Key result
Extracellular ATP (>0.1 mM) induced a concentration-dependent increase in intracellular chloride and transient acidification in isolated guinea pig ventricular muscles.
Why the study?
Does extracellular ATP increase intracellular chloride concentration in isolated guinea pig ventricular muscles?
Does extracellular ATP increase intracellular chloride concentration in isolated guinea pig ventricular muscles?
Extracellular ATP increases intracellular chloride concentration in guinea pig ventricular muscles, suggesting a mechanism for ischemia-induced chloride accumulation.
Guinea pig data are hypothesis-generating; leaves open relevance to human ischemia or arrhythmias.
We investigated effects of extracellular ATP on intracellular chloride activities ([Cl-]i) and possible contribution of the Cl--HCO3- exchange to this increase in [Cl-]i in isolated guinea pig ventricular muscles. The [Cl-]i and intracellular pH (pHi) were recorded in quiescent ventricular muscles using double-barreled ion-selective microelectrode techniques. MgATP at a concentration higher than 0.1 mM, induced an increase in [Cl-]i, and this increase in [Cl-]i was dependent on the concentration of ATP but not on the concentration of magnesium ions present in the perfusion solution. NaADP, but not NaAMP, at a concentration of 0.5 mM induced a similar increase in [Cl-]i as that induced by MgATP. However, the NaADP-induced increase in [Cl-]i was transient and gradually returned to the control level even though NaADP was continuously present. Furthermore, ATP also triggered a transient acidification of pHi, and both increases in [Cl-]i and intracellular H+ induced by ATP were prevented when preparations were pretreated with stilbene derivatives, SITS and DIDS, or perfused with a Cl--free solution. Our findings showed that the increased extracellular ATP concentrations might trigger an increase in [Cl-]i in ventricular muscles. In light of previous studies showing that cardiac ischemia induced increases in extracellular nucleotide concentrations and [Cl-]i in ventricular muscles, we propose that ischemia-induced accumulation of ATP concentration in the extracellular space may be an important factor to trigger increment of [Cl-]i during ischemic conditions.
No takes yet. Share an insight, caveat, or question.
Lai et al. (2000) studied Isolated guinea pig ventricular muscles. Extracellular ATP was evaluated on Intracellular chloride activities ([Cl-]i) and intracellular pH (pHi). Extracellular ATP (>0.1 mM) induced a concentration-dependent increase in intracellular chloride and transient acidification in isolated guinea pig ventricular muscles.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: