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Metabolism of rabbit angiostatin glycoforms I and II in rabbits: angiostatin-I leaves the intravascular space faster and appears to have greater anti-angiogenic activity than angiostatin-II.
- Source :
-
The Journal of laboratory and clinical medicine [J Lab Clin Med] 2001 Aug; Vol. 138 (2), pp. 83-93. - Publication Year :
- 2001
-
Abstract
- Plasminogen (PLG) exists in the circulation as two glycoforms, I and II. Angiostatin (AST) is a polypeptide that has been cleaved from the kringle region of PLG and has strong anti-angiogenic properties. AST-I and AST-II, which consisted only of kringles 1 through 3, were prepared by the action of urokinase on purified rabbit PLG-I and PLG-II, respectively, in the presence of N-acetyl cysteine, followed by affinity chromatography on lysine-Sepharose. Purified AST-I and AST-II were tested for functional activity with a chick chorioallantoic membrane (CAM) model; when similar amounts were applied to a 6-day CAM, AST-I was substantially more effective than AST-II in decreasing vascular supply to the CAM over a 72-hour period; this activity correlated with a loss of capillaries, probably through apoptosis of endothelial cells. Radiolabeled AST-I and AST-II (iodine 125 and iodine 131) were co-injected intravenously into healthy rabbits to determine their clearances from plasma measured over 3 days. Over a dose range of 0.08 to 2.7 microg/kg, the fractional catabolic rate within the intravascular space (j(3)) indicated that AST-I was cleared 3-fold to 4-fold more rapidly than AST-II (P < .001). The catabolic half-life of AST-I (2.01 +/- 0.19 days) was significantly less than that of AST-II (2.62 +/- 0.20 days). The faster clearance of AST-I from the intravascular space was matched by its more rapid passage than AST-II to the extravascular space of various organs over 60 minutes in vivo. This property of AST-I as compared with AST-II may partially explain its greater anti-angiogenic potential. From the plasma concentrations of PLG-I and PLG-II and their relative behaviors toward rabbit VX-2 lung tumors in vivo, we predict that substantially greater quantities of AST-II than AST-I may be released into the extravascular space of tumors.
- Subjects :
- Angiostatins
Animals
Capillaries metabolism
Chick Embryo
Endothelium, Vascular metabolism
Iodine Radioisotopes
Isomerism
Peptide Fragments chemistry
Peptide Fragments isolation & purification
Plasminogen chemistry
Plasminogen isolation & purification
Rabbits
Species Specificity
Tarsal Joints metabolism
Neovascularization, Physiologic drug effects
Peptide Fragments pharmacokinetics
Plasminogen pharmacokinetics
Subjects
Details
- Language :
- English
- ISSN :
- 0022-2143
- Volume :
- 138
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- The Journal of laboratory and clinical medicine
- Publication Type :
- Academic Journal
- Accession number :
- 11477374
- Full Text :
- https://doi.org/10.1067/mlc.2001.116679