HE Huan, ZHANG Shuo, ZHANG Min, et al. Douchi Fibrinolytic Kinase DCK Thrombolysis and Antithrombotic Function [J]. Chinese journal of experimental traditional medical formulae, 2016, 22(14): 135-138.
DOI:
HE Huan, ZHANG Shuo, ZHANG Min, et al. Douchi Fibrinolytic Kinase DCK Thrombolysis and Antithrombotic Function [J]. Chinese journal of experimental traditional medical formulae, 2016, 22(14): 135-138. DOI: 10.13422/j.cnki.syfjx.2016140135.
Douchi Fibrinolytic Kinase DCK Thrombolysis and Antithrombotic Function
Objective: To study Guizhou Douchi fibrinolytic kinase DCK(DCK enzyme)thrombolysis and antithrombotic function in vivo. Method: Male Kunming mice were randomly divided into model group
urokinase control group(150 U · g-1)
DCK enzyme low
medium and high dose group (150
300
450 U · g-1)
ip 7 d
once a day
each group were injected 0.8% carrageenan to build the thrombus model in tail after 30 minutes 7 days administration. Tail thrombosis was observed and the mice tail length and the length of thrombus were measured at 24
36 h. Thrombus formation rate and thrombosis relative length were calculated. Wistar rats were randomly divided into model group
urokinase control group(100 U · g-1)and DCK enzyme low
medium and high dose group(100
200
300 U · g-1)
ip 10 days
once a day. Rats were anesthetized by chloral hydrate solution after 30 minutes the 10 days treatment
the right common carotid artery and left external jugular vein were separated to build the right common carotid artery-left external jugular vein bypass. Thrombus wet weight were get in the bypass circulation. New Zealand white rabbits were randomly divided into model group
urokinase control group (38 U · g-1)
DCK enzyme low
medium and high dose group (38
76
114 U · g-1)by ear vein injection administration
blood sampling of ear border vein were administered after 1 h to detect prothrombin time(PT)
activated partial thromboplastin time(APTT)
thrombin time(TT)
human fibrinogen(FIB)
euglobulin clot lysis time(ELT)and fibrin(-ogen)degradation products(FDP). Result: Compared with the model group
DCK enzyme group at 24
36 h tail thrombosis formation relative length were reduced(P<0.01
P<0.05)
DCK enzyme of high
middle dose group of bypass thrombus wet weight were reduced(P<0.01
P< 0.05). The PT
APTT
TT time extended with significant difference (P<0.01
P< 0.05)
the FIB of high DCK enzyme group was reduced (P<0.05
P<0.01)
high DCK enzyme and middle dose group of ELT was decreased(P< 0.05)
and DCK enzyme in each experimental group FDP content were increased
the middle dose group increased(P<0.05). Conclusion: DCK enzyme has a certain thrombolysis and antithrombotic function in vivo.
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