• 제목/요약/키워드: anticoagulant activities

Search Result 67, Processing Time 0.034 seconds

Effect of porcine testis-derived glycosaminoglycans on blood coagulation and immune responses

  • Yoo, Yung-Choon;Lee, Kyung-Box
    • 대한약학회:학술대회논문집
    • /
    • 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
    • /
    • pp.327.1-327.1
    • /
    • 2002
  • Glycosaminoglycans(PT -Gag) were isolated from the porcine testis. From the PT -Gag, we obtained two different types of Gag fractions using Dowex macro porous Resin MSA-1 column, PT -Gag-1.5% NaCl and PT -Gag-16% NaCl. Various biological activities of the GAGs were examined in aspect of anticoagulant and immunomodulating activity. The anticoagulant activity of the GAGs was evaluated by activated partial thromboplastin time (aPTT ) assay and thrombin time (TT) assay. The GAGs of porcine testis markedly incresed the clotting times of both of aPTT and TT. showing that PT-Gag-16% NaCl was more effective than PT-Gag-1.5% NaCl. The immunomodulating activityof the GAGs was examined in relation to regulation of xytoxine prodution of murine peritoeal maerophages. Taken together. GAGs isolated from porcine testis possess bilolgical functions such as anticoagulant and immunomodulating activity.

  • PDF

Effect of oral administration of Ginsenoside-Rb2 on rotavirus infection

  • Yoo, Yung-Choon;Lee, Kyung-Bok
    • 대한약학회:학술대회논문집
    • /
    • 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
    • /
    • pp.276.2-276.2
    • /
    • 2002
  • Glycosaminoglycans(PT -Gag) were isolated from the porcine testis. From the PT -Gag. we obtained two different types of Gag fractions using Dowex macroporous Resin MSA-1 column. PT-Gag-1.5% NaCl and PT -Gag-16% NaCl. Various biological activities of the GAGs were examined in aspect of anticoagulant and immunomodulating activity. The anticoagulant activity of the GAGs was evaluated by activated partial thromboplastin time (aPTT ) assay and thrombin time (TT) assay. The GAGs of porcine testis markedly increased the clotting times of both of aPTT and TT. showing that PT-Gag-16% NaCl was more effective than PT-Gag-1.5% NaCl. The immunomodulating activity of the GAGs was examined in relation to regulation of cytokine production of mutine peritoneal macrophages. Treatment with the GAGs promonently enhanced the prodution of cytokines. IFN-${\gamma}$, from macrophages. Taken together. GAGs isolated from porcine testis possess biological functions such as anticoagulant and immunomodulating activity.

  • PDF

P-Selectin-mediated Acute Inflammation Can Be Blocked by Chemically Modified Heparin, RO-Heparin

  • Gao, Yanguang;Li, Na;Fei, Rui;Chen, Zhihong;Zheng, Sheng;Zeng, Xianlu
    • Molecules and Cells
    • /
    • 제19권3호
    • /
    • pp.350-355
    • /
    • 2005
  • Selectins are carbohydrate-binding cell adhesion molecules that play a major role in the initiation of inflammatory responses. Heparin can bind to P-selectin, and its anti-inflammatory property is mainly due to inhibition of P-selectin. However, the strong anticoagulant activity of heparin limits its clinical use. We prepared periodate-oxidized, borohydride-reduced heparin (RO-heparin) by chemical modification and tested its anticoagulant and anti-inflammatory activities. Activated partial thromboplastin time (aPTT) assays showed that, compared with heparin, RO-heparin had greatly reduced anticoagulant activity. Intravenous administration of this compound led to reduction in the peritoneal infiltration of neutrophils in a mouse acute inflammation model. In vitro cell adhesion experiments demonstrated that the effect of RO-heparin on inflammatory responses was mainly due to inhibiting the interaction of P-selectin with its ligands. These results indicate that RO-heparin may be a safer treatment for inflammation than heparin, especially when selectin is targeted.

Prophetic Medicine-Nigella Sativa (Black Cumin Seeds) - Potential Herb for COVID-19?

