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1.
Behav Brain Res ; 451: 114526, 2023 08 05.
Artículo en Inglés | MEDLINE | ID: mdl-37271313

RESUMEN

This study aimed to evaluate the behavioral and energy metabolism parameters in female mice subjected to obesity and offspring deprivation (OD) stress. Eighty female Swiss mice, 40 days old, were weighed and divided into two groups: Control group (control diet, n = 40) and Obese group (high-fat diet, n = 40), for induction of the animal model of obesity, the protocol was based on the consumption of a high-fat diet and lasted 8 weeks. Subsequently, the females were subjected to pregnancy, after the birth of the offspring, were divided again into the following groups (n = 20): Control non-deprived (ND), Control + OD, Obese ND, and Obese + OD, for induction of the stress protocol by OD. After the offspring were 21 days old, weaning was performed and the dams were subjected to behavioral tests. The animals were humanely sacrificed, the brain was removed, and brain structures were isolated to assess energy metabolism. Both obesity and OD led to anhedonia in the dams. It was shown that the structures most affected by obesity and OD are the hypothalamus and hippocampus, as evidenced by the mitochondrial dysfunction found in these structures. When analyzing the groups separately, it was observed that OD led to more pronounced mitochondrial damage; however, the association of obesity with OD, as well as obesity alone, also generated damage. Thus, it is concluded that obesity and OD lead to anhedonia in animals and to mitochondrial dysfunction in the hypothalamus and hippocampus, which may lead to losses in feeding control and cognition of the dams.


Asunto(s)
Anhedonia , Efectos Tardíos de la Exposición Prenatal , Embarazo , Ratones , Femenino , Animales , Humanos , Obesidad/metabolismo , Dieta Alta en Grasa/efectos adversos , Destete , Metabolismo Energético
2.
An Acad Bras Cienc ; 92(4): e20200837, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-33295581

RESUMEN

The intrauterine environment is infl uenced by several factors, genetic or environmental, which are essential in understanding the pathophysiological mechanisms of some diseases. In this study, the aim was to investigate the impact of prenatal lipopolysaccharide exposure on the development of rats. Fifty pregnant rats received intraperitoneal administration of lipopolysaccharide (100 µg/kg), or saline at the same dose, on the 9.5th day of pregnancy. The offspring of these rats were analyzed for indicators of brain and somatic development and maturation of physical characteristics. Refl ex ontogenesis was also analyzed by vibrissae placement, negative geotaxis, palmar grasp, precipice aversion, decubitus recovery and acceleration reaction. Administration of lipopolysaccharide on the 9.5th gestational day caused delayed opening of the auditory pavilion, reduction in the length of the tail, body, cranial axes, and body weight. Thus, maternal infections can interfere in the intrauterine environment, impairing functional and structural aspects of the central nervous system, as well as the maturation of physical characteristics.


Asunto(s)
Lipopolisacáridos , Efectos Tardíos de la Exposición Prenatal , Factores de Edad , Animales , Animales Recién Nacidos , Conducta Animal , Peso Corporal , Femenino , Lipopolisacáridos/toxicidad , Embarazo , Ratas , Cola (estructura animal)
3.
Molecules ; 17(9): 10331-43, 2012 Aug 29.
Artículo en Inglés | MEDLINE | ID: mdl-22932214

RESUMEN

A series of new chalcones substituted with azide/triazole groups were designed and synthesized, and their cytotoxic activity was evaluated in vitro against the HeLa cell line. O-Alkylation, Claisen-Schmidt condensation and Cu(I)-catalyzed cycloaddition of azides with terminal alkynes were applied in key steps. Fifteen compounds were tested against HeLa cells. Compound 8c was the most active molecule, with an IC50 value of 13.03 µM, similar to the value of cisplatin (7.37 µM).


Asunto(s)
Azidas/química , Muerte Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Chalconas/síntesis química , Chalconas/farmacología , Triazoles/química , Alquilación/efectos de los fármacos , Catálisis , Línea Celular Tumoral , Chalconas/química , Reacción de Cicloadición , Diseño de Fármacos , Femenino , Células HeLa , Humanos , Concentración 50 Inhibidora , Estructura Molecular
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