Study on the difference of curative effect of conventional mercury displacement treatment on mercury in brain and kidney.
10.3760/cma.j.cn121094-20210202-00073
- Author:
Zhen Zhen GAO
1
,
2
;
Yu Jie PAN
3
;
Jing MA
3
;
Hui Ling LI
3
;
Xue MEI
1
,
2
;
Yu Guo SONG
3
Author Information
1. Emergency medical research center of Beijing Chaoyang Hospital Affiliated to Capital Medical University
2. Beijing Key Laboratory of Cardiopulmonary Resuscitation, Beijing 100020, China.
3. Department of Occupational Disease and Poisoning Medicine, Beijing Chaoyang Hospital Affiliated to Capital Medical University, Beijing 100020, China.
- Publication Type:Journal Article
- Keywords:
Brain;
Kidney;
Mercury poisoning;
Mercury treatment;
Rats
- MeSH:
Animals;
Brain/drug effects*;
Glutathione;
Inflammation;
Kidney/drug effects*;
Kidney Diseases/chemically induced*;
Male;
Mercuric Chloride/therapeutic use*;
Mercury/urine*;
Mercury Poisoning/drug therapy*;
Rats;
Rats, Sprague-Dawley;
Saline Solution/therapeutic use*;
Unithiol/therapeutic use*
- From:
Chinese Journal of Industrial Hygiene and Occupational Diseases
2022;40(4):255-259
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To explore the expulsion effect of sodium dimercaptopropanesulfonate (DMPS) on mercury in different organs of mercury poisoning and the therapeutic effect of glutathione (GSH) combined with antioxidant therapy on mercury poisoning. Methods: In February 2019, 50 SPF male SD rats were randomly divided into 5 groups, 10 rats in each group: A (saline negative control group) , B (HgCL2 positive control group) , treatment group (C: intramuscular injection of DMPS 15 mg/kg treatment, D: intramuscular injection of DMPS30 mg/kg treatment, E: intramuscular injection of DMPS 15 mg/kg and intraperitoneal injection of GSH200 mg/kg treatment) . Rats in group B, C, D and E were subcutaneously injected with mercury chloride solution (1 mg/kg) to establish a rat model of subacute mercury poisoning kidney injury. Rats in group A were subcutaneously injected with normal saline. After the establishment of the model, rats in the treatment group were injected with DMPS and GSH. Rats in group A and group B were injected with normal saline. At 21 d (treatment 7 d) and 28 d (treatment 14 d) after exposure, urine and blood samples of 5 rats in each group were collected. Blood biochemistry, urine mercury, urine microalbumin and mercury content in renal cortex, cerebral cortex and cerebellum were detected. Results: After exposure to mercury, the contents of mercury in renal cortex, cerebrum and cerebellum of rats in group B, C, D and E increased, and urine microalbumin increased. Pathology showed renal tubular injury and renal interstitial inflammation. Compared with group B, urinary mercury and renal cortex mercury in group C, D and E decreased rapidly after DMPS treatment, and there was no significant decrease in mercury levels in cerebellum and cerebral cortex of rats, accompanied by transient increase in urinary albumin after DMPS treatment (P<0.05) ; the renal interstitial inflammation in group E was improved after GSH treatment. There was a positive correlation between urinary mercury and the contents of mercury in renal cortex, cerebral cortex and cerebellum (r=0.61, 0.47, 0.48, P<0.05) . Conclusion: DMPS mercury expulsion treatment can significantly reduce the level of metal mercury in the kidney, and there is no significant change in the level of metal mercury in the cortex and cerebellum.
