Effect of supplemental folic acid on valproic acid-induced embryotoxicity and tissue zinc levels in vivo

Valproic acid (VPA) is an anticonvulsant drug known to cause spina bifida in humans. Administration of the vitamin, folic acid has been reported to decrease the frequency of VPA‐induced exencephaly in mice treated with the drug in vivo. A protective effect by folinic acid has not been observed in vi...

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Veröffentlicht in:Teratology (Philadelphia) 1995-11, Vol.52 (5), p.277-285
Hauptverfasser: Hansen, Deborah K., Grafton, Thomas F., Dial, Stacey L., Gehring, Theresa A., Siitonen, Paul H.
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container_end_page 285
container_issue 5
container_start_page 277
container_title Teratology (Philadelphia)
container_volume 52
creator Hansen, Deborah K.
Grafton, Thomas F.
Dial, Stacey L.
Gehring, Theresa A.
Siitonen, Paul H.
description Valproic acid (VPA) is an anticonvulsant drug known to cause spina bifida in humans. Administration of the vitamin, folic acid has been reported to decrease the frequency of VPA‐induced exencephaly in mice treated with the drug in vivo. A protective effect by folinic acid has not been observed in vitro. The purpose of this investigation was to reexamine the ability of folinic acid to decrease the incidence of VPA‐induced neural tube defects in vivo. We also examined the effect of increased intake of folic acid on zinc levels in various maternal and embryonic tissues. Folinic acid, whether administered by intraperitoneal injection or in osmotic mini‐pumps, did not decrease the number of mouse fetuses with VPA‐induced exencephaly. Dietary supplementation with 10–20 times the daily required intake of folic acid in rodents also failed to decrease the embryotoxicity of VPA. Such dietary supplementation had no effect on zinc levels in maternal liver, brain, or kidney, nor in embryonic tissues. These results indicate that folic acid is not able to reverse the embryotoxicity induced by the anticonvulsant, that there is no apparent effect of high dietary folate intake on maternal or embryonic zinc levels and suggest that folate is probably not involved in the mechanism of VPA‐induced embryotoxicity. © 1995 Wiley‐Liss, Inc.
doi_str_mv 10.1002/tera.1420520506
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Administration of the vitamin, folic acid has been reported to decrease the frequency of VPA‐induced exencephaly in mice treated with the drug in vivo. A protective effect by folinic acid has not been observed in vitro. The purpose of this investigation was to reexamine the ability of folinic acid to decrease the incidence of VPA‐induced neural tube defects in vivo. We also examined the effect of increased intake of folic acid on zinc levels in various maternal and embryonic tissues. Folinic acid, whether administered by intraperitoneal injection or in osmotic mini‐pumps, did not decrease the number of mouse fetuses with VPA‐induced exencephaly. Dietary supplementation with 10–20 times the daily required intake of folic acid in rodents also failed to decrease the embryotoxicity of VPA. Such dietary supplementation had no effect on zinc levels in maternal liver, brain, or kidney, nor in embryonic tissues. These results indicate that folic acid is not able to reverse the embryotoxicity induced by the anticonvulsant, that there is no apparent effect of high dietary folate intake on maternal or embryonic zinc levels and suggest that folate is probably not involved in the mechanism of VPA‐induced embryotoxicity. © 1995 Wiley‐Liss, Inc.</description><identifier>ISSN: 0040-3709</identifier><identifier>EISSN: 1096-9926</identifier><identifier>DOI: 10.1002/tera.1420520506</identifier><identifier>PMID: 8838251</identifier><identifier>CODEN: TJADAB</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Anticonvulsants - toxicity ; Biological and medical sciences ; Circadian Rhythm ; Drug Interactions ; Drug toxicity and drugs side effects treatment ; Embryo, Mammalian - chemistry ; Embryonic and Fetal Development - drug effects ; Female ; Folic Acid - administration &amp; dosage ; Folic Acid - blood ; Folic Acid - pharmacology ; Injections, Intraperitoneal ; Injections, Subcutaneous ; Male ; Medical sciences ; Mice ; Miscellaneous (drug allergy, mutagens, teratogens...) ; Pharmacology. 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These results indicate that folic acid is not able to reverse the embryotoxicity induced by the anticonvulsant, that there is no apparent effect of high dietary folate intake on maternal or embryonic zinc levels and suggest that folate is probably not involved in the mechanism of VPA‐induced embryotoxicity. © 1995 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>8838251</pmid><doi>10.1002/tera.1420520506</doi><tpages>9</tpages></addata></record>
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ispartof Teratology (Philadelphia), 1995-11, Vol.52 (5), p.277-285
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subjects Animals
Anticonvulsants - toxicity
Biological and medical sciences
Circadian Rhythm
Drug Interactions
Drug toxicity and drugs side effects treatment
Embryo, Mammalian - chemistry
Embryonic and Fetal Development - drug effects
Female
Folic Acid - administration & dosage
Folic Acid - blood
Folic Acid - pharmacology
Injections, Intraperitoneal
Injections, Subcutaneous
Male
Medical sciences
Mice
Miscellaneous (drug allergy, mutagens, teratogens...)
Pharmacology. Drug treatments
Pregnancy
Rats
Tissue Distribution
Valproic Acid - administration & dosage
Valproic Acid - toxicity
Zinc - chemistry
title Effect of supplemental folic acid on valproic acid-induced embryotoxicity and tissue zinc levels in vivo
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