Stimulation of the lateral hypothalamus produces antinociception mediated by 5-HT1A, 5-HT1B and 5-HT3 receptors in the rat spinal cord dorsal horn
- PMID: 16165284
- DOI: 10.1016/j.neuroscience.2005.07.023
Stimulation of the lateral hypothalamus produces antinociception mediated by 5-HT1A, 5-HT1B and 5-HT3 receptors in the rat spinal cord dorsal horn
Abstract
The lateral hypothalamus is part of an efferent system that modifies pain at the spinal cord dorsal horn, but the mechanisms by which lateral hypothalamus-induced antinociception occur are not fully understood. Previous work has shown that antinociception produced from electrical stimulation of the lateral hypothalamus is mediated in part by spinally projecting 5-hydroxytryptamine (5-HT) neurons in the ventromedial medulla. To further examine the role of the lateral hypothalamus in antinociception, the cholinergic agonist carbamylcholine chloride (125 nmol) was microinjected into the lateral hypothalamus of female Sprague-Dawley rats and nociceptive responses measured on the tail-flick and foot-withdrawal tests. Intrathecal injections of the selective 5-HT1A, 5-HT1B, 5-HT3 receptor antagonists, WAY 100135, SB-224289, and tropisetron, respectively, and the non-specific antagonist methysergide, were given. Lateral hypothalamus stimulation with carbamylcholine chloride produced significant antinociception that was blocked by WAY 100135, tropisetron, and SB-224289 on both the tail-flick and foot-withdrawal tests. Methysergide was not different from controls on the tail flick test, but increased foot-withdrawal latencies compared with controls. These results suggest that the lateral hypothalamus modifies nociception in part by activating spinally projecting serotonin neurons that act at 5-HT1A, 5-HT1B, and 5-HT3 receptors in the dorsal horn.
Similar articles
-
Microinjection of carbachol in the lateral hypothalamus produces opposing actions on nociception mediated by alpha(1)- and alpha(2)-adrenoceptors.Brain Res. 2001 Aug 17;911(1):27-36. doi: 10.1016/s0006-8993(01)02567-7. Brain Res. 2001. PMID: 11489441
-
5-hydroxytryptamine 1A (5-HT1A) but not 5-HT3 receptor is involved in mediating the nucleus submedius 5-HT-evoked antinociception in the rat.Brain Res. 2005 Jun 7;1046(1-2):38-44. doi: 10.1016/j.brainres.2005.03.028. Brain Res. 2005. PMID: 15869749
-
5-hydroxytryptamine3 (5-HT3) receptors mediate spinal 5-HT antinociception: an antisense approach.J Pharmacol Exp Ther. 2001 Aug;298(2):674-8. J Pharmacol Exp Ther. 2001. PMID: 11454930
-
Studies on the neuroendocrine role of serotonin.Dan Med Bull. 2007 Nov;54(4):266-88. Dan Med Bull. 2007. PMID: 18208678 Review.
-
5-HT1A and 5-HT1B receptor agonists and aggression: a pharmacological challenge of the serotonin deficiency hypothesis.Eur J Pharmacol. 2005 Dec 5;526(1-3):125-39. doi: 10.1016/j.ejphar.2005.09.065. Epub 2005 Nov 28. Eur J Pharmacol. 2005. PMID: 16310183 Review.
Cited by
-
Lateral hypothalamic-induced antinociception may be mediated by a substance P connection with the rostral ventromedial medulla.Brain Res. 2008 Jun 12;1214:40-9. doi: 10.1016/j.brainres.2008.03.051. Epub 2008 Apr 8. Brain Res. 2008. PMID: 18457815 Free PMC article.
-
Conditioned pain modulation is associated with common polymorphisms in the serotonin transporter gene.PLoS One. 2011 Mar 28;6(3):e18252. doi: 10.1371/journal.pone.0018252. PLoS One. 2011. PMID: 21464942 Free PMC article. Clinical Trial.
-
Efficacy of Desvenlafaxine in Reducing Migraine Frequency and Severity: A Retrospective Study.J Clin Med. 2024 Aug 30;13(17):5156. doi: 10.3390/jcm13175156. J Clin Med. 2024. PMID: 39274369 Free PMC article.
-
Pain Inhibits Pain: an Ascending-Descending Pain Modulation Pathway Linking Mesolimbic and Classical Descending Mechanisms.Mol Neurobiol. 2019 Feb;56(2):1000-1013. doi: 10.1007/s12035-018-1116-7. Epub 2018 Jun 1. Mol Neurobiol. 2019. PMID: 29858776
-
The posterior hypothalamus exerts opposing effects on nociception via the A7 catecholamine cell group in rats.Neuroscience. 2012 Dec 27;227:144-53. doi: 10.1016/j.neuroscience.2012.09.058. Epub 2012 Oct 2. Neuroscience. 2012. PMID: 23036619 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical