1.A case of delirium caused by carbamate insecticide poisoning treated with penehyclidine hydrochloride.
Yi Mu ZHENG ; Yun Xia XIA ; Zan Mei ZHAO ; Xiao LI
Chinese Journal of Industrial Hygiene and Occupational Diseases 2022;40(10):785-786
		                        		
		                        			
		                        			The incidence of carbamate insecticide poisoning has increased gradually in recent years, and anticholinergic drugs are the specific antidotes. In 2020, the Peking University Third Hospital admitted a patient with carbamate insecticide poisoning, whose main clinical manifestations were dizziness, vomiting and blurred vision. During the treatment with penehyclidine hydrochloride, the patient developed delirium. This paper retrospectively analyzed the clinical data and treatment process of the patient to improve people's understanding of the side effects of penhyclidine hydrochloride in the treatment of insecticide poisoning.
		                        		
		                        		
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Insecticides
		                        			;
		                        		
		                        			Retrospective Studies
		                        			;
		                        		
		                        			Hydrochloric Acid
		                        			;
		                        		
		                        			Carbamates/therapeutic use*
		                        			;
		                        		
		                        			Delirium
		                        			;
		                        		
		                        			Poisoning/therapy*
		                        			;
		                        		
		                        			Organophosphate Poisoning/drug therapy*
		                        			
		                        		
		                        	
2.Study on the difference of curative effect of conventional mercury displacement treatment on mercury in brain and kidney.
Zhen Zhen GAO ; Yu Jie PAN ; Jing MA ; Hui Ling LI ; Xue MEI ; Yu Guo SONG
Chinese Journal of Industrial Hygiene and Occupational Diseases 2022;40(4):255-259
		                        		
		                        			
		                        			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.
		                        		
		                        		
		                        		
		                        			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*
		                        			
		                        		
		                        	
3.The influence of sodium bicarbonate combined with ulinastatin on cholinesterase activity for patients with acute phoxim pesticide poisoning.
Bo ZHAO ; Lanju YANG ; Lei XIAO ; Baoquan SUN ; Xianbao ZOU ; Dongmei GAO ; Xiandong JIAN
Chinese Journal of Industrial Hygiene and Occupational Diseases 2016;34(1):53-55
OBJECTIVETo observe the effect of sodium bicarbonate combined with ulinastatin on cholinesterase activity for patients with acute phoxim pesticide poisoning.
METHODSA total of 67 eligible patients with acute phoxim pesticide poisoning, Who were admitted to the emeryency department of hospital from March 2011 to February 2014, Acording to different treatments au patients were randomly divided into the conventional treatment group (n=34) and the sodium bicarbonate+ulinastatin group (n=35) . The conventional treatment group were given thorough gastric lavage with water, the sodium bicarbonate + ulinastatin group were given gastric lavage with 2% sodium bicarbonate solution. Both groups were given such treatments as catharsis, administration of oxygen, fluid infusion, diuresis, and antidotes such as atropine and pralidoxime methylchloride. On the basis of comprehensive treatment, people in the sodium bicarbonate+ulinastatin group were given 5% sodium bicarbonate injection and ulinastatin. The clinical effect of the two groups were compared.
RESULTSThe serum cholinesterase activity of the sodium bicarbonate+ulinastatin group was significantly higher than the conventional treatment group from the 5th day, and the difference was statistically significant (P<0.05) . The total atropine dosage, total pralidoxime methylchloride dosage and hospitalization days were better than the conventional treatment group, and the differences were statistically significant (P<0.05) . The difference in the time of atropinization between the two groups was not statistically significant (P>0.05) . The results of arterial blood pH, HCO3- of the sodium bicarbonate + ulinastatin group were higher than the conventional treatment group, and the difference of HCO3- at the 10th day was statistically significant (P<0.05) .
CONCLUSIONSSodium bicarbonate combined with ulinastatin can improve the therapeutic effect and reduce complications in the treatment of acute phoxim pesticide poisoning, and have beneficial effects on the recovery of cholinesterase activity.
Atropine ; therapeutic use ; Cholinesterases ; metabolism ; Glycoproteins ; therapeutic use ; Humans ; Organophosphate Poisoning ; drug therapy ; Organothiophosphorus Compounds ; poisoning ; Pesticides ; poisoning ; Pralidoxime Compounds ; therapeutic use ; Sodium Bicarbonate ; therapeutic use
4.Antioxidant activities of crude phlorotannins from Sargassum hemiphyllum.
Zhi-Li ZHAO ; Xiao-Qing YANG ; Zhong-Qing GONG ; Ming-Zhu PAN ; Ya-Li HAN ; Yi LIU
Journal of Huazhong University of Science and Technology (Medical Sciences) 2016;36(3):449-455
		                        		
