FURTHER EVIDENCE OF BRADYKININ INVOLVEMENT IN SEPTIC SHOCK - REDUCTION OF KININ PRODUCTION IN-VIVO AND IMPROVED SURVIVAL IN RATS BY USE OF POLYMER TAILORED SBTI WITH LONGER T(1 2)/
Yh. Shin et al., FURTHER EVIDENCE OF BRADYKININ INVOLVEMENT IN SEPTIC SHOCK - REDUCTION OF KININ PRODUCTION IN-VIVO AND IMPROVED SURVIVAL IN RATS BY USE OF POLYMER TAILORED SBTI WITH LONGER T(1 2)/, Immunopharmacology, 33(1-3), 1996, pp. 369-373
Involvement of bradykinin in septic shock and its therapeutic endeavor
using soybean trypsin inhibitor (SBTI, Kunitz type) were investigated
in an in vivo model of septic shock induced by pseudomonal elastase.
Pseudomonal elastase injection at 0.5 mg/kg i.v. to guinea pigs result
ed in elevation level of bradykinin in the blood from < 1 ng/ml to 25
ng/ml which was accompanied by a drop of mean arterial blood pressure
(MABP) (about 45 mmHg). When native soybean trypsin inhibitor (SBTI, K
unitz type, 20 kDa) was injected into this model, induction of bradyki
nin generation and hypotension by the bacterial protease treatment was
completely obliterated as judged by the both levels of bradykinin and
MABP. Specifically, by the treatment with SBTI, bradykinin levels did
not increase and the drop of the blood pressure was minimal (< 10 mmH
g) in this time frame (< 30 min). We designed and prepared succinylate
d gelatin-conjugated SBTI (sue-gel SBTI) with enlarged molecular mass
(M(r) similar to 110,000) and higher area under the curve of the plasm
a concentration, which exhibits about 6 times longer plasma half-life
(t(1/2)) and about 4 times larger area under the curve of plasma conce
ntration. Suc-gel-SBTI suppressed the pseudomonal protease-induced sho
ck much more effectively than native SBTI, the conjugate exhibited its
effect for more than 3 h, while the native SBTI showed the effect onl
y within 2 h after i.v. injection.