2.Effect of methylprednisolone on bone mass, microarchitecture and microdamage in cortical bone of ulna in rats.
Yuhai ZHANG ; Ruchun DAI ; Jie XIAO ; Daoxiong CHEN ; Eryuan LIAO
Journal of Central South University(Medical Sciences) 2015;40(1):25-30
OBJECTIVE:
To explore the effect of methylprednisolone on bone mass, microarchitecture and microdamage in cortical bone of ulna in rats.
METHODS:
Twenty female Sprague-Dawley rats (3.5 months old) were randomly assigned to two groups: a treatment group and a control group (n=10 per group). The treatment group was subcutaneously injected with methylprednisolone 3.5 mg/(kg.d) while the control group was subcutaneously injected with same volume of vehicle (saline). Rats were sacrificed at 9 weeks after the treatments. Before the sacrifice, the body weight and total bone mineral density (BMD) were measured. The right forelimb was separated through humeral shoulder and then single axial fatigue loading was performed on the right ulna. After fatigue load, the middle ulna section was bulkstained in basic fuchsin. Bone histomorphometry and microdamage analysis were performed on the middle ulna section.
RESULTS:
Compared with the control group, the body weight, total bone BMD and ulnas BMD in the treatment group were decreased by 15%, 6.4% and 4.3% respectively (all P<0.05); the ulna inner perimeter and marrow area in the treatment group were increased by 23.3% and 32%, respectively (both P<0.05), while the outer perimeter were decreased by 3.1% (P>0.05). There was no significant difference in the cortical and total area between the 2 groups (both P>0.05). The number of microcrack, microcrack density and microcrack surface density in the treatment group were increased by 43%, 48% and 50%, respectively, compared with those in the control group (all P<0.05), but there was no significant difference in the mean length of microcrack between the 2 groups (P>0.05).
CONCLUSION
Methylprednisolone can significantly induce the bone loss and the deterioration of microarchitecture and microdamage in ulna of rats.
Animals
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Bone Density
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drug effects
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Female
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Methylprednisolone
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pharmacology
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Rats
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Rats, Sprague-Dawley
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Ulna
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drug effects
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pathology
3.Diagnosis and prevention of fungal infection in severe acute pancreatitis
Yueming HE ; Xinsheng L ; Zhongli AI ; Zhisu LIU ; Daoxiong LEI ; Boyong WANG ; Qun QIAN ; Quan SUN ; Jiwei CHEN ; Xinyuan OU ; Jun XU ; Congqing JIANG ; Yufeng YUAN ; Jun CAO
Chinese Journal of General Surgery 1997;0(06):-
ObjectiveTo study the early diagnosis and prevention of fungal infection in severe acute pancreatitis(SAP). Method 1.SAP patients from July 1998 to June 2002 were prospectively randomized into 3 groups: garlicin prevention group, fluconazole (low dosage) prevention group and control group, the incidence of fungal infection in SAP was compared between the groups. For fungal infection patients, the fungal clearance and mortality rate were observed. 2.Clinical data of SAP patients with fungal infection and with simple bacterial infection was compared by multivariate logistic regression, and clinical characters and risk factors of fungal infection were evaluated. Results 1.There were lower incidences of fungal infection in garlicin group (16% vs. 30%,P
4.Prevention and therapy of fungal infection in patients with severe acute pancreatitis
Yueming HE ; Xinsheng LU ; Zhongli AI ; Zhisu LIU ; Daoxiong LEI ; Boyong WANG ; Qun QIAN ; Quan SUN ; Jiwei CHEN ; Xinyuan OU ; Rui XU ; Congqing JIANG ; Yufeng YUAN ; Jun CAO
Chinese Journal of General Surgery 1993;0(02):-
Objective To determine the prevention and therapy of fungal infection in patients with severe acute pancreatitis (SAP). Methods Seventy patients with SAP admitted from July,1998 to June,2002 were randomly divided into 3 groups: garlicin prevention group, fluconazole (low dosage) prevention group and control group.The incidence of fungal infection, the fungal clearance and mortality after the treatment were compared. Results The incidence of fungal infection in garlicin group and fluconazole group was lower than that in control group. (16%∶30%,P
5.Influence of anastomotic leakage on long-term survival after resection for rectal cancer.
Hailin KE ; Pan CHI ; Huiming LIN ; Xingrong LU ; Ying HUANG ; Zongbin XU ; Shenghui HUANG ; Zhifen CHEN ; Yanwu SUN ; Daoxiong YE ; Xiaojie WANG
Chinese Journal of Gastrointestinal Surgery 2015;18(9):920-924
OBJECTIVETo investigate the influence of anastomotic leakage (AL) on long-term survival after resection for rectal cancer.
METHODSClinicopathological data of 653 rectal cancer cases confirmed by pathology and undergoing R0 resection for rectal cancer in our department from January 2007 to December 2011 were retrospectively analyzed. Anastomotic leakage was found in 40 cases (AL group) and not in the other 613 cases (non-AL group). After median 47 (1-91) months of follow-up, 5-year disease-free survival rate, distant metastasis rate and local recurrence rate were compared between the two groups. Risk factors affecting long-term prognosis were also analyzed.
RESULTSThe 5-year disease-free survival rate, 5-year distant metastasis rate, and 5-year local recurrence rate were 78.1%, 14.2% and 4.2% in the non-AL group, and 74.5%, 20.1% and 8.4% in the AL group respectively, and the differences were not statistically significant (P=0.808, P=0.965, P=0.309). Multivariate analysis showed that preoperative neoadjuvant radiochemotherapy, TNM staging, abnormal CA199, preoperative low level of albumin were independent prognostic factors of rectal cancer patients after R0 resection, while AL was not an independent factor of 5-year disease-free survival (P=0.910). Further multivariate analysis on 507 cases receiving postoperative adjuvant chemotherapy also revealed that AL was not an independent factor of 5-year disease-free survival (P>0.05). Percentage difference of patients finishing postoperative chemotherapy between the two groups was not statistically significant (79.4% vs. 76.3%, P=0.681).
CONCLUSIONAL is not an independent predictor of long-term survival for rectal cancer.
Anastomotic Leak ; Chemotherapy, Adjuvant ; Disease-Free Survival ; Humans ; Neoadjuvant Therapy ; Neoplasm Recurrence, Local ; Neoplasm Staging ; Postoperative Period ; Prognosis ; Rectal Neoplasms ; pathology ; Retrospective Studies ; Survival Rate