2.The toxicological mechanisms and detoxification of depleted uranium exposure.
Yong-Chao YUE ; Ming-Hua LI ; Hai-Bo WANG ; Bang-Le ZHANG ; Wei HE
Environmental Health and Preventive Medicine 2018;23(1):18-18
Depleted uranium (DU) has been widely applied in industrial and military activities, and is often obtained from producing fuel for nuclear reactors. DU may be released into the environment, polluting air, soil, and water, and is considered to exert both radiological and chemical toxicity. In humans and animals, DU can induce multiple health effects, such as renal tubular necrosis and bone malignancies. This review summarizes the known information on DU's routes of entry, mechanisms of toxicity, and health effects. In addition, we survey the chelating agents used in ameliorating DU toxicity.
Animals
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Chelating Agents
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pharmacology
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Humans
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Inactivation, Metabolic
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Radiation-Protective Agents
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pharmacology
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Uranium
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metabolism
;
toxicity
3.Effect of exogenous Ca2+ on protective infection of Pinellia ternata and accumulation of major components under high temperature stress.
Can-wen LI ; Kang-cai WANG ; Qing-yun LUO ; Xing-li TANG
China Journal of Chinese Materia Medica 2012;37(19):2875-2878
OBJECTIVETo study the effect of exogenous Ca2+ on protective infection of Pinellia ternata and accumulation of major components under high temperature stress.
METHODThe soilless cultivation experiment was applied, stress resistance index of P. ternata leaves, statistics the rate of lodge P. ternata,the content of oxalate in different places in the plant, the content of total alkaloids, total organic acids and glucosine in P. ternata tubers were measured based on different concentrations of exogenous Ca2+.
RESULTThe test results showed that, at lower concentrations of Ca2+ treatments, the rate of lodge P. ternata was higher than that of the others. With Ca2+ concentration increasing, activities of SOD and POD initially increased and then decreased, however, proline level tended to be down then up. Soluble oxalic acid content was lower than the content of unhandled treatment in P. ternata leaves and tubers; with Ca2+ concentration increasing, soluble oxalic acidl content and yield showed a tendency of decrease after increase in the leaves and tubers. Compared with other treatments, spraying 400 mg x L(-1) Ca2+ significantly enhanced the accumulation of total alkaloid and guanosine in P. ternata tubers. At Lower concentrations of Ca2+, the content of total free organic acid was higher in the tuber.
CONCLUSIONWith the treatment of Ca2+ the capacity of heat resistance was improved in P. ternata plants, the rate of lodge P. ternata was postponed, growing period was extended and corresponding production has increased by spraying exogenous Ca2+.
Calcium Compounds ; pharmacology ; Hot Temperature ; Pinellia ; chemistry ; drug effects ; Protective Agents ; pharmacology ; Stress, Physiological
4.Delonix regia: historic perspectives and modern phytochemical and pharmacological researches.
Anuj MODI ; Vijay MISHRA ; Ajita BHATT ; Aviral JAIN ; Mohd Hashim MANSOORI ; Ekta GURNANY ; Vimal KUMAR
Chinese Journal of Natural Medicines (English Ed.) 2016;14(1):31-39
Delonix regia (Bojer ex Hook) Raffin (Fabaceae), also known as flame of forest, is a semi-deciduous tree, distributed throughout Madagascar, India, Africa, and Northern Australia. Various parts of the plant are traditionally used for the treatment of different ailments such as inflammation, rheumatism, bronchitis, diabetes, anemia, fever, gynecological disorders, and pneumonia. The plant possess antioxidant, hepatoprotective, gastroprotective, wound healing, antiarthritic, larvicidal, antimalarial, antiemetic, antibacterial, antifungal, antiinflammatory, analgesic, antidiarrhoeal, antiheamolytic, diuretic, and anthelmintic activities. This review is an up-to-date compilation on its traditional uses in context to phytochemical and pharmacological perspectives.
Animals
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Anti-Inflammatory Agents
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pharmacology
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Antiemetics
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pharmacology
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Antioxidants
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pharmacology
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Fabaceae
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chemistry
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Humans
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Hypoglycemic Agents
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pharmacology
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Plant Extracts
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pharmacology
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Protective Agents
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pharmacology
5.Pharmacology of mangostins and their derivatives: A comprehensive review.
Ming-Hui WANG ; Kuo-Jun ZHANG ; Qin-Lan GU ; Xiao-Ling BI ; Jin-Xin WANG
Chinese Journal of Natural Medicines (English Ed.) 2017;15(2):81-93
Mangosteen (Garcinia mangostana Linn.) is a well-known tropical tree indigenous to Southeast Asia. Its fruit's pericarp abounds with a class of isoprenylated xanthones which are referred as mangostins. Numerous in vitro and in vivo studies have shown that mangostins and their derivatives possess diverse pharmacological activities, such as antibacterial, antifungal, antimalarial, anticarcinogenic, antiatherogenic activities as well as neuroprotective properties in Alzheimer's disease (AD). This review article provides a comprehensive review of the pharmacological activities of mangostins and their derivatives to reveal their promising utilities in the treatment of certain important diseases, mainly focusing on the discussions of the underlying molecular targets/pathways, modes of action, and relevant structure-activity relationships (SARs). Meanwhile, the pharmacokinetics (PK) profile and recent toxicological studies of mangostins are also described for further druggability exploration in the future.
