Pharmacological characterization of alpha adrenoceptor-mediated motor responses in the rat colon

Background: Inhibitory neuromuscular transmission in the gastrointestinal tract is mediated by intrinsic nitrergic and purinergic neurons. Purines activate G protein-coupled receptor P2Y receptors, increasing intracellular Ca that activates small conductance calcium-activated potassium (SK) channels...

Descripción completa

Detalles Bibliográficos
Autores: Traserra, Sara, Grao, Marc, Trujillo, Sonia, Jiménez Altayó, Francesc|||0000-0002-9034-2041, Vergara, Patri|||0000-0002-9220-6406, Jiménez Farrerons, Marcel|||0000-0002-6602-7332
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:302960
Acceso en línea:https://ddd.uab.cat/record/302960
https://dx.doi.org/urn:doi:10.1111/nmo.14921
Access Level:acceso abierto
Palabra clave:Alpha adrenoceptors
Apamin
Colon
Phenylephrine
Relaxation
Descripción
Sumario:Background: Inhibitory neuromuscular transmission in the gastrointestinal tract is mediated by intrinsic nitrergic and purinergic neurons. Purines activate G protein-coupled receptor P2Y receptors, increasing intracellular Ca that activates small conductance calcium-activated potassium (SK) channels. Little is known about the effect of adrenergic receptor activation on intestinal smooth muscle. In vascular tissue, stimulation of α-adrenoceptors causes smooth muscle contraction, while their effect on intestinal tissue is poorly understood. This study aimed to pharmacologically characterize the effect of α-adrenoceptor activation in the rat colon, which shares similar inhibitory pathways to the human colon. Methods: Muscle bath experiments were performed with the rat proximal, mid, and distal colon oriented both circularly and longitudinally. Results: The α-adrenoceptor agonist phenylephrine (PE) (10-10 M) evoked concentration-dependent relaxations of the intestinal smooth muscle from all regions and orientations. However, in the mid-circular colon at low PE concentrations, a contraction sensitive to 10 M phentolamine (non-selective α-adrenoceptor blocker), the neural blocker tetrodotoxin (TTX; 10 M), and atropine (10 M) was recorded. PE-induced relaxations were insensitive to TTX (10 M) and the nonselective β-adrenoceptor blocker propranolol (10 M). In contrast, PE-induced relaxations were blocked by phentolamine (10 M), prazosin (10 M) (α-adrenoceptor blocker), and RS17053 (10 M) (α-blocker), but not by yohimbine (10 M) (α-adrenoceptor blocker). Apamin (10 M), a SK channel blocker, abolished PE-induced relaxations. Conclusions: Contractile responses in the circular muscle of the mid colon could be attributed to α-adrenoceptors located on enteric cholinergic neurons. Stimulation of α-adrenoreceptors activates SK channels to cause smooth muscle relaxation, which constitutes a signaling pathway that shares similarities with P2Y receptors.