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Involvement of transglutaminase 2 and voltage-gated potassium channels in cystamine vasodilatation in rat mesenteric small arteries.
Engholm, Morten; Pinilla, Estéfano; Mogensen, Susie; Matchkov, Vladimir; Hedegaard, Elise Røge; Chen, Hua; Mulvany, Michael J; Simonsen, Ulf.
Afiliación
  • Engholm M; Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark.
  • Pinilla E; Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark.
  • Mogensen S; Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark.
  • Matchkov V; Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark.
  • Hedegaard ER; Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark.
  • Chen H; Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark.
  • Mulvany MJ; Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark.
  • Simonsen U; Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark.
Br J Pharmacol ; 173(5): 839-55, 2016 Mar.
Article en En | MEDLINE | ID: mdl-26603619
BACKGROUND AND PURPOSE: Vasodilatation may contribute to the neuroprotective and vascular anti-remodelling effect of the tissue transglutaminase 2 (TG2) inhibitor cystamine. Here, we hypothesized that inhibition of TG2 followed by blockade of smooth muscle calcium entry and/or inhibition of Rho kinase underlies cystamine vasodilatation. EXPERIMENTAL APPROACH: We used rat mesenteric small arteries and RT-PCR, immunoblotting, and measurements of isometric wall tension, intracellular Ca(2+) ([Ca(2+)]i ), K(+) currents (patch clamp), and phosphorylation of myosin phosphatase targeting subunit 1 (MYPT1) and myosin regulatory light chain, in our experiments. KEY RESULTS: RT-PCR and immunoblotting revealed expression of TG2 in mesenteric small arteries. Cystamine concentration-dependently inhibited responses to phenylephrine, 5-HT and U46619 and for extracellular potassium. Selective inhibitors of TG2, LDN 27129 and T101, also inhibited phenylephrine contraction. An inhibitor of PLC suppressed cystamine relaxation. Cystamine relaxed and reduced [Ca(2+)]i in phenylephrine-contracted arteries. In potassium-contracted arteries, cystamine induced less relaxation without changing [Ca(2+)]i , and these relaxations were blocked by mitochondrial complex inhibitors. Blockers of Kv 7 channels, XE991 and linopirdine, inhibited cystamine relaxation and increases in voltage-dependent smooth muscle currents. Cystamine and the Rho kinase inhibitor Y27632 reduced basal MYPT1-Thr(855) phosphorylation, but only Y27632 reduced phenylephrine-induced increases in MYPT1-Thr(855) and myosin regulatory light chain phosphorylation. CONCLUSIONS AND IMPLICATIONS: Cystamine induced vasodilatation by inhibition of receptor-coupled TG2, leading to opening of Kv channels and reduction of intracellular calcium, and by activation of a pathway sensitive to inhibitors of the mitochondrial complexes I and III. Both pathways may contribute to the antihypertensive and neuroprotective effect of cystamine.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Vasodilatación / Transglutaminasas / Cistamina / Canales de Potasio con Entrada de Voltaje / Arterias Mesentéricas Límite: Animals Idioma: En Revista: Br J Pharmacol Año: 2016 Tipo del documento: Article País de afiliación: Dinamarca

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Vasodilatación / Transglutaminasas / Cistamina / Canales de Potasio con Entrada de Voltaje / Arterias Mesentéricas Límite: Animals Idioma: En Revista: Br J Pharmacol Año: 2016 Tipo del documento: Article País de afiliación: Dinamarca