		                        			
		                        			Brown algae are well known as a source of biologically active compounds, especially those having antioxidant activities, such as phlorotannins. In this study we examined the antioxidant activities of crude phlorotannins extracts (CPEs) obtained from Sargassum hemiphyllum (SH) and fractionated according to the molecular weights. When CPEs were administrated at a dose of 30 mg/kg to Kunming mice pre-treated with carbon tetrachloride (CCl4), the levels of oxidative stress indicators in the liver, kidney and brain were significantly reduced in vivo. All the components of various molecular weight fractions of CPEs exhibited greater scavenging capacities in clearing hydroxyl free radical and superoxide anion than the positive controls gallic acid, vitamin C and vitamin E. Particularly, the components greater than 30 kD obtained from ethyl acetate phase showed the highest antioxidant capacities. These results indicated that SH is a potential source for extracting phlorotannins, the algal antioxidant compounds.
		                        		
		                        		
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Antioxidants
		                        			;
		                        		
		                        			isolation & purification
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			Ascorbic Acid
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			Brain
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			Carbon Tetrachloride
		                        			;
		                        		
		                        			antagonists & inhibitors
		                        			;
		                        		
		                        			toxicity
		                        			;
		                        		
		                        			Carbon Tetrachloride Poisoning
		                        			;
		                        		
		                        			drug therapy
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			Chemical Fractionation
		                        			;
		                        		
		                        			methods
		                        			;
		                        		
		                        			Gallic Acid
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			Hydroxyl Radical
		                        			;
		                        		
		                        			antagonists & inhibitors
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Kidney
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			Liquid-Liquid Extraction
		                        			;
		                        		
		                        			methods
		                        			;
		                        		
		                        			Liver
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Mice
		                        			;
		                        		
		                        			Mice, Inbred Strains
		                        			;
		                        		
		                        			Oxidation-Reduction
		                        			;
		                        		
		                        			Oxidative Stress
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			Phaeophyta
		                        			;
		                        		
		                        			chemistry
		                        			;
		                        		
		                        			Sargassum
		                        			;
		                        		
		                        			chemistry
		                        			;
		                        		
		                        			Superoxides
		                        			;
		                        		
		                        			antagonists & inhibitors
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Tannins
		                        			;
		                        		
		                        			isolation & purification
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			Vitamin E
		                        			;
		                        		
		                        			pharmacology
		                        			
		                        		
		                        	
5.Effect of total flavonoids from astragalus complanatus on paraquat poisoning-induced pulmonary fibrosis in rats and its mechanisms.
Zhijian ZHANG ; Yaoyao DONG ; Yunfan HUANG ; Libo PENG ; E-mail: PLBBNICU@YEAH.NET.
Chinese Journal of Industrial Hygiene and Occupational Diseases 2015;33(11):838-840
OBJECTIVETo investigate the effects of total flavonoids from astragalus complanatus (FAC) on paraquat poisoning-induced pulmonary fibrosis in rats.
METHODSThe rats were divided into six groups randomly: control group, paraquat group, prednisolone group and FAC low-dose, middle-dose, high-dose group. Pulmonary fibrosis model was replicated by intratracheal injection of paraquat. In the mext day,the rats were treated by intragastric administration once a day. After 28 days, the rats were sacrificed. The lung index and the levels of HYP and T-AOC were measured, and the pathologic changes of the lung tissue were obtained by HE staining. The levels of TGF-β, Smad2, α-SMA protein were analyzed by Western blot.
RESULTSFAC improved the activity of T-AOC in serum and reduced pulmonary index and the content of HYP as well (P<0.05 or P<0.01), the alveolitis and fibrosis extent were attenuated. The expression of Smad2 significantly decreased in groups of FAC low-dose, middle-dose and high-dose (0.31±0.11, 0.45±0.12 and 0.30±0.05) as compared with that of the PQ group (0.85±0.34) (P<0.05). The expression of α-SMA significantly decreased in groups of FAC low-dose, middle-dose and high-dose (0.31±0.11, 0.35±0.07 and 0.32±0.10) as compared with that of the PQ group (0.45±0.08) (P<0.05). The expression of TGF-β significantly decreased in groups of FAC low-dose, middle-dose and high-dose (0.35±0.04, 0.27±0.05 and 0.18±0.04)as compared with that of the PQ group (0.63±0.11) (P<0.05).
CONCLUSIONFAC can alleviate PQ-induced pulmonary fibrosis in rats through inhibiting TGF-β/Smad signaling pathway.
Actins ; metabolism ; Animals ; Astragalus Plant ; chemistry ; Flavonoids ; pharmacology ; Lung ; pathology ; Paraquat ; poisoning ; Phytochemicals ; pharmacology ; Pulmonary Fibrosis ; chemically induced ; drug therapy ; Rats ; Smad2 Protein ; metabolism ; Transforming Growth Factor beta ; metabolism
7.Effects of polygala on the neurogenesis of manganese poisoned mice.
Xuechao JING ; Li QIN ; Boning YANG
Chinese Journal of Industrial Hygiene and Occupational Diseases 2015;33(3):207-210
OBJECTIVETo investigate the effects of polygala on leaning and memory and the expression of Microtubule associated protein on manganese poisoned mice.
METHODS60 female Kunming mice were randomly and equally divided into 5 group. They are normal control group (CG), manganese poisoned group (MG), manganese poisoned with polygala high dose group (MHG), manganese poisoned with polygala middle dose group (MMG), manganese poisoned with polygala low dose group (MLG). The model of manganese poisoned mice was prepared of the way of intraperitoneal injection of manganese chloride (MnCl2 15 mg/kg), the spatial learning and memory ability was tested by Morris water maze, the Doublecortin (DCX) was tested by the way of immunofluorescent staining in the SVZ and SGZ.
RESULTIn the navigation test, compared with MG, the escape latency of MHG, MMG and MLG were significantly decreased (P < 0.05), in space exploration experiments, MHG, MMG, MLG compared with MG, the number increased significantly across platforms (P < 0.05). compared with MG, the DCX expression of MHG, MMG and MLG were significantly increased (P < 0.05).
CONCLUTIONThe leaning and memory ability of manganese poisoned mice can be improved by the polygala, and the mechanism may be related to promote the expression of DCX and neurogenesis in the brain.
Animals ; Female ; Manganese Poisoning ; drug therapy ; Maze Learning ; drug effects ; Memory ; drug effects ; Mice ; Microtubule-Associated Proteins ; drug effects ; Neurogenesis ; drug effects ; Neuropeptides ; drug effects ; Plant Extracts ; pharmacology ; Polygala ; chemistry
8.Research Progress on Forensic Toxicology of Z-drugs.
Yong-zhi ZHANG ; Hong-yuan HE ; Cai-meng SHE ; Jie LIAN
Journal of Forensic Medicine 2015;31(4):293-297
		                        		
