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1.
J Dev Orig Health Dis ; 11(1): 7-17, 2020 02.
Artículo en Inglés | MEDLINE | ID: mdl-31138338

RESUMEN

BACKGROUND: Intrauterine undernutrition could impact offspring left ventricle (LV) afterload and arterial function. The changes observed in adulthood could differ depending on the arterial type, pathway and properties studied. Aim: To analyze whether undernutrition during early and mid-gestation is associated with changes in cardiovascular properties in adulthood. METHODS: Pregnant ewes were assigned to one of the two treatment groups: (1) standard nutritional offer (high pasture-allowance, HPA; n = 16) or (2) nutritional restriction (50-75% of control intake) from before conception until day 122 of gestation (≈85% term) (low pasture allowance, LPA; n = 17). When offspring reached adult life, cardiovascular parameters were assessed in conscious animals (applanation tonometry, vascular echography). MEASUREMENTS: Peripheral and aortic pressure, carotid and femoral arteries diameters, intima-media thickness and stiffness, blood flow, local and regional resistances and LV afterload were measured. Blood samples were collected. Parameters were compared before and after adjustment for nutritional characteristics at birth and at the time of the cardiovascular evaluation. RESULTS: Doppler-derived cerebral vascular resistances, mean pressure/flow ratio (carotid resistance) and afterload indexes were higher in descendants from LPA than in descendants from HPA ewes (p < 0.05). Descendants from LPA had lower femoral diameters (p < 0.05). Cardiovascular changes associated with nutritional restriction during pregnancy did not depend on the offsprings' nutritional conditions at birth and/or in adult life. CONCLUSION: Pregnant ewes that experienced undernutrition gave birth to female offspring that exhibited increased carotid pathway resistances (cerebral microcirculatory resistances) and LV afterload when they reached the age of 2.5 years. There were differences in the impact of nutritional deficiency on elastic and muscular arteries.


Asunto(s)
Enfermedades Cardiovasculares/etiología , Desnutrición/complicaciones , Fenómenos Fisiologicos Nutricionales Maternos , Efectos Tardíos de la Exposición Prenatal/etiología , Resistencia Vascular/fisiología , Animales , Enfermedades Cardiovasculares/fisiopatología , Arterias Carótidas/crecimiento & desarrollo , Arterias Carótidas/fisiopatología , Grosor Intima-Media Carotídeo , Modelos Animales de Enfermedad , Femenino , Factores de Riesgo de Enfermedad Cardiaca , Ventrículos Cardíacos/crecimiento & desarrollo , Ventrículos Cardíacos/fisiopatología , Humanos , Desnutrición/fisiopatología , Microcirculación/fisiología , Embarazo , Efectos Tardíos de la Exposición Prenatal/fisiopatología , Ovinos , Ultrasonografía Doppler
2.
Int J Mol Sci ; 20(14)2019 Jul 15.
Artículo en Inglés | MEDLINE | ID: mdl-31311132

RESUMEN

Cardiovascular risk associated with fetal growth restriction (FGR) could result from an early impaired vascular function. However, whether this effect results in premature vascular aging has not been addressed. We studied the ex vivo reactivity of carotid and femoral arteries in fetal (near term), adults (eight months-old) and aged (16 months-old) guinea pigs in normal (control) and FGR offspring. Additionally, an epigenetic marker of vascular aging (i.e., LINE-1 DNA methylation) was evaluated in human umbilical artery endothelial cells (HUAEC) from control and FGR subjects. Control guinea pig arteries showed an increased contractile response (KCl-induced) and a progressive impairment of NO-mediated relaxing responses as animals get older. FGR was associated with an initial preserved carotid artery reactivity as well as a later significant impairment in NO-mediated responses. Femoral arteries from FGR fetuses showed an increased contractility but a decreased relaxing response compared with control fetuses, and both responses were impaired in FGR-adults. Finally, FGR-HUAEC showed decreased LINE-1 DNA methylation compared with control-HUAEC. These data suggest that the aging of vascular function occurs by changes in NO-mediated responses, with limited alterations in contractile capacity. Further, these effects are accelerated and imposed at early stages of development in subjects exposed to a suboptimal intrauterine environment.


Asunto(s)
Envejecimiento/patología , Endotelio Vascular/crecimiento & desarrollo , Retardo del Crecimiento Fetal/patología , Animales , Arterias Carótidas/crecimiento & desarrollo , Arterias Carótidas/patología , Arterias Carótidas/fisiopatología , Células Cultivadas , Metilación de ADN , Endotelio Vascular/metabolismo , Endotelio Vascular/patología , Femenino , Arteria Femoral/crecimiento & desarrollo , Arteria Femoral/patología , Arteria Femoral/fisiopatología , Retardo del Crecimiento Fetal/genética , Cobayas , Humanos , Elementos de Nucleótido Esparcido Largo/genética , Óxido Nítrico/metabolismo , Vasoconstricción , Vasodilatación
3.
PLoS One ; 10(1): e0115166, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25611747

