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Blood clotting inhibition

Physiological responses to prostaglandins encompass a variety of effects Some prostaglandins relax bronchial muscle others contract it Some stimulate uterine con tractions and have been used to induce therapeutic abortions PGEj dilates blood vessels and lowers blood pressure it inhibits the aggregation of platelets and offers promise as a drug to reduce the formation of blood clots... [Pg.1080]

Calcium is essential to several steps in the enzyme cascade of the blood clotting process, such as the conversion of prothrombin to thrombin (23). Clotting can be inhibited in stored blood suppHes by addition of complexing agents such as EDTA or citrate which reduce the levels of the free ion, Ca(Il). [Pg.409]

Because these compounds are acidic, they can cause stomach irritation unless taken with food or water. Beyond that, aspirin inhibits blood clotting, which explains why it is often prescribed to reduce the likelihood of a stroke or heart attack. Indeed, it is now recommended for a person in the throes of a heart attack. [Pg.374]

Heparin inhibits the formation of fibrin clots, inhibits the conversion of fibrinogen to fibrin, and inactivates several of the factors necessary for the clotting of blood. Heparin cannot be taken orally because it is inactivated by gastric acid in the stomach therefore, it must be given by injection. Heparin has no effect on clots that have already formed and aids only in preventing the formation of new blood clots (thrombi). The LMWHs act to inhibit clotting reactions by binding to antithrombin HI, which inhibits the synthesis of factor Xa and the formation of thrombin. [Pg.424]

Aspirin is known to inhibit blood clotting. Explain why surgeons recommend that no aspirin be taken immediately before or after surgery. [Pg.68]

Anticoagulant Any substance that inhibits, suppresses, or delays the formation of blood clots. These substances occur naturally and regulate the clotting cascade. Several anticoagulants have been identified in a variety of animal tissues and have been commercially developed for therapeutic use. [Pg.1560]

UK is a serine protease that activates plasminogen to plasmin. Plasmin dissolves the fibrin in blood clots. The attachment of UK to the islet surface was expected to dissolve blood clots that surrounded the islets in the liver thus, IBMIR could be inhibited in the initial stages. A fibrin plate-based assay was performed to assess the... [Pg.190]

In apoptosis a series of events takes place in an orderly sequence involving the activation of various proteases which are called caspases, for cysteine and aspartate proteases. Several distinct caspases act in a cascade vaguely reminiscent of the blood-clotting cascade of complement proteins. If one wishes to interfere with the apoptotic process, then one strategy would be to develop drugs that inhibit various caspases, a current effort underway in the pharmaceutical industry. [Pg.71]

Since predators of snakes (and humans) have to deal with snake venoms as defenses, they are included here, even though they serve in predation. Snake venoms are primarily enzymes (proteins), especially of the phospholipase A2 type, which breaks down cell membrane phospholipids hydrolytically. Other snake venoms such as cobrotoxin contain peptides with 60-70 amino acid residues. Pharmacologically, they have neurotoxic, cytotoxic, anticoagulant, and other effects. The neurotoxins, in turn, can have pre- or postsynaptic effects. Snake venoms with both neurotoxic and hemolytic effects on the heart are known as cardiotoxins. Cytotoxins attach to the cells of blood vessels and cause hemorrhage. Snake venom factors may stimulate or inhibit blood clotting. Finally, platelet-active factors can contribute to hemorrhage. [Pg.257]

The fibrin thrombus resulting from blood clotting (see p. 290) is dissolved again by plasmin, a serine proteinase found in the blood plasma. For this purpose, the precursor plasminogen first has to be proteolyti-cally activated by enzymes from various tissues. This group includes the plasminogen activator from the kidney (urokinase) and tissue plasminogen activator (t-PA) from vascular endothelia. By contrast, the plasma protein a2-antiplasmin, which binds to active plasmin and thereby inactivates it, inhibits fibrinolysis. [Pg.292]

Rodenticides are a broad class of chemicals designed to kill mammals, particularly rats and mice. Compounds that inhibit blood clotting, anticoagulants, are commonly used to control rat populations. One of the first was warfarin, which is related to the plant-derived coumadin (from spoiled sweet clover). In the 1950s rats developed resistance to warfarin, which prompted the development of more potent anticoagulants. Other rodenticides include fluoroacetic acid and zinc phosphide (very toxic) and thiourea-based compounds. The primary alternative to using rodenticides is trapping. [Pg.79]

Therapy with heparin occurs in an inpatient setting. Heparin inhibits both in vitro and in vivo clotting of blood. Whole blood clotting time and activated partial thromboplastin time (aPTT) are prolonged in proportion to blood heparin concentrations. [Pg.259]

The salicylates are also potent antipyretic agents, with the exception of diflunisal, which is only weakly active. Aspirin acts at two distinct but related sites. It decreases prostaglandin-induced fever in response to pyrogens and induces a decrease in interleukin-1 modulation of the hypothalamic control of body temperature. Thus, the hypothalamic control of body temperature returns, vasodilation occurs, heat dissipates, and fever decreases. Other uses of aspirin include inhibition of platelet aggregation via inhibition of thromboxanes, which has been shown to decrease the incidence of blood clots, myocardial infarction, and transient ischemic attacks. [Pg.313]


See other pages where Blood clotting inhibition is mentioned: [Pg.434]    [Pg.434]    [Pg.242]    [Pg.259]    [Pg.235]    [Pg.606]    [Pg.91]    [Pg.616]    [Pg.86]    [Pg.225]    [Pg.177]    [Pg.685]    [Pg.25]    [Pg.98]    [Pg.248]    [Pg.46]    [Pg.376]    [Pg.168]    [Pg.55]    [Pg.620]    [Pg.277]    [Pg.60]    [Pg.1439]    [Pg.51]    [Pg.323]    [Pg.323]    [Pg.131]    [Pg.142]    [Pg.427]    [Pg.542]    [Pg.29]    [Pg.31]    [Pg.523]    [Pg.52]    [Pg.9]    [Pg.429]    [Pg.1]    [Pg.126]   
See also in sourсe #XX -- [ Pg.622 ]

See also in sourсe #XX -- [ Pg.622 ]

See also in sourсe #XX -- [ Pg.622 ]

See also in sourсe #XX -- [ Pg.141 ]

See also in sourсe #XX -- [ Pg.622 ]




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