In
1940s a specific antagonist for folic acid is developed for first time known as
Methotrexate which inhibits the proliferation of malignant cells basically byinhibiting the de novo synthesis of purines and pyrimidines. The presented
study concludes that the acute exposure to Methotrexate produced no appreciable
changes but in routine consultation of oxidative stress parameters including
the glutathione metabolizing system in patients using long term MTX cure can be
considered.
Methotrexate is a folic acid
antagonist, widely used as a chemotherapeutic agent in the treatment of various
cancerous stages (leukaemia, lymphoma, osteosarcoma, head and neck tumours,
lung cancer, breast cancer, etc.) and in the treatment of various inflammatory
diseases. It is also used for the treatment of multiple sclerosis,dermatomyositis, sarcoidosis, psoriasis, and rheumatoid arthritis, disorders
causing inflammation. Its side effects include hypersensitivity pneumonia,
central and peripheral nervous system toxicity, liver and gastrointestinal
system dysfunctions and hematologic failure.
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