1.Effect of deafferentation on parvalbumin of adult rat olfactory bulb.
Zhao-ping QIN ; Shu-ming YE ; Ji-zeng DU
Chinese Journal of Applied Physiology 2005;21(1):114-116
Afferent Pathways
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Animals
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Female
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Nerve Block
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Olfactory Bulb
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metabolism
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Parvalbumins
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metabolism
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Rats
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Rats, Wistar
2.Hypoxia change the gene expression of insulin-like growth factors family in rat prefrontal cortex.
Hu-Yue ZU ; Zhuan QU ; Ji-Long REN ; Xue-Qun CHEN ; Ji-Zeng DU
Chinese Journal of Applied Physiology 2014;30(1):30-32
Animals
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Gene Expression
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Hypoxia
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metabolism
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Prefrontal Cortex
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metabolism
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Rats
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Somatomedins
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metabolism
6.The response of hypothalamic CRF and AVP neurons of neonatal rats to simulated acute hypoxia.
Chinese Journal of Applied Physiology 2005;21(4):419-422
AIMTo investigate the response of hypothalamic corticotropin releasing factor (CRF) and arginine vasopressin (AVP) of adrenalectomized neonatal rats to hypoxia.
METHODSThe hypoxia was simulated in hypobaric cabin. The amount of arginine vasopressin (AVP) and corticotropin releasing factor (CRF) was assayed by RIA method.
RESULTSWhen neonatal rats exposed to acute hypoxia (simulated altitude of 5 000 m and 7 000 m, 24 h), their hypothalamic CRF was not changed in 3 d and 7 d rats, lower than control in 14 d, 21 d and 28 d rats, while hypothalamic AVP had no change in 3 d rats, was lower than control in 14 d and higher in 7 d, 21 d and 28 d rats. The responsive pattern of those two neuropeptides to acute hypoxia changed with the growth of rats. Adrenalectomy reduced the amount of hypothalamic CRF and AVP in 14 d, 21 d and 28 d rats, except AVP in 28 d rats. When adrenalectomized neonates exposed to hypoxia, there was no further change in CRF and AVE, means adrenalectomy not only removed the negative regulation of corticosteroid on CRF and AVE, but also inhibited the normal development of CRF and AVP neurons and thus, their responsive ability to hypoxia.
Animals ; Animals, Newborn ; Arginine Vasopressin ; metabolism ; Corticotropin-Releasing Hormone ; metabolism ; Hypothalamus ; cytology ; metabolism ; Hypoxia ; Neurons ; metabolism ; Rats ; Rats, Wistar ; Stress, Physiological
7.The effects of simulated hypoxia on the development of hypothalamic CRF and AVP neurons in postnatal rats.
Chinese Journal of Applied Physiology 2005;21(2):153-155
AIMTo investigate the influence of hypoxia on postnatal developing pattern of hypothalamic corticotropin releasing factor(CRF) and arginine vasopressin (AVP) in male and female neonatal rats.
METHODSThe hypoxia was simulated in hypobaric cabin. The content of AVP and CRF was assayed by RIA method.
RESULTSIt was showed the female rats had the similar developing process with male rats, either at 2300 m or at 5000 m altitude. When they developed at simulated 5000 m altitude, the content of their hypothalamic CRF was lower than that of control rats on postnatal day 21, while the content of AVP was higher than control on day 21 and 28.
CONCLUSIONMaybe the difference of the function between hypothalamic CRF and AVP or/and the incoherence of their developing stage contribute to their particular developing pattern at 5000 m altitude.
Altitude ; Animals ; Animals, Newborn ; Arginine Vasopressin ; metabolism ; Corticotropin-Releasing Hormone ; metabolism ; Female ; Hypothalamus ; metabolism ; Hypoxia ; Male ; Rats ; Rats, Wistar
8.Retrospective analysis on healthcare-associated infection in a cancer hospi-tal between 2006 and 2012
Xuesong FU ; Huimin ZENG ; Ji ZHANG ; Yunfeng YAO ; Li ZHANG ; Fengxin YANG ; Yunxia DU
Chinese Journal of Infection Control 2015;(10):704-707
Objective To investigate healthcare-associated infection(HAI)in patients in a cancer hospital,provide reference for controlling HAI in cancer patients,and guide rational use of antimicrobial agents.Methods Clinical data of patients in a cancer hospital between August 2006 and July 2012 were analyzed retrospectively.Results The incidence of HAI case was 1 .53% (2 060/134 389),and annual incidence showed a downward trend.The main in-fection site was lower respiratory tract (46.46%,n=957),followed by bloodstream (15.63%,n=322),abdominal and pelvic (14.03%,n=289).The main pathogens were Pseudomonas aeruginosa (16.16%,n=350),Staphylo-coccus aureus (9.97%,n=216),Klebsiella pneumoniae (9.79%,n=212),Escherichia coli (9.65%,n=209), and Candida albicans (6.51 %,n=141 ).Gram-negative bacilli,including Klebsiella pneumoniae and Escherichia coli ,were sensitive to carbapenems and β-lactamase inhibitors.Conclusion Lower respiratory tract is the major HAI site in patients with cancer,and gram-negative bacteria are the main pathogens.Carbapenems andβ-lactamase inhibitors are recommended for the empirical treatment of HAI in cancer patients.
10.Intermittent hypoxia influence lymphocyte proliferation of rats.
Jian-fen XU ; Xue-qun CHEN ; Ji-zeng DU
Chinese Journal of Applied Physiology 2005;21(1):5-8
AIMTo investigate intermittent hypoxia effects on splenocyte mitogen-induced proliferation.
METHODSRats were exposured to intermittent hypoxia in a hypobaric chamber 4 h/d for 1 d, 2 d, 5 d and 15 d.
RESULTS5 km (10.8% O2) hypoxia for 1 d significantly inhibited ConA-induced splenocytes proliferation by--74.57% +/- 7.33% (P < 0.05). Hypoxia (5 km) for 2 d, 5 d and 15 d did not markedly affect splenocyte proliferation (97.03 +/- 7.18%, 104.5% +/- 8.38%, 99.55% +/- 3.8% respectively). Hypoxia 2 km (16.0% O2) for 1 d, 2 d, 5 d and 15 d had no influence on splenocytes proliferation (93.19% +/- 11.88%, 96.43% +/- 7.9%, 99.03% +/- 10.97%, 100.54% +/- 9.54% respectively). We also demonstrated that acute hypoxia exposure (5 km) 4 h significantly suppressed DNA contents of rat splenocytes by 76.22% +/- 7.06% (P < 0.05). The suppressed DNA synthesis were returned to control level after the hypoxia for 5 d and 15 d.
CONCLUSIONThese results suggest that the acute hypoxia (5 km, 4 h) induces a transient suppression on splenic lymphocyte proliferation, and the intermittent hypoxia may induce an adaptation response of the splenocytes proliferation.
Animals ; Cell Proliferation ; Hypoxia ; immunology ; Lymphocyte Activation ; Lymphocytes ; cytology ; immunology ; Male ; Rats ; Rats, Sprague-Dawley ; Spleen ; immunology