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Gestational age dependency in the prenatal toxicity and in the disposition kinetics of the novel anticonvulsant HEPP (D,L-3-hydroxy-3-ethyl-3-phenylpropionamide) after subcutaneous administration in pregnant rats.
Int J Toxicol. 2007 May-Jun; 26(3):237-46.IJ

Abstract

HEPP (D,L-3-hydroxy-3-ethyl-3-phenylpropionamide) is a novel anticonvulsant with promising anticonvulsant profile, which is being actively researched. The potential maternal and embryo/fetal toxicities of HEPP were evaluated in pregnant rats following subcutaneous (s.c.) administration during organogenesis (gestation days 6 through 14, GDs 6-14) and the fetal period (GDs 14-21). Single- and multiple-dose pharmacokinetics were also evaluated at the same periods in order to establish possible correlations with some maternal or embryo/fetal toxicity end points. Embryotoxicity was mainly indicated by a significant dose-concentration dependency in the increase in resorptions, high percentage of fully resorbed litters, and decrease in embryo body weights during the GD6-14 dosing period. No gross external alterations were observed in live fetuses. There was no indication of maternal toxicity; but a marked increase in maternal body weight was evident following dosing from GD14 to GD21. The maternal plasma profile following single subcutaneous dose of 50 mg/kg on both GD14 and GD21 showed a monoexponential elimination pattern. Statistically significant differences between treatments (GD14 versus GD21) were observed in elimination (k(el) = 0.12 versus 0.15 h(-1)), absorption (k(a) = 2.01 versus 3.14 h(-1)), maximum plasma concentration time points (T(max) = 1.49 versus 1.01 h); maximum plasma concentration (C(max) = 40.23 versus 36.31 microg/ml) and areas under the concentration-time curve (AUCs(0-infinity) = 421.88 versus 274 microg h/ml. Based on comparisons of C(max), T(max), and AUCs(0-infinity) between the actual data and single intraperitoneal (i.p.) data previously published, the s.c. administration exhibited slower disposition and higher absorbed amount. After multiple-dose administrations of 50 and 100 mg/kg every 12 h (07:00 and 19:00 h), steady-state plasma levels were lower than the computer prediction, and only slight accumulation was observed. In both dosing periods HEPP levels were similar in mothers and offspring at steady-state conditions. The high incidence of embryo death and reduced embryo weight at GD6-14 dosing compared to GD14-21 dosing suggest that embryos are more sensitive to the deleterious effects of HEPP than fetuses; however, the faster elimination observed at late gestation could also contribute to the lower toxicity observed during the fetal period. Because the maternal HEPP plasma levels and the AUC values were positively correlated with embryo/fetal toxicity end points, both pharmacokinetic parameters could be reliable indicators of offspring exposure and consequently of potential toxicity. These data suggest that the length of time that HEPP is present in the maternal plasma at a sufficiently high concentration could be determinant of adverse effects in the offspring.

Authors+Show Affiliations

Departamento de Recursos del Mar, Unidad Mérida, Centro de Investigación y Estudios Avanzados-CINVESTAV, Instituto Politécnico Nacional, Mérida, Yucatán, México. legmartinez@prodigy.net.mx

Pub Type(s)

