Child ; Humans ; Paraquat ; poisoning ; Poisoning ; therapy

Aged ; Chlorpyrifos ; Dermatitis, Occupational ; etiology ; Female ; Humans ; Insecticides ; poisoning ; Middle Aged ; Organophosphate Poisoning ; complications

Acute Disease ; Adult ; Humans ; Male ; Occupational Diseases ; Phosgene ; poisoning

Objective　To observe the influence of dimet hylformamide(DMF) on 45　Ca transport in rat kidney mictochondria an d microsomes. Methods　Mitochondria and microsomes were is olated by ultracentrifugation.Radioactive isotope technique was used to examine the effects of DMF on 45　Ca uptake and release of mitochondria and microsomes and to explore the mechanism of renal injury. Results　(1)The 45　Ca uptake of mitochondria in DMF groups(130 μmol/L ,195 μmol/L) after 10 min incubation were (4.20±0.29)nmol/mg pro and (3.81± 0.42)nmol/mg pro respectively(P<0.05 or P<0.01),compared with control group (5.18±0.40)nmol/mg pro,and the 45　Ca uptake of microsomes in D MF groups(130 μmol/L,195 μmol/L) after 10 min incubation were (2.10±0.42) nmol/mg pro,(2.01±0.38)nmol/mg pro respectively(P<0.05 or P<0.01),compa red with control group (2.96±0.38)nmol/mg pro.The same results were gained afte r 20 min and 30 min incubation.(2)The 45　Ca remain in mitochondria of DMF groups(65 μmol/L,130 μmol/L,195 μmol/L) after 2 min incubation were (5.4 0±0.39)nmol/mg pro,(5.03±0.32)nmol/mg pro and (4.70±0.50)nmol/mg pro resp ectively(P<0.01),compared with control group［(6.01±0.40)nmol/mg pro］. The 45　Ca remain in microsomes of DMF groups(65 μmol/L,130 μmol/L,1 95 μmol/L) after 2 min incubation were (3.43±0.26)nmol/mg pro,(3.18±0.31) nmol/mg pro and (3.06±0.27)nmol/mg pro respectively(P<0.01),compare d with control group (4.06±0.32)nmol/mg pro,indicating increased release of calcium.The same results were gained 4 min and 8 min after incubation.There wer e dose-effect relationships between DMF and 45　Ca uptake or 45 　Ca release in both mitochondria and microsomes(r=0.918,0.895,0.886,0.8 46 respectively). Conclusion　DMF may induce disturbance of calcium homeost asis in rat kidney.

Objective　To observe the influence of dimet hylformamide(DMF) on 45　Ca transport in rat kidney mictochondria an d microsomes. Methods　Mitochondria and microsomes were is olated by ultracentrifugation.Radioactive isotope technique was used to examine the effects of DMF on 45　Ca uptake and release of mitochondria and microsomes and to explore the mechanism of renal injury. Results　(1)The 45　Ca uptake of mitochondria in DMF groups(130 μmol/L ,195 μmol/L) after 10 min incubation were (4.20±0.29)nmol/mg pro and (3.81± 0.42)nmol/mg pro respectively(P<0.05 or P<0.01),compared with control group (5.18±0.40)nmol/mg pro,and the 45　Ca uptake of microsomes in D MF groups(130 μmol/L,195 μmol/L) after 10 min incubation were (2.10±0.42) nmol/mg pro,(2.01±0.38)nmol/mg pro respectively(P<0.05 or P<0.01),compa red with control group (2.96±0.38)nmol/mg pro.The same results were gained afte r 20 min and 30 min incubation.(2)The 45　Ca remain in mitochondria of DMF groups(65 μmol/L,130 μmol/L,195 μmol/L) after 2 min incubation were (5.4 0±0.39)nmol/mg pro,(5.03±0.32)nmol/mg pro and (4.70±0.50)nmol/mg pro resp ectively(P<0.01),compared with control group［(6.01±0.40)nmol/mg pro］. The 45　Ca remain in microsomes of DMF groups(65 μmol/L,130 μmol/L,1 95 μmol/L) after 2 min incubation were (3.43±0.26)nmol/mg pro,(3.18±0.31) nmol/mg pro and (3.06±0.27)nmol/mg pro respectively(P<0.01),compare d with control group (4.06±0.32)nmol/mg pro,indicating increased release of calcium.The same results were gained 4 min and 8 min after incubation.There wer e dose-effect relationships between DMF and 45　Ca uptake or 45 　Ca release in both mitochondria and microsomes(r=0.918,0.895,0.886,0.8 46 respectively). Conclusion　DMF may induce disturbance of calcium homeost asis in rat kidney.

