Figure 5. Analyses of VDCC subtypes contributing to CHA-induced ICa inhibition.
A, a representative experiment illustrating the effect of 10−6 M CHA on ICa before and after application of various selective Ca2+ channel blockers. N-type Ca2+ current was the component irreversibly blocked by ω-CTx-GVIA (10−6 M; GVIA). P/Q -type Ca2+ current was the component irreversibly blocked by a combination of ω-Aga-IVA (10−7 M; AgaIVA) and ω-CTx-MVIIC (10−6 M; MVIIC). L-type Ca2+ current was the component reversibly blocked by nifedipine (10−5 M). The residual component insensitive to these drugs was regarded as R-type. B, summary of the distribution of high-voltage-activated Ca2+ channel subtypes (outer circle) and their fractional components which were sensitive to 10−6 M CHA (inner circle, black area) from four SON neurones. C, summary data for the relative proportion of each Ca2+ channel subtype that contributed to the total CHA-induced ICa inhibition.