Journal Article

Language

eng

PubMed ID

17564905

Citation

Gómez-Martínez, Lisbeth E.. "Gestational Age Dependency in the Prenatal Toxicity and in the Disposition Kinetics of the Novel Anticonvulsant HEPP (D,L-3-hydroxy-3-ethyl-3-phenylpropionamide) After Subcutaneous Administration in Pregnant Rats." International Journal of Toxicology, vol. 26, no. 3, 2007, pp. 237-46.
Gómez-Martínez LE. Gestational age dependency in the prenatal toxicity and in the disposition kinetics of the novel anticonvulsant HEPP (D,L-3-hydroxy-3-ethyl-3-phenylpropionamide) after subcutaneous administration in pregnant rats. Int J Toxicol. 2007;26(3):237-46.
Gómez-Martínez, L. E. (2007). Gestational age dependency in the prenatal toxicity and in the disposition kinetics of the novel anticonvulsant HEPP (D,L-3-hydroxy-3-ethyl-3-phenylpropionamide) after subcutaneous administration in pregnant rats. International Journal of Toxicology, 26(3), 237-46.
Gómez-Martínez LE. Gestational Age Dependency in the Prenatal Toxicity and in the Disposition Kinetics of the Novel Anticonvulsant HEPP (D,L-3-hydroxy-3-ethyl-3-phenylpropionamide) After Subcutaneous Administration in Pregnant Rats. Int J Toxicol. 2007 May-Jun;26(3):237-46. PubMed PMID: 17564905.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Gestational age dependency in the prenatal toxicity and in the disposition kinetics of the novel anticonvulsant HEPP (D,L-3-hydroxy-3-ethyl-3-phenylpropionamide) after subcutaneous administration in pregnant rats. A1 - Gómez-Martínez,Lisbeth E, PY - 2007/6/15/pubmed PY - 2007/12/27/medline PY - 2007/6/15/entrez SP - 237 EP - 46 JF - International journal of toxicology JO - Int. J. Toxicol. VL - 26 IS - 3 N2 - HEPP (D,L-3-hydroxy-3-ethyl-3-phenylpropionamide) is a novel anticonvulsant with promising anticonvulsant profile, which is being actively researched. The potential maternal and embryo/fetal toxicities of HEPP were evaluated in pregnant rats following subcutaneous (s.c.) administration during organogenesis (gestation days 6 through 14, GDs 6-14) and the fetal period (GDs 14-21). Single- and multiple-dose pharmacokinetics were also evaluated at the same periods in order to establish possible correlations with some maternal or embryo/fetal toxicity end points. Embryotoxicity was mainly indicated by a significant dose-concentration dependency in the increase in resorptions, high percentage of fully resorbed litters, and decrease in embryo body weights during the GD6-14 dosing period. No gross external alterations were observed in live fetuses. There was no indication of maternal toxicity; but a marked increase in maternal body weight was evident following dosing from GD14 to GD21. The maternal plasma profile following single subcutaneous dose of 50 mg/kg on both GD14 and GD21 showed a monoexponential elimination pattern. Statistically significant differences between treatments (GD14 versus GD21) were observed in elimination (k(el) = 0.12 versus 0.15 h(-1)), absorption (k(a) = 2.01 versus 3.14 h(-1)), maximum plasma concentration time points (T(max) = 1.49 versus 1.01 h); maximum plasma concentration (C(max) = 40.23 versus 36.31 microg/ml) and areas under the concentration-time curve (AUCs(0-infinity) = 421.88 versus 274 microg h/ml. Based on comparisons of C(max), T(max), and AUCs(0-infinity) between the actual data and single intraperitoneal (i.p.) data previously published, the s.c. administration exhibited slower disposition and higher absorbed amount. After multiple-dose administrations of 50 and 100 mg/kg every 12 h (07:00 and 19:00 h), steady-state plasma levels were lower than the computer prediction, and only slight accumulation was observed. In both dosing periods HEPP levels were similar in mothers and offspring at steady-state conditions. The high incidence of embryo death and reduced embryo weight at GD6-14 dosing compared to GD14-21 dosing suggest that embryos are more sensitive to the deleterious effects of HEPP than fetuses; however, the faster elimination observed at late gestation could also contribute to the lower toxicity observed during the fetal period. Because the maternal HEPP plasma levels and the AUC values were positively correlated with embryo/fetal toxicity end points, both pharmacokinetic parameters could be reliable indicators of offspring exposure and consequently of potential toxicity. These data suggest that the length of time that HEPP is present in the maternal plasma at a sufficiently high concentration could be determinant of adverse effects in the offspring. SN - 1091-5818 UR - https://www.unboundmedicine.com/medline/citation/17564905/Gestational_age_dependency_in_the_prenatal_toxicity_and_in_the_disposition_kinetics_of_the_novel_anticonvulsant_HEPP__DL_3_hydroxy_3_ethyl_3_phenylpropionamide__after_subcutaneous_administration_in_pregnant_rats_ L2 - http://journals.sagepub.com/doi/full/10.1080/10915810701352846?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub=pubmed DB - PRIME DP - Unbound Medicine ER -