Abstract
5-Methyltetrahydrofolate homocysteine methyltransferase activity in human bone marrow cells obtained from patients undergoing surgical operation became low after about 4 hr of nitrous oxide (N2O) anesthesia. The deoxyuridine suppression test performed on these bone marrow cells also became abnormal after about 6 hr of N2O anesthesia. The incorporation of [3H]thymidine into DNA in the bone marrow cells preincubated with methionine or methotrexate was much higher after N2O anesthesia than before anesthesia. Since N2O and methionine or methotrexate have a synergistic effect on depletion of functional folate, N2O alone or in combination with methionine or methotrexate might be of value for cancer treatment and deserve clinical trials.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase / antagonists & inhibitors
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5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase / metabolism*
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Bone Marrow / drug effects*
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Bone Marrow / enzymology
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Bone Marrow / pathology
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DNA / biosynthesis
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Deoxyuridine / metabolism
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Drug Synergism
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Folic Acid Antagonists*
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Humans
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Methionine / pharmacology*
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Methotrexate / pharmacology*
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Methyltransferases / metabolism*
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Neoplasms / drug therapy
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Nitrous Oxide / pharmacology*
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Pteroylpolyglutamic Acids / metabolism
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Time Factors
Substances
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Folic Acid Antagonists
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Pteroylpolyglutamic Acids
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DNA
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Methionine
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Methyltransferases
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5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase
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Nitrous Oxide
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Deoxyuridine
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Methotrexate