ECB-ART-37439
J Tongji Med Univ
1998 Jan 01;184:230-2. doi: 10.1007/bf02886479.
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Effect of SJAMP on human platelet cytoplasmic Ca2+.
Abstract
Using the method of dual-wavelength measurement of platelet [Ca2+]i and Fura-2 as the Ca2+ fluorophore probe, we measured the effect of acidic Mucopolysaccharide from Sticopus Japonicus Selenka (SJAMP) on platelet [Ca2+]i. The results showed that the most significant increase in platelets [Ca2+]i was seen when the concentration of SJAMP was 100 micrograms/ml and the elevation of normal platelet [Ca2+]i was 93.96 +/- 10.24 nmol/L (n = 10). In the presence of extracellular Ca2+ (1 mmol/L), the magnitude of platelet [Ca2+]i response to SJAMP was increased and the [Ca2+]i could reach 116.72 +/- 10.66 nmol/L (n = 10). On the other hand, the magnitude of increased platelet [Ca2+]i induced by SJAMP was smaller and the duration of [Ca2+]i reaching the highest level was longer when compared with other platelet aggregation agents. In the mean time, if platelets were first incubated with cyclooxygenase inhibitor, the rise of [Ca2+]i evoked by SJAMP was inhibited. The results indicated that the mechanism of the rise of [Ca2+]i induced by SJAMP might be dependent upon the generation of prostaglandin endoperoxides and(or) TXA2.
PubMed ID: 10806852
Article link: J Tongji Med Univ
Genes referenced: LOC100893812 srpl
References [+] :
Rink,
Calcium signaling in human platelets.
1990, Pubmed