  • Maideen, Naina Mohamed Pakkir
    • 대한약침학회지
    • /
    • 제23권2호
    • /
    • pp.62-70
    • /
    • 2020
  • Coronavirus disease-19 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (SARS CoV-2). Currently, the management of patients with COVID-19 depends mainly on repurposed drugs which include chloroquine, hydroxychloroquine, lopinavir/ritonavir, ribavirin, remdesivir, favipiravir, umifenovir, interferon-α, interferon-β and others. In this review, the potential of Nigella sativa (black cumin seeds) to treat the patients with COVID-19 analyzed, as it has shown to possess antiviral, antioxidant, anti-inflammatory, anticoagulant, immunomodulatory, bronchodilatory, antihistaminic, antitussive, antipyretic and analgesic activities. Medline/PubMed Central/PubMed, Google Scholar, Science Direct, Directory of open access journals (DOAJ) and reference lists were searched to identify articles associated with antiviral and other properties of N.sativa related to the signs and symptoms of COVID-19. Various randomized controlled trials, pilot studies, case reports and in vitro and in vivo studies confirmed that N.sativa has antiviral, antioxidant, anti-inflammatory, immunomodulatory, bronchodilatory, antihistaminic, antitussive activities related to causative oraganism and signs and symptoms of COVID-19. N. sativa could be used as an adjuvant therapy along with repurposed conventional drugs to manage the patients with COVID-19.

Biological activities of ethanolic extract from Robinia pseudoacacia L. flower

  • Han, Myeong Gyu;Park, Yu Jin;In, Man-Jin;Kim, Dong Chung
    • Journal of Applied Biological Chemistry
    • /
    • 제65권2호
    • /
    • pp.107-111
    • /
    • 2022
  • Biological activities such as antioxidant, anticoagulant, and α-glucosidase inhibitory effects of 40% (v/v) ethanolic extract from black locust (Robinia pseudoacacia L.) flower were investigated. The polyphenol content of the black locust flower extract was 39.8±0.5 mg gallic acid equivalents/g. The flower extract represented antioxidant effects such as free radical, cationic radical, and nitrite scavenging abilities as well as reducing power. Also the flower extract inhibited α-glucosidase activity and common pathway in plasma coagulation system.

의약품으로 개발된 Pyridazine 유도체 (Pyridazine Derivatives Developed as Medicines)

  • 권순경
    • Biomolecules & Therapeutics
    • /
    • 제8권1호
    • /
    • pp.1-12
    • /
    • 2000
  • Although the first pyridazine was obtained in 1886, this heterocycle was not thoroughly investigated such isomers as pyrimidine and pyrazine especially in the field of drug development because pyridazine derivatives do not occur as natural products. Recently medicinal chemists have an growing interest in the pyridazine derivatives, since many Pyridazine derivatives were found to possess various potential therapeutic activities. In this paper sixty-eight pyridazine derivatives, which are already introduced as medicines or are being developed as drugs were classified according to their pharmacological activities, reviewed since 1955 and the relationship of structure-activities was discussed.

  • PDF

국내산 미역포자엽, 다시마, 톳, 모자반 fucoidan의 항혈액응고 특성 (Blood-Anticoagulant Activity of Fucoidans from Sporophylls of Undaria pinnatifida, Laminaria religiosa, Hizikia fusiforme and Sargassum fulvellum in Korea)

  • 구재근;최용석;곽중기
    • 한국수산과학회지
    • /
    • 제34권5호
    • /
    • pp.515-520
    • /
    • 2001
  • 국내 연안에서 생산되고 있는 갈조류인 미역포자엽, 다시마, 톳, 모자반을 묽은 염산 (pH 2.0)으로 $65^{\circ}C$에서 추출한 crude fucoidan을 CPC처리하여 침전시킨 후 $CaCl_2$ 농도 (1.0M, 1.5M, 3.0M)를 증가시키면서 분획하였다. APTT 활성으로 비교한 결과 분획물의 항 혈액응고 활성은 황산기의 함량이 증가할수록 증가하였으며, 분획물 시료중 미역포자엽을 3.0M $CaCl_2$로 분획한 것이 가장 활성이 우수하였다. 이 획분을 다시 pronase와 laminase로 수식한 결과 각각 단백질과 glucose가 감소하였으나 수식 전에 비하여 APTT 활성이 증가하였다. Pronase와 laminase로 수식한 fucoidan의 fucose : galactose : mannose : sulfate : uronic acid의 $mole\%$는 1 : 1.3:0.03:2.7:0.08이였으며, 효소 처리에 따른 미역 포자엽의 주 결합구조는 변화가 없었다.

  • PDF

스피루리나 효소가수분해물의 생리활성 탐색 (Investigation of Biological Activities of Enzymatic Hydrolysate of Spirulina)