RESUMEN

OBJECTIVE: To examine the relationship between carotid intima-media thickness (IMT) at age 30 and birth characteristics, growth during infancy, and breastfeeding duration, among subjects who have been prospectively followed since birth. METHODS AND RESULTS: In 1982, all births in the city of Pelotas, southern Brazil, were identified and those children (n = 5,914) whose families lived in the urban area of the city have been followed and evaluated at several time points. The cohort participants were evaluated in 2012-13, and IMT was measured at the posterior wall of the right and left common carotid arteries in longitudinal planes using ultrasound imaging. We obtained valid IMT measurements for 3,188 individuals. Weight-for-age z-score (WAZ) at age 2 years, weight-for-height z-score (WHZ) at age 4, height-for-age z-score (HAZ) at 4 years, WAZ at age 4 and relative conditional weight at 4 years were positively associated with IMT, even after controlling for confounding variables. The beta-coefficient associated with ≥ 1 s.d. WAZ at age 2 (compared to those with a <-1 s.d.) was 3.62 µm (95% CI 0.86 to 6.38). The beta-coefficient associated with ≥ 1 s.d. WHZ at 4 (in relation to <-1 s.d) was 3.83 µm (95% CI 0.24 to 7.42). For HAZ at 4, the beta-coefficient for ≥ 1 s.d. in relation to <-1 s.d. was 4.19 µm (95% CI 1.14 to 7.25). For WAZ at 4, the beta-coefficient associated with ≥ 1 s.d. in relation to <-1 s.d. was 4.28 µm (95% CI 1.59 to 6.97). The beta-coefficient associated with conditional weight gain at age 2-4 was 1.26 µm (95% CI 0.49 to 2.02). CONCLUSION: IMT at age 30 was positively associated with WAZ at age 2 years, WHZ at age 4, HAZ at age 4, WAZ at age 4 and conditional weight gain at age 4 years.


Asunto(s)
Peso al Nacer , Lactancia Materna , Arterias Carótidas/anatomía & histología , Desarrollo Infantil , Túnica Íntima/anatomía & histología , Adulto , Brasil , Arterias Carótidas/crecimiento & desarrollo , Preescolar , Estudios de Cohortes , Femenino , Humanos , Recién Nacido , Masculino , Túnica Íntima/crecimiento & desarrollo
4.
Int. j. morphol ; 29(3): 927-929, Sept. 2011. ilus
Artículo en Inglés | LILACS | ID: lil-608683

RESUMEN

The maxillary artery (MA) is one of the terminal branches of the external carotid artery (ECA) and is located in the infratemporal fossa (IF). Some of the branches in this region are the inferior alveolar artery (IAA) and the buccal artery (BA), both descending branches. Here, we report an unusual unilateral origin of the IAA and the BA from a common trunk directly from the ECA. We conducted a routine dissection of both IF in a 54-year-old hispanic male cadaver. Fixed with Universidad de los Andes® conservative solution and red latex for vascular filling. On each side, the MA is observed superficially located over the lateral pterygoid muscle. On the right side, the IAA and the BA originate from a common trunk from the ECA approximately 5 mm prior to the bifurcation into their terminal branches. On the left side, the IAA originates from the MA that is immediately next to its origin, making a common trunk with the pterygoid branches. Knowing the morphology of the MA and its branches at the IF is important for oral and maxillofacial surgery procedures; and any variation in the origin or course of these arteries may result in the patient's increased morbidity during some invasive procedure in the area.


La arteria maxilar (AM) es una rama terminal de la arteria carótida externa (ACE), y se ubica en la región infratemporal (RI). Algunas de sus ramas en esta región son la arteria alveolar inferior (AAI) y la arteria bucal (AB), ambas ramas descendentes. En este trabajo informamos de un inusual origen unilateral de la AAI y de la AB a partir de un tronco común desde la ACE. Se realizó una disección de rutina de ambas regiones infratemporales en un cadáver de 54 años, sexo masculino, caucásico. Fijado con solución conservadora Universidad de los Andes® y repleción vascular con látex rojo. A cada lado, se observa la AM en ubicación superficial sobre el músculo pterigoideo lateral. Al lado derecho, la AAI y la AB se originan de un tronco común desde la ACE aproximadamente 5 mm antes de la bifurcación en sus ramas terminales. Al lado izquierdo la AAI se origina de la AM inmediato a su origen, formando un tronco común con los ramos pterigoideos. El conocimiento de la morfología de la AM y de sus ramas en la RI es de importancia en procedimientos odontológicos, de cirugía oral y maxilofacial. Por lo que cualquier variación en el origen o trayecto de estas arterias puede predisponer a un paciente a una mayor morbilidad durante algún procedimiento invasivo en la zona.


Asunto(s)
Persona de Mediana Edad , Alveolo Dental/irrigación sanguínea , Arteria Maxilar/anatomía & histología , Arteria Maxilar/anomalías , Arteria Maxilar/crecimiento & desarrollo , Arteria Maxilar/embriología , Arterias Carótidas/anatomía & histología , Arterias Carótidas/crecimiento & desarrollo , Arterias Carótidas/embriología , Arterias Carótidas/ultraestructura , Boca/irrigación sanguínea , Arterias Temporales/anatomía & histología , Arterias Temporales/crecimiento & desarrollo , Hueso Temporal/irrigación sanguínea
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