1.Qualities of Whitmania pigra in different-month-age and best harvest time.
Hongzhuan SHI ; Qiaosheng GUO ; Shusong LU ; Hui LI
China Journal of Chinese Materia Medica 2009;34(23):3060-3063
OBJECTIVEDynamic changes of quality and growth of Whitmania pigra were investigated to provide theoretical basis for quality control and determination of optimal harvest time.
METHODThe contents of moisture, ethanol-soluble extractive, total ash, and acid-insoluble ash, as well as antithrombin activity were determined according to Chinese pharmacopoeia (2005 edition).
RESULTQualities of W. pigra collected from different growth stages met the standards of Chinese pharmacopoeia (2005 edition). The highest amount of ethanol-soluble extract was found in 9-month-old, W. pigra, followed by 6-month-aged ones. And there was significant difference between 9-month-old and 4-month-old, 7 month-old and 11 month-old (P < 0.05). The highest antithrombin activity was detected in 6 month-old W. pigra, followed by 10 month-old. Significant differences of antithrombin activity were found between 6-month-old and 4 month-old ones, and 5 month-old (P < 0.05), however, there were no significant difference between 6 month-old ones with other samples. Eleven-month-old W. pigra got the most dry weight, and there were significant difference between 11 month-old ones with other samples (P < 0.05).
CONCLUSIONNovember, namely for 6 month old artificial cultivated W. pigra was the best harvest time in Jiangsu and Zhejiang provinces.
Animals ; Antithrombin III ; Antithrombins ; analysis ; China ; Leeches ; chemistry ; growth & development ; Medicine, Chinese Traditional ; Peptide Fragments
2.Study on antiplatelet and antithrombin activitives and effective components variation of Puhuang-Wulingzhi before and after compatibility.
Shu-lan SU ; Ping XUE ; Zhen OUYANG ; Wei ZHOU ; Jin-ao DUAN
China Journal of Chinese Materia Medica 2015;40(16):3187-3193
The changes of bioactive constituents were analyzed for Puhuang-Wulingzhi before and after compatibility and the antiplatelet and antithrombin activitives were evaluated in order to elucidate the scientific and reasonable of Puhuang-Wulingzhi compatibility. UPLC-QTOF-MA-Markerlynx, principal component analysis (PCA) and orthogonal partial least-squares discriminant analysis were used for data analysis and tracking changes of chemical composition during the decocting process. In vitro platelet aggregation induced by ADP, thrombin time(TT) and prothrombin time (PT) were investigated for Puhuang-Wulingzhi before and after compatibility. The results showed that significant differences were found between the mixed decoction and codecoction of Wulingzhi and Puhuang. Five compounds changed obviously were identified as typhaneoside, naringenin, isorhamnetin-3-O-ruinoside, quercetin-3-O-neohesperidoside, kaempferol-3-O-neohesperidoside. The codecoction, comparing with the single decoction, was more significant in antiplatelet aggregation and could prolong thrombin time. In the same crude drug dose, the thrombin time (TT) elongation were greater. These data could provide references for elucidation of bioactive components for this herb pair.
Animals
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Antithrombins
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chemistry
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pharmacology
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Blood Platelets
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drug effects
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physiology
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Drugs, Chinese Herbal
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chemistry
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pharmacology
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Female
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Humans
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Molecular Structure
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Platelet Aggregation
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drug effects
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Rabbits
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Thrombin Time
3.Type I antithrombin deficiency due to 13389G deletion in antithrombin gene.
Qihua FU ; Xianguo XU ; Qiulan DING ; Yiqun HU ; Xuefeng WANG ; Hongli WANG
Chinese Journal of Hematology 2002;23(11):588-590
OBJECTIVETo identify the gene mutation of a kindred with type I antithrombin deficiency.
METHODSAll of the seven exons and intron-exon boundaries of antithrombin gene were analysed by PCR and direct sequencing of amplified PCR products from the propositus.
RESULTSA 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.
CONCLUSIONThis is a novel mutation, which can cause antithrombin deficiency and thrombosis.
Adolescent ; Antithrombins ; deficiency ; genetics ; Base Sequence ; DNA ; chemistry ; genetics ; DNA Mutational Analysis ; Family Health ; Frameshift Mutation ; Humans ; Male ; Pedigree ; Sequence Deletion
4.Plasma Level of IL-6 and Its Relationship to Procoagulant and Fibrinolytic Markers in Acute Ischemic Stroke.
Jae Woo SONG ; Kyung Soon SONG ; Jong Rak CHOI ; Shin Young KIM ; Ji Hyuk RHEE
Yonsei Medical Journal 2006;47(2):201-206
Procoagulant or impaired fibrinolytic states as well as inflammatory reactions mediated by cytokines are likely involved in the pathogenesis of acute ischemic stroke. We examined the potential relationship between interleukin 6 (IL-6) and hemostatic markers. The procoagulant and fibrinolytic states were assessed in 46 patients with acute stroke by measuring plasma levels of plasminogen activator inhibitor-1 (PAI-1), thrombin-antithrombin complex (TAT), and plasminogen-antiplasmin complex (PAP). Circulating IL-6 levels were measured using ELISA (Quantikine, R and D systems, MN, USA). Circulating IL-6 (mean, 26.5 pg/mL) and PAI-1 (mean, 19.9 ng/mL) levels were higher in patients with acute stroke than in healthy subjects (mean, 3.0 pg/mL, 10.4 ng/mL, respectively). TAT levels were statistically different according to the etiologic subtypes of stroke (atherogenic, 2.5 ng/mL; lacunar 3.2 ng/mL; cardiogenic 9.9 ng/mL, p = 0.021). Neither procoagulant levels nor fibrinolytic markers significantly correlated with circulating IL-6 levels. Our findings suggest that elevated proinflammatory cytokines during the initial hours of ischemic stroke may be an independent pathogenic factor or a consequence of the thrombotic event with no relationship to the procoagulant or fibrinolytic states.
Thrombosis
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Thrombolytic Therapy
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Thrombin/chemistry
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Plasminogen Activator Inhibitor 1/blood
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Phospholipids/chemistry
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Models, Statistical
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Middle Aged
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Male
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Ischemia/*blood/*pathology
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Interleukin-6/*blood/metabolism
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Humans
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Hemostasis
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*Fibrinolysis
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Female
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Enzyme-Linked Immunosorbent Assay
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Cytokines/metabolism
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Coagulants/*metabolism
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Cerebrovascular Accident/*blood/*pathology
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Blood Coagulation Factors/metabolism
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Antithrombins/chemistry
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Aged
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Acute Disease