Biochemical and Biophysical Research Communications, Vol.318, No.1, 53-59, 2004
High molecular mass kininogen inhibits metalloproteinases of Bothrops jararaca snake venom
High molecular mass kininogen (HK) purified from Bothrops jararaca (Bj) plasma was tested on activities of the Bj venom in vivo and in vitro. Results showed that, when incubated with BjHK, the Bj venom presented inhibition on hemorrhagic, edema forming, myotoxic, and coagulant activities. It is well known that metalloproteinases are directly or indirectly involved in these activities. Similarly, human HK inhibits the hemorrhagic effect of the Bj venom as well as hemorrhagic and enzymatic effects of jararhagin, a hemorrhagic metalloproteinase isolated from Bj venom. Complex between HK and jararhagin was not detected by gel filtration. Nevertheless, the inhibitory effect of the hemorrhagic activity of the venom was only partial when HK was pre-incubated with 0.4 mM ZnCl2 or with 0.45 mM CaCl2. These data suggest that the inhibitory effect depends, at least partially, on the competition for ions between kininogen and metalloprotemases of the venom. (C) 2004 Elsevier Inc. All rights reserved.
Keywords:Bothrops jararaca;snake venom;metalloproteinase;proteinase inhibitors;high molecular mass kininogen