,Spinal Nerves,Sulfonamides,, 5ht(7),Receptors,Reduces,Tactile, nerve injections in back

Date of Publication : 2011 Oct

Authors : maya-Castellanos E;Pineda-Farias JB;Castaneda-Corral G;Vidal-Cantu GC;Murbartian J;Rocha-Gonzalez HI;Granados-Soto V;

Organisation : Departamento de Farmacobiologia, Centro de Investigacion y de Estudios Avanzados (Cinvestav), Sede Sur, Mexico, D.F., Mexico

Journal of Publication : Pharmacol Biochem Behav

Pubmed Link : https://www.ncbi.nlm.nih.gov/pubmed/21693130

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