Mechanisms of the sarcoplasmic reticulum Ca2+ release induced by P2X receptor activation in mesenteric artery myocytes
| Autor: | Maksym I. Harhun, Khrystyna Yu. Sukhanova, V. A. Bouryi, Dmitri V. Gordienko, Oleksandr M. Thugorka |
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| Rok vydání: | 2014 |
| Předmět: |
Male
Agonist medicine.medical_specialty Vascular smooth muscle SERCA Calcium Channels L-Type medicine.drug_class Guinea Pigs Myocytes Smooth Muscle Muscle Smooth Vascular Internal medicine medicine Animals Inositol 1 4 5-Trisphosphate Receptors Myocyte Receptor Mesenteric arteries Pharmacology Muscle Cells Ryanodine receptor Chemistry Cell Membrane Ryanodine Receptor Calcium Release Channel General Medicine musculoskeletal system Mesenteric Arteries Cell biology Sarcoplasmic Reticulum Endocrinology medicine.anatomical_structure Receptors Purinergic P2X cardiovascular system Calcium Ionotropic effect |
| Zdroj: | Pharmacological Reports. 66:363-372 |
| ISSN: | 1734-1140 |
| Popis: | ATP is one of the principal sympathetic neurotransmitters which contracts vascular smooth muscle cells (SMCs) via activation of ionotropic P2X receptors (P2XRs). We have recently demonstrated that contraction of the guinea pig small mesenteric arteries evoked by stimulation of P2XRs is sensitive to inhibitors of IP3 receptors (IP3Rs). Here we analyzed contribution of IP3Rs and ryanodine receptors (RyRs) to [Ca(2+)]i transients induced by P2XR agonist αβ-meATP (10 μM) in single SMCs from these vessels.The effects of inhibition of L-type Ca(2+) channels (VGCCs), RyRs and IP3Rs (5 μM nicardipine, 100 μM tetracaine and 30 μM 2-APB, respectively) on αβ-meATP-induced [Ca(2+)]i transients were analyzed using fast x-y confocal Ca(2+) imaging.The effect of IP3R inhibition on the [Ca(2+)]i transient was significantly stronger (67 ± 7%) than that of RyR inhibition (40 ± 5%) and was attenuated by block of VGCCs. The latter indicates that activation of VGCCs is linked to IP3R-mediated Ca(2+) release. Immunostaining of RyRs and IP3Rs revealed that RyRs are located mainly in deeper sarcoplasmic reticulum (SR) while sub-plasma membrane (PM) SR elements are enriched with type 1 IP3Rs. This structural peculiarity makes IP3Rs more accessible to Ca(2+) entering the cell via VGCCs. Thus, IP3Rs may serve as an "intermediate amplifier" between voltage-gated Ca(2+) entry and RyR-mediated Ca(2+) release.P2X receptor activation in mesenteric artery SMCs recruits IP3Rs-mediated Ca(2+) release from sub-PM SR, which is facilitated by activation of VGCCs. Sensitivity of IP3R-mediated release to VGCC antagonists in vascular SMCs makes this mechanism of special therapeutic significance. |
| Databáze: | OpenAIRE |
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