		                        			
		                        			The Z-drugs (zolpidem, zopiclone, and zaleplon), as the innovative hypnotics, have an improvement over the traditional benzodiazepines in the management of insomnia. Z-drugs have significant hypnotic effects by reducing sleep latency and improving sleep quality, though duration of sleep may not be significantly increased. As benzodiazepines, Z-drugs exert their effects through increasing the transmission of γ-aminobutyric acid. Z-drugs overdose are less likely to be fatal, more likely would result in poisoning. Z-drugs can be detected in blood, urine, saliva, and other postmortem specimens through liquid chromatography-mass spectrometry techniques. Zolpidem and zaleplon exhibit significant postmortem redistribution. Z-drugs have improved pharmacokinetic profiles, but incidence of neuropsychiatric sequelae, poisoning, and death may prove to be similar to the other hypnotics. This review focuses on the pharmacology and toxicology of Z-drugs with respect to their adverse effect profile and toxicity and toxicology data in the field of forensic medicine.
		                        		
		                        		
		                        		
		                        			Acetamides/poisoning*
		                        			;
		                        		
		                        			Azabicyclo Compounds/poisoning*
		                        			;
		                        		
		                        			Drug Overdose
		                        			;
		                        		
		                        			Forensic Medicine/trends*
		                        			;
		                        		
		                        			Forensic Toxicology/trends*
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Hypnotics and Sedatives/poisoning*
		                        			;
		                        		
		                        			Piperazines/poisoning*
		                        			;
		                        		
		                        			Pyridines/poisoning*
		                        			;
		                        		
		                        			Pyrimidines/poisoning*
		                        			;
		                        		
		                        			Sleep Initiation and Maintenance Disorders/drug therapy*
		                        			;
		                        		
		                        			Zolpidem
		                        			
		                        		
		                        	
9.Preventive effects of the polysaccharide of Larimichthys crocea swim bladder on carbon tetrachloride (CCl4)-induced hepatic damage.
Xin ZHAO ; Yu QIAN ; Gui-Jie LI ; Jun TAN
Chinese Journal of Natural Medicines (English Ed.) 2015;13(7):521-528
		                        		
