Synergism between toxin-γ from Brazilian scorpion Tityus serrulatus and veratridine in chromaffin cells
0301 basic medicine
sodium current
570
Veratridine
Calcium Radioisotopes
Neurotoxins
Electric Conductivity
Scorpion Venoms
Drug Synergism
calcium uptake
Calcium Channel Blockers
Sodium Channels
oscillations of cytosolic calcium
Kinetics
Norepinephrine
03 medical and health sciences
Adrenal Medulla
catecholamine release
Chromaffin System
Animals
Calcium
Cattle
Calcium Channels
DOI:
10.1152/ajpcell.1998.274.6.c1745
Publication Date:
2017-12-24T17:25:49Z
AUTHORS (9)
ABSTRACT
Toxin-γ (Tγ) from the Brazilian scorpion Tityus serrulatus venom caused a concentration- and time-dependent increase in the release of norepinephrine and epinephrine from bovine adrenal medullary chromaffin cells. Tγ was ∼200-fold more potent than veratridine judged from EC50 values, although the maximal secretory efficacy of veratridine was 10-fold greater than that of Tγ (1.2 vs. 12 μg/ml of catecholamine release). The combination of both toxins produced a synergistic effect that was particularly drastic at 5 mM extracellular Ca2+concentration ([Ca2+]o), when 30 μM veratridine plus 0.45 μM Tγ were used. Tγ (0.45 μM) doubled the basal uptake of45Ca2+, whereas veratridine (100 μM) tripled it. Again, a drastic synergism in enhancing Ca2+ entry was seen when Tγ and veratridine were combined; this was particularly pronounced at 5 mM [Ca2+]o. Veratridine induced oscillations of cytosolic Ca2+ concentration ([Ca2+]i) in single fura 2-loaded cells without elevation of basal levels. In contrast, Tγ elevated basal [Ca2+]ilevels, causing only small oscillations. When added together, Tγ and veratridine elevated the basal levels of [Ca2+]iwithout causing large oscillations. Tγ shifted the current-voltage ( I-V) curve for Na+ channel current to the left. The combination of Tγ with veratridine increased the shift of the I-V curve to the left, resulting in a greater recruitment of Na+channels at more hyperpolarizing potentials. This led to enhanced and more rapid accumulation of Na+ in the cell, causing cell depolarization, the opening of voltage-dependent Ca2+ channels, and Ca2+ entry and secretion.
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