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. 2000 Jul 15;526(Pt 2):313–326. doi: 10.1111/j.1469-7793.2000.00313.x

Figure 5. Analyses of VDCC subtypes contributing to CHA-induced ICa inhibition.

Figure 5

A, a representative experiment illustrating the effect of 106 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 (106 M; GVIA). P/Q -type Ca2+ current was the component irreversibly blocked by a combination of ω-Aga-IVA (107 M; AgaIVA) and ω-CTx-MVIIC (106 M; MVIIC). L-type Ca2+ current was the component reversibly blocked by nifedipine (105 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 106 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.