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In utero programming of adult vascular function in transgenic mice lacking low-density lipoprotein receptor.| Autores: | Josje Langenveld, Fanxian Lu, Egle Bytautiene, Garland D Anderson, George R Saade, Monica Longo | | Idioma: | ENG. | | Fecha: | 24-3-2008 | | Revista: | American journal of obstetrics and gynecology
(1097-6868)
| | Entrega: | Am J Obstet Gynecol. 21 Mar 2008 | |
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Abstract:
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OBJECTIVE:
The objective of this study was to examine the role of maternal hypercholesterolemia in fetal programming of adult vascular function using transgenic mice lacking the low-density lipoprotein receptor (LDLR).
STUDY
DESIGN:
Homozygous LDLR knockout mice (B6.129S7-Ldlr(tm1Her)/J, LDLR(-/-KO)) and their wild-type controls (C57BL/6J, LDLR(+/+WT)) were cross-bred to produce 4 litter groups: LDLR(-/-KO), maternally derived heterozygous (LDLR(+/-Mat)), paternally derived heterozygous (LDLR(+/-Pat)) and LDLR(+/+WT). Female and male offspring were killed at 10-12 weeks of age, and carotid arteries were used for in vitro experiments.
RESULTS:
The dose responses to phenylephrine were significantly higher in LDLR(-/-KO) and LDLR(+/-Mat) male offspring. The contractile responses to phenylephrine in female mice were significantly increased only in the LDLR(-/-KO) offspring. Maximal Ca(2+) contraction was higher in LDLR(-/-KO) male and female offspring.
CONCLUSION:
Despite being genomically similar, heterozygous offspring that developed in a hypercholesterolemic maternal environment had abnormal vascular responses later in life compared with those that developed in a normal environment.
| | Copyright: | American journal of obstetrics and gynecology
Department of Obstetrics and Gynecology, Máxima Medical Centre, Veldhoven, The Netherlands. | | Full text: | | | |
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Artículos de otras especialidades: Aparato Digestivo, Hematología, Cirugía Plástica, Geriatria, Neurofisiología Clínica, Obstetricia y Ginecología, Medicina Preventiva, Rehabilitación, Anatomía Patológica, Medicina de Urgencias, Cirugía General - Ap. Digestivo, Endocrinología |