Objective: To study the therapy of cordyceps-astragalus-salvia miltiorrhiza in treating acute lung injury and pulmonary interstitial fibrosis induced by paraquat poisoning. Methods: All 120 adult Wister male rats were randomly assigned to three groups, the paraquat poisoning group (rats were intragastric administration paraquat 50 mg/kg body weight once at the beginning) , the cordyceps-astragalus-salvia miltiorrhiza therapy group (rats were given cordyceps-astragalus-salvia miltiorrhiza 90 mg/kg body weight intragastric administration half an hour after paraquat was given, then the same dose was given once a day) ; control group (rats were intragastric administration with physiological saline) . At 7th, 14th, 21st, and 28th day rats were sacrificed postanesthetic respectively after paraquat exposure, sample of lung tissue, bronchoalveolar lavage (BAL) , and venous blood were collected. GSH, SOD, TNF-α, TGF-β1, and HYP in plasma, bronchoalveolar lavage (BAL) , and the lung homogenates were determined. Optical microscope was performed to examine pathological changes in lung. Results: Each experimental time point paraquat group and the treatment group rats serum SOD content significantly lower than the control group (P<0.05) . Each experimental time point the treatment group rats serum SOD levels increased significantly than that of paraquat group (P<0.05) . Each experimental time point paraquat group rats serum GSH content significantly lower than that of the control group (P<0.05) . Treatment group rats 7 days time GSH content significantly lower than that of the control group (P<0.05) . Treatment group 21 days, 28 days GSH content was increased significantly than that of the paraquat group (P<0.05) . Each experimental time point paraquat group rats alveolar lavage SOD content was significantly lower than that of the control group (P<0.05) . Treatment group 7 days, 14 days time SOD content was significantly lower than that of the control group (P<0.05) , Treatment group 21 days, 28 days SOD content was increased significantly than that of the paraquat group (P<0.05) . Each experimental time point paraquat group and the treatment group rats alveolar lavage GSH content significantly were lower than that of the control group (P<0.05) . Treatment group days 14 and 21 days, 28 days GSH content was increased significantly than that of the paraquat group (P<0.05) . Each experimental time point paraquat group rats alveolar lavage TNF α levels was higher than that of the control group (P<0.05) . Treatment group 7 days, 14 days the rat alveolar lavage TNF α levels was higher than that of the control group (P<0.05) . Treatment group 21 days, 28 days TNF α content significantly was decreased than that of paraquat group (P<0.05) . Paraquat group days 14 and 21 days, 28 days HYP content was significantly higher than that of control group (P<0.05) . Treatment group 21 days HYP content was significantly higher than that of control group (P<0.05) . Treatment group 28 days time HYP content in lung tissue of rats was significantly decreased than that of the paraquat group (P<0.05) . Each experimental time point paraquat group rat lung tissue (tissue homogenate) TGF-β1 content was higher than that of the control group, the difference was statistically significant (P<0.05) . Under optical microscope, the tissue damage of lung was aggravated, and reduced after cordyceps-astragalus-salvia miltiorrhiza was administrated. Conclusion Cordyceps-astragalus-salvia miltiorrhiza can reduce inflammation factor releasing, and relieve lung injury. It has therapeutic effect on lung injury induced by paraquat poisoning.

Objective: To establish to paraquat poisoning acute lung injury animal model to study the therapeutic effect of Salvia polyphenols acid salt of paraquat-induced acute lung injury. Methods: Adult male Wister rats 120, were randomly divided into three groups: the paraquat exposure group, the start of the experiment to give a one-time 20% paraquat dope orally 50 mg/kg body weight of rats; salvianolate treatment group, the start of the experiment paraquat to give a one-time 20% the stock solution orally 50 mg/kg body weight of rats, and then given daily intraperitoneal injection of 200 mg/kg body weight of rats salvianolate; blank control group was given the same amount normal saline. The exposure group, the treatment group and control group rats were sacrificed after anesthesia in the 3rd, 7th, 14th, 21st day from the beginning of the experiment respectively, and taken out and preserved venous blood specimens and lung tissue to be tested. Venous detection heme oxygenase-1 (HO-1) , the lung tissue detection heme oxygenase-1 (HO-1) , hydroxyproline (HYP) . And do biopsy specimens from some of the lung tissue, HE and Masson staining observed by optical microscope. Results: Compared with control group, model group 7, 14, 21 days had elevated levels of serum and lung tissue HO-1 (all P<0.05) ; Treatment group 3, 7, 14, 21 days increased (all P<0.05) , and 3, 7, 14 days is higher than the model group (compared with model group, P<0.05) . Compared with control group, treatment group 3 days and model group, 14, 21 days HYP content in lung tissue increased significantly (all P<0.05) ; 21 days, compared with model group, HYP content of treatment group reduce obviously, the difference was statistically significant (P<0.05) . Optical microscope observation, lung tissue damage and aggravated with the experimental increase in the number of days, inflammatory cell infiltration, alveolar septal fibrosis gradually formed. The treatment group experimental animal lung tissue to reduce inflammation, lung fibrosis relief. Conclusion Paraquat (50 mg/kg body weight) to fill the stomach can be induced model of acute lung injury in the rats. The serum HO-1 expression and HO-1, HYP content in lung tissue increased obviously in model rats. Salvia miltiorrhiza polyphenols acid salt to a certain degree and stage influenced the expression of HO-1 and HYP, relieve acute lung injury and pulmonary fibrosis, has certain curative effect in the treatment of paraquat poisoning.