  • 손민희;박근형;최아름;유귀재;인만진;김동호;채희정
    • 한국식품영양과학회지
    • /
    • 제38권2호
    • /
    • pp.136-141
    • /
    • 2009
  • 스피루리나를 세포벽 가수분해효소와 단백질 가수분해효소로 처리하여 조제한 스피루리나 가수분해물(enzymatic hydrolysate of spirulina, EHS)의 생리활성을 조사하였다. 효소처리 가수분해물의 유산균 증식효과, 항산화능, 암세포 증식저해 활성, 항혈전 활성을 분석한 결과 EHS는 유산균 증식활성과 항산화능에 큰 영향을 미치지 않았으며, 자궁경부암세포(HeLa)에 대해 1.42 mg/L의 농도에서 15% 미만의 증식저해효과를 나타내었다. 반면 항혈전 활성을 공통 경로(common pathway), 내인성 경로(intrinsic pathway), 외인성 경로(extrinsic pathway)로 구분하여 측정한 결과, 공통경로, 내인성 경로와 유사한 항혈전 활성이 있음을 확인하였다. 공통 경로를 thrombin time assay로 측정한 결과 EHS의 농도가 100 mg/L일 때 155.6초를 나타내었다. 내인성 경로는 activated partial thromboplastin time assay로 측정하였고, EHS의 농도가 1000 mg/L일 때 95.8초를 나타내었다. 외인성 경로를 prothrombin time assay로 측정한 결과 EHS의 농도가 1000 mg/L일 때 10.6초를 나타내었다. 결과적으로 스피루리나 효소가수분해물(EHS)이 항혈전경로 중 공통경로와 내인성 경로에 활성이 있음을 알 수 있었으며, 이를 토대로 신규의 항혈전 기능성 원료로 개발될 수 있을 것으로기대된다.

Evaluation of the in vivo Antithrombotic, Anticoagulant and Fibrinolytic Activities of Lumbricus rubellus Earthworm Powder

  • Hahn, Bum-Soo;Jo, You-Young;Yang, Kyung-Youl;Wu, Song-Ji;Pyo, Mi-Kyung;Yunchoi, Hye-Sook;Kim, Yeong-Shik
    • Archives of Pharmacal Research
    • /
    • 제20권1호
    • /
    • pp.17-23
    • /
    • 1997
  • A saline suspension of Lumbricus rubellus earthworm powder (EWP) was administered to rats (1 g/kg/day) orally for 15 days to evaluate an oral effectiveness for thrombotic disorders. Blood was drawn at 2-day interval after the administration. Several parameters for antithrombotic, anticoagulant and fibrinolytic activities were measured, including platelet aggregation, clotting time, plasmin activity and the levels of FDP (fibrin/fibrinogen degradation products), D-dimer, and t-PA antigen. It did not affect platelet aggregation induced by ADP and collagen but anticoagulant activity (aPTT and TT) was gradually increased to two-folds for the first 5 days of administration and back to normal. Fibrinolytic activity of euglobulin fraction was highest on the 11 th day after the administration. The level of FDP was elevated to be comparable to the positve control$ (5-10 {\mu}g/ml)$ after 9-day treatment. Oral administration of the EWP could also reduce the formation of venous thrombus induced with viper venom. Complete blood count (CBC) profiles were within normal ranges except for a slight increase in white blood cells after the oral administration for 15 days. These results suggested that the EWP may be valuable for the prevention and/or treatment of thrombotic diseases.

  • PDF

Anticoagulant and Antiplatelet Activities of Artemisia princeps Pampanini and Its Bioactive Components

  • Ryu, Ri;Jung, Un Ju;Kim, Hye-Jin;Lee, Wonhwa;Bae, Jong-Sup;Park, Yong Bok;Choi, Myung-Sook
    • Preventive Nutrition and Food Science
    • /
    • 제18권3호
    • /
    • pp.181-187
    • /
    • 2013
  • Artemisia princeps Pampanini (AP) has been used as a traditional medicine in Korea, China and Japan and reported to exhibit various beneficial biological effects including anti-inflammatory, antioxidant, anti-atherogenic and lipid lowering activities; however, its antiplatelet and anticoagulant properties have not been studied. In the present study, we evaluated the effects of an ethanol extract of Artemisia princeps Pampanini (EAP) and its major flavonoids, eupatilin and jaceosidin, on platelet aggregation and coagulation. To determine the antiplatelet activity, arachidonic acid (AA)-, collagen- and ADP (adenosine diphosphate)-induced platelet aggregation were examined along with serotonin and thromboxane A2 ($TXA_2$) generation in vitro. The anticoagulant activity was determined by monitoring the activated partial thromboplastin time (aPTT) and prothrombin time (PT) in vitro. The data showed that EAP and its major flavonoids, eupatilin and jaceosidin, significantly reduced AA-induced platelet aggregation and the generation of serotonin and $TXA_2$, although no significant change in platelet aggregation induced by collagen and ADP was observed. Moreover, EAP significantly prolonged the PT and aPTT. The PT and/or aPTT were significantly increased in the presence of eupatilin and jaceosidin. Thus, these results suggest that EAP may have the potential to prevent or improve thrombosis by inhibiting platelet activation and blood coagulation.