Kini / Clemetson / Markland Toxins and Hemostasis
1. Auflage 2010
ISBN: 978-90-481-9295-3
Verlag: Springer Netherland
Format: PDF
Kopierschutz: 1 - PDF Watermark
From Bench to Bedside
E-Book, Englisch, 797 Seiten
Reihe: Biomedical and Life Sciences
ISBN: 978-90-481-9295-3
Verlag: Springer Netherland
Format: PDF
Kopierschutz: 1 - PDF Watermark
Zielgruppe
Research
Autoren/Hrsg.
Weitere Infos & Material
1;Preface;5
2;Acknowledgments;8
3;Contents;10
4;Contributors;14
5;About the Editors;19
6;Introduction;22
7;From Bench to Bedside;31
7.1;From the Bothrops Jararaca Bradykinin Potentiating Peptides to Angiotensin Converting Enzyme Inhibitors;32
8;The Omics – The Search Is On;37
8.1;Sialomic Perspectives on the Evolution of Blood- Feeding Behavior in Arthropods: Future Therapeutics by Natural Design;38
8.2;Snake Venomics, Antivenomics, and Venom Phenotyping: The Ménage à Trois of Proteomic Tools Aimed at Understanding the Biodiversity of Venoms;62
8.3;Insights in to Venom and Toxin Activities and Pharmacological/ Therapeutic Potential Using Gene Expression Profiling;90
8.4;Bioactive Peptides and Proteins from Wasp Venoms;99
8.5;The Theory of Intraspecies Variation is Not the Exception, But Simply the Rule: The Diverse Hemostatic Activities of Snake Venoms;112
8.6;Tiny Ticks are Vast Sources of Antihaemostatic Factors;128
8.7;Sialogenins and Immunomodulators Derived from Blood Feeding Parasites;146
8.8;Salivary Protease Inhibitors with Non Anti- Hemostatic Functions;168
9;Anticoagulant Proteins;180
9.1;Blood Coagulation Factor IX/Factor X- Binding Protein;181
9.2;Bothrojaracin – A Potent Thrombin Inhibitor;192
9.3;Anticoagulant Phospholipases A2 Which Bind to the Specific Soluble Receptor Coagulation Factor Xa;214
9.4;Hematophagy and Inhibition of the Extrinsic and Intrinsic Tenase Complexes;231
9.5;Thrombin Inhibitors from Haematophagous Animals;250
9.6;Anticoagulants from Scorpion Venoms;266
10;Antiplatelet Proteins;278
10.1;The Discovery of Disintegrins;279
10.2;Brief History and Molecular Determinants of Snake Venom Disintegrin Evolution;295
10.3;Anti-Angiogenesis and Disintegrins;311
10.4;Hematophagy and Inhibition of Platelet Aggregation;340
10.5;Snaclecs (Snake C-Type Lectins) that Inhibit Platelet Receptors;367
11;Fibrinolytic Proteins;377
11.1;Plasminogen Activators from Snake Venoms;378
11.2;Bat Plasminogen Activator: Desmoteplase – From Bat to Bench to Bedside of Stroke Victims;400
11.3;Fibrolase and Its Evolution to Clinical Trials: A Long andWinding Road;415
11.4;Streptokinase;434
12;Procoagulant Proteins;450
12.1;Activation of Factor X by Snake Venom Proteases;451
12.2;Structural Aspects of the Factor X Activator RVV- X from Russell’s Viper Venom;469
12.3;Snake Venom Prothrombin Activators – The History;489
12.4;Origin and Evolution of Snake Venom Prothrombin Activators;504
12.5;Thrombin-Like Enzymes in Snake Venoms;521
12.6;Procoagulant Factors from Lonomia Caterpillars;560
12.7;Staphylocoagulase;576
12.8;Procoagulant Properties of Plant Latex Proteases;592
13;Platelet Aggregation Inducers;605
13.1;The Biologic Activity of Aggretin/Rhodocytin, a Snake Venom C- Type Lectin Protein ( Snaclec);606
13.2;Snaclecs (Snake C-Type Lectins) that Activate Platelets;620
13.3;The Effect of Bacterial Toxins on Platelet Function;636
14;Hypotensive Factors;651
14.1;Hypertensive and Hypotensive Snake Venom Components;652
14.2;Hypotensive Proteins from Hematophagous Animals;670
15;Hemorrhage and Coagulopathies;694
15.1;Snakebite-Induced Coagulopathy and Bleeding Disorders;695
15.2;Antivenoms and Coagulation;707
15.3;Biological Activities of Snake Venom Metalloproteinases on Platelets, Neutrophils, Endothelial Cells, and Extracellular Matrices;718
16;Applications;728
16.1;Leeches in Microsurgery – An Evidence-Based Approach;729
16.2;Diagnostic Use of Snake Venom Components in the Coagulation Laboratory;740
17;Index;760