Animals
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Anti-Infective Agents
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pharmacology
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Anticarcinogenic Agents
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pharmacology
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Antineoplastic Agents, Phytogenic
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pharmacology
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Antioxidants
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pharmacology
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Cardiovascular Agents
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pharmacology
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Fruit
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chemistry
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Garcinia mangostana
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chemistry
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Humans
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Neuroprotective Agents
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pharmacology
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Phytotherapy
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Plant Extracts
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pharmacology
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Protective Agents
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pharmacology
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Xanthones
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pharmacology
6.Renoprotective effects of matrine on experimental glomerulosclerosis in rats.
Chinese Journal of Pediatrics 2004;42(10):737-740
OBJECTIVEMatrine has an anti-fibrosis effect, such as hepatic cirrhosis and derma fibrosis, while its effect on glomerulosclerosis is unknown. The purpose of this study was to analyze the renoprotective effects of matrine on experimental glomerulosclerosis in rats and inquire into its mechanisms.
METHODSThe rats were randomly assigned to following groups: normal control group, model control group, benazepril treatment group, matrine 100 mg/kg treatment group and matrine 50 mg/kg treatment group. The rats of normal control group were subjected to sham operation and were injected with normal saline via the tail vein one week later. The rats of the other groups were uninephrectomized and injected with adriamycin (5 mg/kg) via the tail vein one week later. The dose of benazepril was 6 mg/kg. Both matrine and benazepril were given by gastric perfusion from the first day after the operation. The level of urinary protein was measured at the 2nd, 4th and 6th week after the operation. The serum total protein and albumin, serum creatinine, blood urea nitrogen (BUN) were tested only at the 6th week after operation. Renal pathology changes were evaluated at the 6th week as well. Immunohistochemistry was used to detect the expression of fibronectin (FN), laminin (LN), connective tissue growth factor (CTGF) and transforming growth factor-beta1 (TGF-beta1) in glomeruli.
RESULTSMatrine and benazepril not only reduced the excretion of urinary protein and the level of serum creatinine and BUN, but also significantly ameliorated glomerular mesangial proliferation and glomerular sclerosis (P < 0.05, respectively). Immunohistochemical staining indicated that there was an increasing FN, LN, CTGF and TGF-beta1 expression in model control group as compared to the three treatment groups (P < 0.05). Matrine 100 mg/kg treatment group and benazepril treatment group showed much more advantages than matrine 50 mg/kg treatment group (P < 0.05), but there was no significant difference between the former two groups (P > 0.05).
CONCLUSIONMatrine has a renoprotective effect on experimental glomerulosclerosis in rats, the possible mechanism might relate to the reduction of the TGF-beta1 negative function via CTGF, which will inhibit the activation and proliferation of glomerular intrinsic cells, decrease the secretion of ECM accordingly.
Alkaloids ; pharmacology ; Animals ; Benzazepines ; pharmacology ; Kidney ; drug effects ; Kidney Diseases ; prevention & control ; Kidney Glomerulus ; drug effects ; Protective Agents ; pharmacology ; Quinolizines ; pharmacology ; Rats ; Renal Agents ; pharmacology
7.Phytochemical analysis of medicinal plants with kidney protective activities.
Eric Jung-Chi LIEN ; Linda Lin-Min LIEN ; Rubin WANG ; Jeffrey WANG
Chinese journal of integrative medicine 2012;18(10):790-800
In view of the increasing number of patients undergoing kidney dialysis or transplant every year, a survey of the literature on renal protective medicinal plants was undertaken. Most of them are from traditional Chinese medicine (TCM). Although many of the medicinal herbs reported have not been investigated in terms of active chemical ingredients, some do have compounds well characterized. They fall into a wide range of structures. Several groups of compounds with well established activities are discussed. These include: antioxidant phenolic compounds like tannins, flavonoids, isoflavonoids, unsaturated organic acids and lignans; circulation enhancing compounds like saponins, and basic alkaloids with multiple targets (G-protein coupled receptors). Also presented are proinflammatory and antiinflammatory fatty acids like linoleic (n-6) and α-linolenic (n-3) acids, respectively. Attention is also drawn to the plants containing nephrotoxic aristolochic acid. Different directions of future research are also presented. We hope that this review may provide some leads for new drug discovery and development, and more rational application of TCM.
Animals
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Humans
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Kidney
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drug effects
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Plants, Medicinal
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chemistry
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Protective Agents
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chemistry
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pharmacology
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Structure-Activity Relationship
8.Studies on external auditory canal injury in rabbits under simulated 50 mnitrogen-oxygen saturation diving and protective effect of compound aluminium acetate solution.
