Observation and measurement of silicosis animal model by PET-CT
10.11763/j.issn.2095-2619.2017.03.001
- Author:
Ming HUANG
1
,
2
;
Yingxun ZHANG
1
,
2
;
Fengrong LU
1
,
2
;
Xiangrong SONG
1
,
2
;
Ling YAN
1
,
2
;
Ruiwen LI
1
,
2
;
Yongshun HUANG
1
,
2
;
Xiaojing ZENG
1
,
2
;
Hanlin HUANG
1
,
2
Author Information
1. Guangdong Province Hospital for Occupational Disease Prevention and Treatment
2. Guangdong Provincial Key Laboratory of Occupational Disease Prevention and Treatment Guangzhou,Guangdong 510300,China
- Publication Type:Journal Article
- Keywords:
Silicosis;
Animal models;
Positron emission tomography;
Computed tomography;
Standardized uptake value;
Rat
- From:
China Occupational Medicine
2017;44(03):245-252
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE: To explore the feasibility of dynamic observation and measurement of living silicosis rat model by using small animal positron emission tomography( PET)-computed tomography( CT). METHODS: Specific pathogens free SD rats were divided into model group and control group. The silicosis rat model was established by one-time endotracheal injection of 30 g/L silica suspension,while the control group rats were injected of isopyknic 0. 9% sodium chloride solution. Six rats from each group were randomly selected for CT scan from 1st,2nd,3rd,4th,6th,8th and 12 th week after silica injection using the small animal PET-CT. CT value and standardized uptake value( SUV) of18F-fluorodeoxyglucose were measured. Lung tissue was collected for pathological sections. The levels of hydroxyproline( HYP) of lung tissue and serum transforming growth factor β1( TGF-β1) and interleukin-1( IL-1) were measured.RESULTS: Pathological sections of rats of model group showed inflammatory exudation,inflammation reduced and fibrosis increased with extended time. The results are identical with findings in PET-CT. Lung SUV of rats in model group in the1st-3rd weeks were higher than that in control group in the same time point( P < 0. 05) and decreased by the increasing time during the 1st-4 th weeks of dust injection( P < 0. 05). Lung CT values of model group in the 1st-12 th weeks were higher than that of control group in the same 7 time points( P < 0. 05) and decreased in the 1st-6th weeks and then increased in the 6th-12th weeks by the increasing time of dust injection( P < 0. 05). Lung coefficients and HYP levels of model group in the 7 time points were higher than that of control group in the same 7 time points( P < 0. 05). Lung coefficients decreased in 1st-4th weeks and lung HYP levels increased in 6th-12th weeks with the increasing time of dust injection( P < 0. 05). Excepted of the 3rd and 4th weeks,serum TGF-β1 levels of model group in other 5 time-points were higher than that of control group in the same 5 time points( P < 0. 05) and decreased in the 1st-4th weeks( P < 0. 05)then increased in the 4th-8th weeks( P < 0. 05) by the increasing time of dust injection. Serum IL-1 levels of model group in the 1st-4th weeks were higher than that of control group in the same 4 time points( P < 0. 05) and decreased by the increasing time of dust injection( P < 0. 05) and decreased by the increasing time of dust injection( P < 0. 05).CONCLUSION: Early inflammation and terminal fibrosis of living silicosis rat model could be observed effectively by small animal PET-CT,which can be used as a new approach for dynamic tracing silicosis in rat models.
