The importance of endoparasite counts at necropsy

In a 2-year study of 49 Oklahoma cattle with a typical history of clinical endoparasitism, 12 animals had Ostertagia only, and Ostertagia was the predominant endoparasite in 21. Only 1 animal had a pure Haemonchus population. Though primary endoparasitism was diagnosed antemortem in 32 animals, postmortem worm counts confirmed the diagnosis in only 19. Worm counts documented inapparent disease in 8 animals. In 21 cases of suspected of toxicosis, 12 animals had endoparasitism none was poisoned.     

Heterogeneous reaction probabilities, solubilities, and the physical state of cold volcanic aerosols

On 19 January 1992, heterogeneous loss of HNO(3), ClNO(3), and HCl was observed in part of the Mount Pinatubo volcanic cloud that had cooled as a result of forced ascent. Portions of the volcanic cloud froze near 191 kelvin. The reaction probability of ClNO(3) and the solubility of HNO(3) were close to laboratory measurements on liquid sulfuric acid. The magnitude of the observed loss of HCl suggests that it underwent a heterogeneous reaction. Such reactions could lead to substantial loss of HCl on background sulfuric acid particles and so be important for polar ozone loss.     

Heparin promotes the inactivation of antithrombin by neutrophil elastase

Heparin is an acceleratory cofactor for antithrombin, a circulating inhibitor of blood coagulation enzymes. The presence of heparin on blood vessel walls is believed to contribute to the nonthrombogenic properties of those surfaces. In apparent opposition to this function, heparin was found to greatly accelerate the in vitro inactivation of antithrombin by neutrophil elastase. Inactivation rates in solution were potentiated several hundredfold by specific heparin fractions with anticoagulant activity. Although the data suggest that a heparin-antithrombin complex is essential for the inactivation by elastase to occur, the enzyme itself interacts tightly with heparin. These results suggest a mechanism which, if operating in vivo, could lead to a localized neutralization of the anticoagulant function of heparin at the endothelial surface.