The protective properties of synthetic porphyrin tin complexes in toxic hyperbilirubinemia
β Scribed by T. O. Philippova; B. N. Galkin; N. Ya. Golovenko; Z. I. Zhilina; S. V. Vodzinskii
- Book ID
- 101290502
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 112 KB
- Volume
- 04
- Category
- Article
- ISSN
- 1088-4246
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β¦ Synopsis
Tin complexes of meso-substituted synthetic porphyrins, namely Sn^4+^-meso-tetraphenyl- porphyrin ( Sn - TPP ) and Sn^4+^-meso-tetrakis(N-methyl-3-pyridyl)porphyrin tetratosylate ( Sn - TMe -3- PyP ), efficiently decrease the serum bilirubin level when injected subcutaneously at a dose of 100 ΞΌM kg^β1^body weight into mice. These compounds are active during hyperbilirubinemia, induced by phenylhydrazine, hemin and tetrachloromethane, and also during autoimmune hemolytic anemia. In the latter case a decrease in serum bilirubin content was observed, as well as a decrease in the amount of blood reticulocytes which reflects a milder course of the disease. The Sn complexes under study induce, in vivo, cytochrome P-450, inhibit microsomal heme oxygenase and decrease the intensity of lipid peroxidation. At the same time, in vitro the hepatic and splenic heme oxygenase activity is blocked only when a 0.1 ΞΌM concentration of Sn - TMe -3- PyP or Sn -protoporphyrin IX is added to the incubation mixture. Sn - TPP does not affect the activity of this enzyme in vitro.
π SIMILAR VOLUMES
The mono-and bidentate chelation of the main-group related bis(diamino)-and the higher element homologue bis(diarsanyl)methanide ligand systems have been studied. elements silicon, germanium, tin, and lead through the phosphorus atoms of the diphosphanylmethanide ligand has The bonding situation in