1.The reliability of serum myelin basic protein and S100B protein in predicting outcome of premature infants with periventricular leukomalacia
Runzhong HUANG ; Jianwei HUANG ; Xiaoyang WENG ; Jinfeng ZHANG ; Liuquan PENG ; Yongmian SU ; Ya NIE
Chinese Pediatric Emergency Medicine 2011;18(6):533-535
Objective To investigate the changes of serum myelin basic protein (MBP) and S100B orotein (S100B) in premature infants with periventricular leukomalacia (PVL) and their outcomes.Methods Seventy-eight premature infants with PVL (PVL group)and 43 normal infants (control group)who were hospitalized in our hospital from Nov 2007 to Jul 2008 were enrolled in the study.The infants were sampled for MBP and S100B levels on 1st,3rd,7th and 14th d after birth.Thirty normal infants and 69 infants with PVL were followed up every three months as they discharged until they were one year corrected age and their development quotients(DQ) were measured using Gesell development schedules.Results ( 1 ) The serum MBP levels increased on day 1 [ (7.61 ± 1.78 ) μg/L ],peak on day 3 [ ( 14.53 ± 3.12 ) μg/L],and then decreased.The serum MBP levels in infants with PVL group were significantly higher than those of control group at 1st,3rd,7th and 14th d after birth ( P < 0.05 ).(2) The serum S100B levels increased on day 1,day 3 and day 7 [ (3.82 ±0.68),(4.41 ±0.91,),(5.78 ± 1.54) μg/L],peaked on day 7,and then decreased.The S100B levels of infants in PVL group were significantly higher than those of control group at 1st,3rd and 7th d after birth (P <0.05) ;and decreased on day 14 (P>0.05).(3) Infants whose MBP and S100B levels increased at 7th day after birth had significantly decreased DQ than those of normal infants ( P <0.05 ).Conclusion The serum MBP and S100B levels in infants with PVL are correlated with the severity of central nervous system injury.If the serum S100B and MBP levels of PVL infants continues to rise more than 7 d,the DQ are lower,and the outcomes are poor.
2.Experimental studies on toxic effects of Tiangou Jiangya capsule.
Ying CHEN ; Yujie LI ; Qing YANG ; Xiaoyang WENG ; Lijuan ZOU ; Xiaoxin ZHU
China Journal of Chinese Materia Medica 2011;36(23):3358-3363
OBJECTIVETo study the acute and chronic toxicity of Tiangou Jiangya capsule.
METHODTiangou Jiangya capsule was intragastrically administered to mice twice a day. The appearance, behavior, mental status, respiratory changes of mice and the number of poisoned and dead mice in each group were noted daily for 14 consecutive days. The amount of weight and feed of survived mice were recorded every day. The mice were divided into four groups: the treatment groups (minimum, middle, maximum dose of Tiangou Jiangya capsule) and the control group. After continuously orally administrated for 6 months, the rats' behavior, weight gain, food consumption, indications for hematology, blood biochemistry, urine analysis, electrocardiogram, systematic autopsy and histopathology were observed. The above physiological indexes were inspected again 1 month after cease of administration.
RESULTThe oral acute toxicity study of Tiangou Jiangya capsule in mice revealed that the maximum dose is 534.86 g x kg(-1), which was 534.86 times the recommended human maximum dose in clinical practice. Compared with normal control group, no significant differences were observed in rats' behaviors, food-intake, electrocardiogram and relative examination indexes among the treatment groups. There was no difference of hematology, biochemistry test, urine and histopathology.
CONCLUSIONThe minimum dosage of Tiangou Jiangya capsule is relatively safe. It caused weight loss by administrated with the middle and maximum dose for 6 months, which should be paid attention in clinical studies.
Animals ; Antihypertensive Agents ; administration & dosage ; toxicity ; Behavior, Animal ; drug effects ; Benzyl Alcohols ; administration & dosage ; toxicity ; Body Weight ; drug effects ; Drugs, Chinese Herbal ; administration & dosage ; toxicity ; Eating ; drug effects ; Electrocardiography ; drug effects ; Female ; Flavonoids ; administration & dosage ; toxicity ; Furans ; administration & dosage ; toxicity ; Glucosides ; administration & dosage ; toxicity ; Lignans ; administration & dosage ; toxicity ; Male ; Mice ; Mice, Inbred ICR ; Rats ; Rats, Wistar