Browsing by Author "Dourado, Vitor Alves"

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    Cigarette smoke causes changes in liver and spleen of mice newborn exposed during pregnancy.
    (2013) Diniz, Mirla Fiuza; Dourado, Vitor Alves; Silva, Marcelo Eustáquio; Pedrosa, Maria Lúcia; Bezerra, Frank Silva; Lima, Wanderson Geraldo de
    Cigarette smoking can lead to pivotal morphological changes in several human and animal tissues, especially when the exposure occurs during neonatal life. We evaluated the livers and spleens of C57BL/6 neonatal mice to determine possible morphological changes induced by exposure to cigarette smoke. In total, 15 C57BL/6 adult mice were used for mating, placing 2 female mice per male mouse for a 5-day period. Pregnant female mice were divided into 2 groups: the first group (ICS21) consisted of 5 female mice that were exposed to 4 cigarettes, 3 times daily for 21 days. They were subjected to 6 min of exposure per cigarette in an inhalation chamber. The second group (CG) consisted of 5 female mice that were not exposed to cigarette smoking and was used as a control group. Seven neonatal mice from both groups were weighed 24 h post-birth and then euthanized. Their livers and spleens were weighed and fixed for routine histological processing. Morphometric analysis was used to assess possible hepatic inflammation, measure hepatic glycogen and collagen deposition areas. Total spleen area, white pulp, and red pulp were identified. A reduction in body weight was observed in ICS21 mice as compared to CG mice, and a similar trend was observed in the liver and spleen weights. Histological analysis indicated the presence of more number of inflammatory cells in the ICS21 livers than that in the CG livers. Moreover, smaller hepatic glycogen deposition areas were observed in ICS21 mice than that in CG mice. However, no difference in hepatic collagen deposition was observed between the 2 groups. No differences were observed in the areas of the total organ and the white and red pulp areas between the 2 groups. However, the proportion of the white pulp and total area was lower in the ICS21 spleens than that in the CG spleens. Our results indicate that exposure to cigarette smoke during neonatal life can induce changes in fetal tissues, which translate to several changes in the organs of the neonatal mice.
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    Exposure to cigarette smoke during pregnancy causes redox imbalance and histological damage in lung tissue of neonatal mice.
    (2014) Campos, Keila Karine Duarte; Dourado, Vitor Alves; Diniz, Mirla Fiuza; Bezerra, Frank Silva; Lima, Wanderson Geraldo de
    Smoking during pregnancy is directly associated with numerous serious conditions, such as premature birth, low birth weight, and perinatal mortality. We quantitatively evaluated histological inflammatory alterations, oxidative damage by lipid peroxidation, the activity of the antioxidant enzymes superoxide dismutase (SOD) and catalase (CAT) in the lungs of mice exposed to cigarette smoke during pregnancy. Eight female and four male mice were mated for five days. Pregnant female mice were randomly allocated to the control group or to the cigarette smoke group (n = 8) in which they were exposed to 12 cigarettes per day in an exposure chamber, three times a day for 21 days. The control group (CG; n = 8) was kept in the exposure chamber for the same duration, but without exposure to cigarette smoke. Six newborn mice from both groups were weighed 24 hours after birth and then euthanized. Lung tissue was collected and subjected to histomorphometric and biochemical analyses. The cigarette smoke group showed a significant reduction in snout-vent length compared to the control group. Histomorphometric analysis indicated increased alveolar septal thickness and a larger alveolar lumen in mice exposed to cigarette smoke than in mice in the control group. We observed increased alveolar inflammatory infiltrate, decreased SOD activity, and significantly higher oxidative damage in the cigarette smoke group. Our data indicate that cigarette smoke exposure during pregnancy decreases body length at birth, changes lung tissue, and causes redox imbalance and histological damage in newborn mice.