Publication | Open Access
Measurement of chloride flux associated with the myogenic response in rat cerebral arteries
45
Citations
33
References
2001
Year
HypertensionCardiovascular PharmacologyPharmacotherapyRat Cerebral ArteriesSocial SciencesBlood FlowCerebral Vascular RegulationMicrom TamoxifenNeurologyVascular PharmacologyMyogenic ResponseIon ChannelsVascular BiologyNervous SystemCerebral Blood FlowPharmacologyChloride FluxNeurophysiologyPhysiologyElectrophysiologyNeuroscienceCentral Nervous SystemMyogenic ToneMedicineMyogenic Contraction
1. Self-referencing ion-selective (SERIS) electrodes were used to measure the temperature and pressure dependence of Cl(-) efflux, during myogenic contraction of pressurized rat cerebral resistance arteries. 2. At room temperature (18-21 degrees C), a small, pressure-independent Cl(-) efflux was measured. On warming to 37 degrees C, arteries developed pressure-dependent myogenic tone, and this was associated with a pressure-dependent increase in Cl(-) efflux (n = 5). 3. Both myogenic tone and the pressure- and temperature-dependent Cl(-) efflux were abolished on application of 10 microM tamoxifen, a Cl(-) channel blocker (IC(50) 3.75 +/- 0.2 microM). Tamoxifen (10 microM) also prevented contraction to 60 mM K(+), suggesting non-specific effects of tamoxifen (n = 5). 4. Myogenic tone was abolished by 2 microM nimodipine, but Cl(-) efflux was unaffected. In the presence of nimodipine, 10 microM tamoxifen still abolished pressure- and temperature-dependent Cl(-) efflux (n = 3). 5. In summary, a Cl(-) efflux can be measured from rat cerebral arteries, with a temperature dependence that is closely correlated with myogenic contraction. We conclude that Cl(-) efflux through Cl(-) channels contributes to the depolarization associated with myogenic contraction.
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