6533b873fe1ef96bd12d577c

RESEARCH PRODUCT

Effects of phorbol 12,13-diacetate on human isolated bronchus

Esteban J. MorcilloBenjamín SarriáJulio CortijoGenaro GalanConsuelo Pedrós

subject

Cromakalimmedicine.medical_specialtyBronchiIn Vitro TechniquesOuabainPotassium ChlorideContractilityCalcium Chloridechemistry.chemical_compoundTheophyllineInternal medicinePhorbol EstersmedicineExtracellularHumansStaurosporineOuabainEgtazic AcidProtein Kinase CProtein kinase CPharmacologyDose-Response Relationship DrugChemistryEndocrinologyCalphostin CPhorbolBiophysicsmedicine.symptommedicine.drugMuscle contraction

description

Protein kinase C appears to be involved in the regulation of airway contractility. Phorbol 12,13-diacetate (PDA; 0.01-10 microM), a protein kinase C activator, produced a transient relaxation followed by a sustained contraction of human isolated bronchus. Different protein kinase C inhibitors (calphostin C, staurosporine and 1-(5-isoquinolinesulfonyl)-2-methylpiperazine) (H-7), nifedipine (NIF; 1 microM) or incubation with Ca(2+)-free medium, inhibited the spasmogenic response to phorbol, while ouabain (10 microM) suppressed only the initial relaxation. These results indicate that the initial relaxation, in response to PDA, is related to the activation of Na(+)/K(+)-ATPase, while the ensuing contraction depends on extracellular Ca(2+) entry.Incubation with PDA (1-5 microM) depressed the maximal relaxation to theophylline and caffeine obtained at 37 degrees C but augmented the spasmogenic responses to methylxanthines (10 mM) obtained in cooled preparations. These effects do not result apparently from increased extracellular entry of Ca(2+), but instead, from facilitation of the release of Ca(2+) from intracellular stores.

https://doi.org/10.1016/s0014-2999(00)00351-4