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1.
Chinese Journal of Contemporary Pediatrics ; (12): 1045-1050, 2014.
Article Dans Chinois | WPRIM | ID: wpr-289537

Résumé

<p><b>OBJECTIVE</b>To observe the long-term changes in anxiety-like behavior and tyrosine hydroxylase (TH) expression in the substantia nigra (SN) after hypoxic-ischemic brain damage (HIBD) in a neonatal rat model and to further explore the relationship between dopamine (DA) level and long-term anxiety-like behavior using the DA receptor (DAR) antagonist.</p><p><b>METHODS</b>Seven-day-old (P7) neonatal Sprague-Dawley (SD) rats were randomized into normal control, sham-operated, HIBD and HIBD+DAR antagonist groups. HIBD model was prepared by ligating the right common carotid artery and 8% hypoxia exposure. The rats in the sham-operated group were sham-operated and were not subjected to right common carotid artery ligation and hypoxia exposure. The DAR antagonist was injected intraperitoneally before and after inducing HIBD. The same amount of normal saline was given to the other three groups as a control. Anxiety-like behavior was evaluated by elevated plus maze test, and TH expression in the SN was measured by immunohistochemistry on P14, P21, and P28.</p><p><b>RESULTS</b>On P21 and P28, the time spent in the open arms and the percentage of open arms entries in the HIBD group were significantly increased compared with those in the normal control, sham-operated and HIBD+DAR antagonist groups (P<0.05); in addition, the HIBD+DAR antagonist group showed a significantly longer time spent in the open arms than the normal control group (P<0.05). On P14, P21, and P28, TH expression in the HIBD and HIBD+DAR antagonist groups was significantly lower than that in the normal control and sham-operated groups, and TH level in the HIBD group was significantly lower than that in the HIBD+DAR antagonist group (P<0.05).</p><p><b>CONCLUSIONS</b>DAR antagonist allows the restoration of anxiety-like behavior and alleviates the damage to dopaminergic neurons in SD rats after HIBD.</p>


Sujets)
Animaux , Rats , Animaux nouveau-nés , Anxiété , Antagonistes de la dopamine , Utilisations thérapeutiques , Hypoxie-ischémie du cerveau , Apprentissage du labyrinthe , Rat Sprague-Dawley , Récepteurs dopaminergiques , Physiologie , Substantia nigra , Tyrosine 3-monooxygenase
2.
Chinese Journal of Pediatrics ; (12): 336-339, 2013.
Article Dans Chinois | WPRIM | ID: wpr-359742

Résumé

<p><b>OBJECTIVE</b>To quantitatively assess the association between transfusions and the risk of necrotizing enterocolitis (NEC) in neonates.</p><p><b>METHOD</b>Both Chinese and English literature published from Jan. 1985 to Nov. 2011 about the case-control study of the association between transfusions and neonatal NEC were retrieved by searching the electronic resource databases. A meta-analysis was then performed on the comparison and synthesis of findings from included studies. Pooled odds ratio (OR) and 95% confidence interval (CI) were calculated using RevMan 5.0 software. Sensitivity analysis was conducted and possible publication bias was tested as well.</p><p><b>RESULT</b>A total of 7 case-control studies (480 blood transfusion cases, 2845 control cases) were included. The meta-analysis with a random-effects model found a pooled OR of 3.35 (95% CI: 1.54-7.27). Sensitivity analysis showed that OR for post-transfusion NEC within 48 h was 4.21 (95% CI: 2.17-8.16). The OR was 4.29 (95% CI: 1.39-13.24) after factors such as gestational age and birth weight were de-confounded. The fail-safe number was 263.</p><p><b>CONCLUSION</b>Blood transfusion can increase the risk of NEC in neonates. The clinical application of this conclusion should be cautious due to limited reports. High-quality randomized control trials are still needed for the further proof of the association between blood transfusion and neonatal NEC.</p>


Sujets)
Femelle , Humains , Nouveau-né , Mâle , Biais (épidémiologie) , Études cas-témoins , Entérocolite nécrosante , Épidémiologie , Maladies néonatales , Épidémiologie , Thérapeutique , Prématuré , , Odds ratio , Facteurs de risque , Réaction transfusionnelle
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