T-type calcium channels contribute to colonic hypersensitivity in a rat model of irritable bowel syndrome

التفاصيل البيبلوغرافية
العنوان: T-type calcium channels contribute to colonic hypersensitivity in a rat model of irritable bowel syndrome
المؤلفون: Juan F. Sanguesa Ferrer, Emilie Muller, Fabrice Marger, Abdelkrim Alloui, Terrance P. Snutch, Joël Nargeot, Emmanuel Bourinet, Julien Matricon, Denis Ardid, Christian Barrère, Anne Pizzoccaro, Alain Eschalier, Agathe Gelot
المصدر: Proceedings of the National Academy of Sciences. 108:11268-11273
بيانات النشر: Proceedings of the National Academy of Sciences, 2011.
سنة النشر: 2011
مصطلحات موضوعية: Male, Abdominal pain, Colon, Pharmacology, Irritable Bowel Syndrome, Rats, Sprague-Dawley, Calcium Channels, T-Type, medicine, Animals, RNA, Small Interfering, Irritable bowel syndrome, Multidisciplinary, Base Sequence, Voltage-dependent calcium channel, business.industry, Calcium channel, T-type calcium channel, Nociceptors, Pain Perception, Visceral pain, Biological Sciences, Calcium Channel Blockers, medicine.disease, Electrophysiological Phenomena, Rats, Butyrates, Disease Models, Animal, Gene Knockdown Techniques, Anesthesia, Neuropathic pain, Nociceptor, Neuralgia, medicine.symptom, business
الوصف: The symptoms of irritable bowel syndrome (IBS) include significant abdominal pain and bloating. Current treatments are empirical and often poorly efficacious, and there is a need for the development of new and efficient analgesics aimed at IBS patients. T-type calcium channels have previously been validated as a potential target to treat certain neuropathic pain pathologies. Here we report that T-type calcium channels encoded by the Ca V 3.2 isoform are expressed in colonic nociceptive primary afferent neurons and that they contribute to the exaggerated pain perception in a butyrate-mediated rodent model of IBS. Both the selective genetic inhibition of Ca V 3.2 channels and pharmacological blockade with calcium channel antagonists attenuates IBS-like painful symptoms. Mechanistically, butyrate acts to promote the increased insertion of Ca V 3.2 channels into primary sensory neuron membranes, likely via a posttranslational effect. The butyrate-mediated regulation can be recapitulated with recombinant Ca V 3.2 channels expressed in HEK cells and may provide a convenient in vitro screening system for the identification of T-type channel blockers relevant to visceral pain. These results implicate T-type calcium channels in the pathophysiology of chronic visceral pain and suggest Ca V 3.2 as a promising target for the development of efficient analgesics for the visceral discomfort and pain associated with IBS.
تدمد: 1091-6490
0027-8424
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3d0e9b654c3923485d0f0686f5e841aTest
https://doi.org/10.1073/pnas.1100869108Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....d3d0e9b654c3923485d0f0686f5e841a
قاعدة البيانات: OpenAIRE