		                        			
		                        			The aim of the present study was to determine the preventive effects of the polysaccharide of Larimichthys crocea swim bladder (PLCSB) on CCl4-induced hepatic damage in ICR mice. The in vitro preventive effects of PLCSB on CCl4-induced liver cytotoxic effect were evaluated in BRL 3A rat liver cells using the MTT assay. The serum levels of AST, ALT, and LDH in mice were determined using commercially available kits. The levels of IL-6, IL-12, TNF-α, and IFN-γ were determined using ELISA kits. The pathological analysis of hepatic tissues was performed with H and E staining, and the gene and protein expressions were determined by RT-PCR and Western blotting, respectively. PLCSB (20 μg·mL(-1)) could increase the growth of BRL 3A rat liver cells treated with CCl4. The serum levels of AST, ALT, and LDH were significantly decreased when the mice were treated with two doses of PLCSB, compared with the control mice (P < 0.05). PLCSB-treated groups also showed reduced levels of the serum pro-inflammatory cytokines IL-6, IL-12, TNF-α, and IFN-γ. PLCSB could decrease the liver weight, compared to the CCl4-treated control mice. The histopathology sections of liver tissues in the 100 mg·kg(-1) PLCSB group indicated that the animals were recovered well from CCl4 damage, but the 50 mg·kg(-1) PLCSB group showed necrosis to a more serious extent. The 100 mg·kg(-1) PLCSB group showed significantly decreased mRNA and protein expression levels of NF-κB, iNOS, and COX-2, and increased expression of IκB-α compared with the CCl4-treated control group. In conclusion, PLCSB prevented from CCl4-induced hepatic damage in vivo.
		                        		
		                        		
		                        		
		                        			Animal Structures
		                        			;
		                        		
		                        			chemistry
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Biological Products
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			therapeutic use
		                        			;
		                        		
		                        			Carbon Tetrachloride
		                        			;
		                        		
		                        			Carbon Tetrachloride Poisoning
		                        			;
		                        		
		                        			drug therapy
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			Chemical and Drug Induced Liver Injury
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			prevention & control
		                        			;
		                        		
		                        			Cyclooxygenase 2
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Cytokines
		                        			;
		                        		
		                        			blood
		                        			;
		                        		
		                        			I-kappa B Proteins
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Inflammation Mediators
		                        			;
		                        		
		                        			blood
		                        			;
		                        		
		                        			Liver
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Mice, Inbred ICR
		                        			;
		                        		
		                        			NF-KappaB Inhibitor alpha
		                        			;
		                        		
		                        			NF-kappa B
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Necrosis
		                        			;
		                        		
		                        			Nitric Oxide Synthase Type II
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Perciformes
		                        			;
		                        		
		                        			Polysaccharides
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			therapeutic use
		                        			;
		                        		
		                        			RNA, Messenger
		                        			;
		                        		
		                        			metabolism
		                        			
		                        		
		                        	
10.Kind and Estimated Stocking Amount of Antidotes for Initial Treatment for Acute Poisoning at Emergency Medical Centers in Korea.
Chang Hwan SOHN ; Seung Mok RYOO ; Kyoung Soo LIM ; Won KIM ; Hoon LIM ; Bum Jin OH
Journal of Korean Medical Science 2014;29(11):1562-1571
		                        		
		                        			
		                        			Antidotes for toxicological emergencies can be life-saving. However, there is no nationwide estimation of the antidotes stocking amount in Korea. This study tried to estimate the quantities of stocking antidotes at emergency department (ED). An expert panel of clinical toxicologists made a list of 18 emergency antidotes. The quantity was estimated by comparing the antidote utilization frequency in a multicenter epidemiological study and the nation-wide EDs' data of National Emergency Department Information System (NEDIS). In an epidemiological study of 11 nationwide EDs from January 2009 to December 2010, only 92 (1.9%) patients had been administered emergency antidotes except activated charcoal among 4,870 cases of acute adult poisoning patients. Comparing with NEDIS data, about 1,400,000 patients visited the 124 EDs nationwide due to acute poisoning and about 103,348 adult doses of the 18 emergency antidotes may be required considering poisoning severity score. Of these, 13,224 (1.9%) adult doses of emergency antidotes (575 of atropine, 144 of calcium gluconate or other calcium salts, 2,587 of flumazenil, 3,450 of N-acetylcysteine, 5,893 of pralidoxime, 287 of hydroxocobalamin, 144 of sodium nitrite, and 144 of sodium thiosulfate) would be needed for maintaining the present level of initial treatment with emergency antidotes at EDs in Korea.
		                        		
		                        		
		                        		
		                        			Acute Disease
		                        			;
		                        		
		                        			Antidotes/*supply & distribution/therapeutic use
		                        			;
		                        		
		                        			Databases, Factual
		                        			;
		                        		
		                        			Emergency Service, Hospital
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Poisoning/*drug therapy
		                        			;
		                        		
		                        			Republic of Korea
		                        			
		                        		
		                        	
            
Result Analysis
Print
Save
E-mail