Ming-ke WANG ; Jian-bo BA ; Wen-bin WU ; Xiong-li XU ; Jia HE
Chinese Journal of Applied Physiology 2016;32(1):58-64
Acetates
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pharmacology
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Animals
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Disease Models, Animal
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Diving
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adverse effects
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Ear Canal
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injuries
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Nitrogen
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Oxygen
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Protective Agents
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pharmacology
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Rabbits
9.Effect of verapamil and nitroglycerin on transplanted lung function in canines.
Zhibin JIANG ; Ping HU ; Jianxin LIU ; Dianjun WANG ; Longyu JIN ; Chao HONG
Journal of Central South University(Medical Sciences) 2014;39(8):802-806
OBJECTIVE:
To investigate the protective effect of combined administration of verapamil and nitroglycerin on the function of canine transplanted lungs.
METHODS:
Twenty orthotopic left lung transplantations were performed in 40 canines, which were randomly divided into 4 groups. In group I (control), the donor lungs were perfused and preserved with LPD solution, while group II with LPD solution plus verapamil 0.1 g/L, group III with LPD solution plus nitroglycerin 0.1g/L, and group IV with LPD solution plus verapamil 0.1 g/L and nitroglycerin 0.1 g/L. Hemodynamics and graft gas exchange were assessed 0, 2 and 4 h after the operation. The lung grafts were harvested to measure the wet/dry weight ratio, malondialdehyde (MDA) contents and superoxide dismutase (SOD) activity.
RESULTS:
Compared with group I, II and III, the mean pulmonary artery pressure (MPAP), pulmonary vascular resistance index (PVRI), partial pressure of oxygen in arterial blood (PaO₂), dynamic compliance (Cdyn) and alveolar-arterial oxygen tension volume [P(A- a)O₂] in group IV were improved significantly (P<0.05). No significant difference in the partial pressure of carbondioxide (PaCO₂) and peak inspiratory pressure (PIP) was observed in the 4 groups (P>0.05). In group IV, the wet/dry weight ratio and MDA contents were lower than those in the other 3 groups, and the SOD activity was significantly higher than that of the other 3 groups (P<0.05).
CONCLUSION
Verapamil and nitroglycerin in LPD solution can protect the respiratory function of canine lung grafts by attenuating pulmonary edema and oxidative stress.
Animals
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Blood Gas Analysis
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Dogs
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Hemodynamics
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Lung
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Lung Transplantation
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Nitroglycerin
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pharmacology
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Organ Preservation
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Protective Agents
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Reperfusion Injury
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Verapamil
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pharmacology
10.Protective effect and mechanism of curcumin on aorta in rats with metabolic syndrome.
Li-Jie YAN ; Shun-Bao WANG ; Xian-Qing WANG ; Xue-Ming CAO
China Journal of Chinese Materia Medica 2019;44(21):4685-4690
To investigate the protective effect and mechanism of curcumin on aorta in rats with metabolic syndrome,72 SD rats were randomly divided into blank control group,model control group,positive control group,curcumin low,middle and high dose groups.The rat model of metabolic syndrome was established in all groups except the blank control group. After the intervention by curcumin,the blood pressure,blood lipid,blood glucose,serum insulin and insulin sensitivity index were measured. The contents of serum leptin(LP),adiponectin(ADP) and tumor necrosis factor-α(TNF-α) in rat aorta were detected by enzyme-linked immunosorbent assay(ELISA),and the pathological changes of rat thoracic aorta were observed by HE staining and electron microscope scanning. Western blot assay was used to detect the expression of inducible nitric oxide synthase(i NOS) and endothelial nitric oxide synthase(e NOS) in rats. The results showed that the blood lipid level,fasting blood glucose,fasting insulin,insulin sensitivity index,systolic blood pressure,LP,TNF-α and intima/media thickness ratio in the model control group were significantly higher than those in the blank control group. As compared with the model control group,the levels of blood lipids,fasting blood glucose,fasting insulin,insulin sensitivity index,systolic blood pressure,LP,TNF-α and intima/media thickness ratio were significantly decreased in positive control group,low,middle and high dose curcumin groups. The difference was statistically significant. The results of HE staining showed that the intima of the thoracic aorta in the model group was significantly thickened; the endothelial cell membrane was wrinkled and the organelle was ruptured. The intima of the thoracic aorta in the positive control group was slightly thickened and the structure of endothelial cells was intact,with no foam cells and no abnormality in the adventitia. There was no significant thickening of the thoracic aorta in the low,middle and high dose curcumin groups,and the endothelial cells were still intact. The results of Western blot assay showed that the expression levels of i NOS and e NOS were decreased significantly in the model group,while the expression levels of i NOS and e NOS were increased significantly in the positive control group and curcumin groups. The results indicated that curcumin had a certain protective effect on the aorta of rats with metabolic syndrome and improves the aortic endothelial dysfunction,and its mechanism may be related to the fact that curcumin could reduce the production of oxygen free radicals and up-regulate the expression of i NOS and e NOS in aorta.
Animals
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Aorta
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Aorta, Thoracic
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Curcumin/pharmacology*
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Endothelial Cells
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Metabolic Syndrome
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Protective Agents/pharmacology*
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Rats
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Rats, Sprague-Dawley