An-Najah University Journal for Research - A (Natural Sciences)

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An-Najah University Journal for Research - A (Natural Sciences) Indexed in Scopus since 2019
CiteScore 0.8
Indexed since 2019
First decision 5 Days
Submission to acceptance 160 Days
Acceptance to publication 20 Days
Acceptance rate 14%

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original_full_paper

Brugia Malayi: Depletion of Glutathione by Buthionine Sulfoximine

Published
2005-08-28
Pages
83 - 90
Full text

Abstract

Glutathione is an intracellular reducing agent. It is synthesized by a two-step reaction catalyzed by ?-glutamylcysteine synthetase (?GCS) and glutathione synthetase. ?GCS, which is the rate limiting enzyme in the synthesis of glutathione, is inhibited specifically by buthionine sulfoximine (BSO). The enzyme was partially purified from the parasitic nematode Brugia malayi, the causative agents of lymphatic filaraiasis. BSO inhibits the enzyme activity in an irreversible manner. The Brugia enzyme was found to be 24-fold more sensitive to BSO than its mammalian counterparts. The inhibitor was also found effective in depleting the glutathione contents of the parasites with low concentration. The results may conclude that ?GCS is a potential target for the development of drugs against filariasis.

Article history

Received
2004-08-31
Accepted
2005-08-28
Available online
2005-08-28
original_full_paper

Brugia Malayi: Depletion of Glutathione by Buthionine Sulfoximine

Published
2005-08-28
الصفحات
83 - 90
البحث كاملا

الملخص

Glutathione is an intracellular reducing agent. It is synthesized by a two-step reaction catalyzed by ?-glutamylcysteine synthetase (?GCS) and glutathione synthetase. ?GCS, which is the rate limiting enzyme in the synthesis of glutathione, is inhibited specifically by buthionine sulfoximine (BSO). The enzyme was partially purified from the parasitic nematode Brugia malayi, the causative agents of lymphatic filaraiasis. BSO inhibits the enzyme activity in an irreversible manner. The Brugia enzyme was found to be 24-fold more sensitive to BSO than its mammalian counterparts. The inhibitor was also found effective in depleting the glutathione contents of the parasites with low concentration. The results may conclude that ?GCS is a potential target for the development of drugs against filariasis.

Article history

تاريخ التسليم
2004-08-31
تاريخ القبول
2005-08-28
Available online
2005-08-28