Objective: To report a case of rat poison with multiple hemorrhage after trauma. Methods: The clinical data of a case of rodenticide poisoning with hemorrhage as the first symptom admitted to a third-class a hospital in July 2018 were analyzed and summarized. Results: This patient is a rodent drug poisoning patient with hemorrhage as the first symptom.The disease was diagnosed as bromohamelin and bromadiolone poisoning through the analysis of poison detection because the rodent drug was taken in the market and the history of taking poison was concealed. The patient was given active comprehensive treatment of vitamin K1 and other drugs for clinical cure. Conclusion For patients with clinically unexplained hemorrhage, the possibility of rodenticide poisoning should be considered and the toxicant detection should be improved actively.

Objective: To explore the acute toxicity of Diquat in mice and to calculate the median lethal dose (LD₅₀) of Diquat to rats and observe the pathological changes of tissues and organs in rats with different concentrations of Diquat. Methods: Diquat solution of 50 mg/kg was prepared freshly with 1 000 mg of Diquat and dilute the solution with water to a total of 20 ml. A total of 99 healthy adult male Wistar rats were randomly divided into part one, part two and control groups. In the first part, 36 rats were randomly divided into 4 groups: 100 mg/kg group, 200 mg/kg group, 300 mg/kg group and 400 mg/kg group, which were treated with 100 mg/kg, 200 mg/kg, 300 mg/kg and 400 mg/kg of Diquat solution by gavage, respectively. The death and symptoms of poisoning after intragastric administration were recorded, and the maximum tolerated dose and absolute lethal dose were measured. In the second part, 54 rats were randomly divided into 6 groups: 200 mg/kg group, 220 mg/kg group, 240 mg/kg group, 260 mg/kg、280 mg/kg group and 300 mg/kg group, whichwere treated with 200 mg/kg, 220 mg/kg, 240 mg/kg, 260 mg/kg, 280 mg/kg and 300 mg/kg of Diquat solution by gavage, respectively. The survival of rats in different concentration of Diquat was observed and the LD₅₀ was calculated by Excel processing the formula of Koch's method. The control group were given equal volume water under the same experimental conditions. And moreover, the lungs, kidneys, hearts, livers, and brain tissues were collected and fixed by formaldehyde, embedded by paraffin, and sectioned for histopathological light microscopy. Results: The maximum tolerated dose was 240 mg/kg and the absolute lethal dose was 300 mg/kg. The LD₅₀ of Diquat for Rats was 280.58 mg/kg. The high-dose group had significantly more organ damage than the low-dose group after diquat poisoning. Conclusion The determination of the half-lethal dose of diquat, at the same time observed multiple organs damaged in rats after the diquat quickly poisoned. Kidneys, lungs and heart might be the main organ which was heavily damaged. With the extension of observation time, the organ damage of rats exposed to small doses gradually stabilized.

Objective: To investigate a poisonous mushroom poisoning incident and analyze its clinical data. Methods: Investigate a poisonous mushroom poisoning incident in a place in Shandong in July 2018, at the same time, the clinical data of 2 cases of mushroom poisoning were analyzed and summarized. Results: The incident was caused by a poisoning incident caused by residents eating poisonous mushrooms. The poisonous mushroom in this incident was identified as a scaled white goose cream. Two patients with poisoning developed gastrointestinal symptoms such as nausea and vomiting, abdominal pain and diarrhea, and liver damage occurred later. After active rescue and treatment, one patient was discharged from hospital, and the other patient developed acute pulmonary embolism during the treatment. He was discharged after interventional thrombolysis and follow-up treatment. Conclusion After investigation, the incident was caused by the ingestion of poisonous mushrooms mainly based on the scalloped white goose cream. After active treatment, they were cured and discharged.