PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2004 | 51 | 1 |

Tytuł artykułu

Glutathione S-transferase pi as a target for tricyclic antidepressants in human brain

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
GST pi, the main glutathione S-transferase isoform present in the human brain, was isolated from various regions of the brain and the in vitro effect of tricyclic anti­depressants on its activity was studied. The results indicated that amitripyline and doxepin — derivatives of dibenzcycloheptadiene, as well as imipramine and clomipramine — derivatives of dibenzazepine, inhibit the activity of GST pi from frontal and parietal cortex, hippocampus and brain stem. All these tricyclics are non- competitive inhibitors of the enzyme with respect to reduced glutathione and non- competitive (amitripyline, doxepin) or uncompetitive (imipramine, clomipramine) with respect to the electrophilic substrate. Their inhibitory effect is reversible and it depends on the chemical structure of the tricyclic antidepressants rather than on the brain localization of the enzyme. We conclude that the interaction between GST pi and the drugs may reduce their availability in the brain and thus affect their therapeutic activity. On the other hand, tricyclic antidepressants may decrease the efficiency of the enzymatic barrier formed by GST and increase the exposure of brain to toxic electrophiles. Reactive electrophiles not inactivated by GST may contribute in adverse effects caused by these drugs.

Wydawca

-

Rocznik

Tom

51

Numer

1

Opis fizyczny

p.207-212,fig.,ref.

Twórcy

  • Medical University of Warsaw, S.Banacha 1, 02-097 Warsaw, Poland
autor
autor
autor

Bibliografia

  • Ali-Osman F, Brunner JM, Kutluk TM, Hess K. (1997) Prognostic significance of glutathione 5-transferase pi expression and subcellular localization in human gliomas. Clin Cancer Res.; 3: 2253-61.
  • Baranczyk-Kuzma A, Barszczewska I, Audus KL. (1992) The effect of endo- and exogenous compounds on the activity of glutathione 5-transferase from monkey brain. Acta Biochim Polon.; 39: 133-8.
  • Baranczyk-Kuzma A, Drobisz D. (1993) Heterogeneity of bovine brain glutathione 5-transferase. Acta Biochim Polon.; 40: 100-2.
  • Board P, Coggan M, Johnston P, Ross V, Suzuki T, Webb G. (1990) Genetic heterogeneity of the human glutathione 5- transferases: a complex of gene families. Pharmacol Ther.; 48: 357-69.
  • Bradford MM. (1976) A rapid and sensitive method for the quantitation of microgram quantities of proteins utilizing the principle of protein-dye binding. Anal Biochem.; 72: 248-54.
  • Habig WB, Pabst MJ, Jakoby WB. (1974) Glutathione 5-transferases. The first step in mercapturic acid formation. J Biol Chem.; 249: 7130-9.
  • Jakoby WB. (1987) The glutathione 5-transferases: a group of multifunctional detoxication proteins. AdvEnzymol.; 46: 383-414.
  • Kamisaka K, Listowsky I, Gaitmaita Z, Arias IM. (1975) Interactions of bilirubin and other ligands with ligandin. Biochemistry.; 14: 2175-80.
  • Kostowski W. (1998) Antidepressant drugs. In Pharmacology, Kostowski W, ed, pp 845-76, PZWL, Warsaw, Poland.
  • Listowsky I, Abramowitz M, Homma H, Niitsu Y. (1988) Intracellular binding of hormones and xenobiotics by glutathione 5-transferases. DrugMetab Rev.; 19: 305-18.
  • Oakley AJ, Lo Bello M, Nuccetelli M, Mazzetti AP, Parker MW. (1999) The ligandin (non-substrate) binding site of human pi class glutathione transferase is located in the electrophile binding site (H-site). JMol Biol.; 291: 913-26.
  • Sawicki J, Kuzma M, Maslinski S, Baranczyk-Kuzma A. (1997) Effect of biogenic amines and their derivatives on glutathione conjugation in brain. J Physiol Pharmacol.; 48 Suppl 2: 100-9.
  • Sawicki J, Kuzma M, Baranczyk-Kuzma A. (2001) The effect of serotonin, its precursors and metabolites on brain glutathione 5-transferase. Neurochem Res.; 26: 469-72.
  • Theodore C, Singh SV, Hong TD, Awasthi YC. (1985) Glutathione 5-transferases of human brain. Evidence for two immunologically distinct types of 26500-Mr subunits. Biochem J. ; 225: 375-82.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-6f317344-92da-4d50-8d37-c1ac3476f41b
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.