TY - JOUR
T1 - Elevation of intracellular Ca2+ concentration in rabbit nonpigmented ciliary epithelial cells by allicin
AU - Chu, Teh Ching
AU - Burch, Jarrett L.
AU - De Paula Brotto, Marco A.
AU - Creazzo, Tony L.
AU - Han, Joan
AU - Han, Grace Y.
AU - Potter, David E.
N1 - Funding Information:
This work was supported, in part, by NIH Grants EY 06338 (DEP) , S06GM 45199 (GYH) and HL 36059 (TLC). Rabbit non&ymmted ciliary epithelialc ells were generouslyp rovided by Dr. M. Coca&ados, Yale University.
PY - 1996/9
Y1 - 1996/9
N2 - A previous study has shown that allicin produces changes in aqueous humor dynamics, and this study was conducted to examine possible cellular mechanisms. In rabbit nonpigmented ciliary epithelial cells, basal levels of [Ca2+](i) were determined to be 164 ± 34 nM. Allicin, a sulfhydryl-reactive agent, induced Ca2+ transients at 0.01 mM and at 0.2 mM, the Ca2+ transient peaked at 732 ± 33 nM. Allicin-induced Ca2+ transients were prevented by pretreatment with dithiothreitol which did not affect the basal Ca2+ levels. Allicin had only a slight, insignificant, effect on L-type Ca2+ currents, and allicin-induced Ca2+ transients were also present under extracellular Ca2+-free conditions. These data suggest that intracellular Ca2+ stores are the most probable source of allicin's effect. Pretreatment of cells with ryanodine, an inhibitor of Ca2+-induced-Ca2+-release, inhibited allicin-induced Ca2+ transients, but the basal Ca2+ levels were unaffected by ryanodine. Thus, allicin-induced Ca2+ transients are most likely mediated through ryanodine-sensitive intracellular Ca2+ stores. Copyright (C) 1996 Elsevier Science Inc.
AB - A previous study has shown that allicin produces changes in aqueous humor dynamics, and this study was conducted to examine possible cellular mechanisms. In rabbit nonpigmented ciliary epithelial cells, basal levels of [Ca2+](i) were determined to be 164 ± 34 nM. Allicin, a sulfhydryl-reactive agent, induced Ca2+ transients at 0.01 mM and at 0.2 mM, the Ca2+ transient peaked at 732 ± 33 nM. Allicin-induced Ca2+ transients were prevented by pretreatment with dithiothreitol which did not affect the basal Ca2+ levels. Allicin had only a slight, insignificant, effect on L-type Ca2+ currents, and allicin-induced Ca2+ transients were also present under extracellular Ca2+-free conditions. These data suggest that intracellular Ca2+ stores are the most probable source of allicin's effect. Pretreatment of cells with ryanodine, an inhibitor of Ca2+-induced-Ca2+-release, inhibited allicin-induced Ca2+ transients, but the basal Ca2+ levels were unaffected by ryanodine. Thus, allicin-induced Ca2+ transients are most likely mediated through ryanodine-sensitive intracellular Ca2+ stores. Copyright (C) 1996 Elsevier Science Inc.
KW - Ca current
KW - Ca-induced-Ca-release
KW - allicin
KW - intracellular Ca concentration
KW - nonpigmented ciliary epithelial cells
KW - rabbit
KW - ryanodine
KW - sulfhydryl group
UR - http://www.scopus.com/inward/record.url?scp=0030222486&partnerID=8YFLogxK
U2 - 10.1016/S0742-8413(96)00115-6
DO - 10.1016/S0742-8413(96)00115-6
M3 - Article
C2 - 8983172
AN - SCOPUS:0030222486
SN - 0742-8413
VL - 115
SP - 89
EP - 94
JO - Comparative Biochemistry and Physiology - C Pharmacology Toxicology and Endocrinology
JF - Comparative Biochemistry and Physiology - C Pharmacology Toxicology and Endocrinology
IS - 1
ER -