TY - JOUR
T1 - Antihaemostatic and antithrombotic effect of some antiplatelet agents isolated from Chinese herbs
AU - TENG, CHE‐MING ‐M
AU - KO, FENG‐NIEN ‐N
AU - WANG, JIH‐PYANG ‐P
AU - LIN, CHUN‐NAN ‐N
AU - Wu, Tian-Shung
AU - CHEN, CHIEN‐CHIH ‐C
AU - HUANG, TUR‐FU ‐F
PY - 1991/1/1
Y1 - 1991/1/1
N2 - Abstract— Five antiplatelet agents have been isolated from Chinese herbs. Apigenin and magnolol are inhibitors of thromboxane synthesis, while osthole, protopine and norathyriol are inhibitors of phosphoinositide breakdown. Thirty min after intraperitoneal (i.p.) administration of these drugs, tail bleeding time of mice was prolonged markedly in a dose‐dependent manner by norathyriol, protopine, osthole and magnolol, but not by apigenin. However, the antiplatelet agents (up to 200 mg kg−1, i.p.) could not prevent acute thromboembolic death in mice. In endotoxin‐induced experimental disseminated intravascular coagulation in rats, norathyriol (50–100 mg kg−1, i.p.) prevented the decrease in platelet counts and fibrinogen, and the prolongation of plasma prothrombin time. Norathyriol (100 mg kg−1, i.p.) also suppressed ex‐vivo platelet aggregation induced by collagen and ADP in rat plasma. 1991 Royal Pharmaceutical Society of Great Britain
AB - Abstract— Five antiplatelet agents have been isolated from Chinese herbs. Apigenin and magnolol are inhibitors of thromboxane synthesis, while osthole, protopine and norathyriol are inhibitors of phosphoinositide breakdown. Thirty min after intraperitoneal (i.p.) administration of these drugs, tail bleeding time of mice was prolonged markedly in a dose‐dependent manner by norathyriol, protopine, osthole and magnolol, but not by apigenin. However, the antiplatelet agents (up to 200 mg kg−1, i.p.) could not prevent acute thromboembolic death in mice. In endotoxin‐induced experimental disseminated intravascular coagulation in rats, norathyriol (50–100 mg kg−1, i.p.) prevented the decrease in platelet counts and fibrinogen, and the prolongation of plasma prothrombin time. Norathyriol (100 mg kg−1, i.p.) also suppressed ex‐vivo platelet aggregation induced by collagen and ADP in rat plasma. 1991 Royal Pharmaceutical Society of Great Britain
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U2 - 10.1111/j.2042-7158.1991.tb03561.x
DO - 10.1111/j.2042-7158.1991.tb03561.x
M3 - Article
C2 - 1685529
AN - SCOPUS:0025894809
VL - 43
SP - 667
EP - 669
JO - Journal of Pharmacy and Pharmacology
JF - Journal of Pharmacy and Pharmacology
SN - 0022-3573
IS - 9
ER -