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1.
Huan Jing Ke Xue ; 43(6): 3058-3065, 2022 Jun 08.
Artigo em Chinês | MEDLINE | ID: mdl-35686775

RESUMO

To reveal the characteristics of organic phosphorus release from lake sediments and its potential impact on water quality, six lake sediments from Yunnan Plateau and the middle and lower reaches of the Yangtze River in China were selected. We studied the differences in the kinetics of dissolved organic phosphorus (DOP) and dissolved inorganic phosphorus (SRP) release from sediments. The effects of organic phosphorus morphology and dissolved organic matter (DOM) characteristics on sediment phosphorus release were investigated, and the water quality risks of sediment DOP release were discussed. The results showed that:① the release kinetics of sediment DOP and SRP were similar; both followed the second-order kinetic model, starting with a rapid release phase, followed by a slow release, and the release curve gradually leveled off and reached the maximum release. ② The release of organic phosphorus was related to organophosphorus morphology and organic matter. Active organic phosphorus (LOP) and medium active organic phosphorus (MLOP) were the DOP forms mainly released into the overlying water during the rapid release phase. The proportion of LOP and MLOP to total organic phosphorus (DTP) decreased in the late release stage, whereas the proportion of non-active organic phosphorus (NLOP) increased; further, the degree of humification and aromaticity of organic matter gradually increased with phosphorus release, and its activity decreased, resulting in a slower release rate at the later stage. ③ Compared with that of SRP, the risk of DOP release was higher, accounting for 47%-77% of the total amount of DTP. It was also found that the higher the nutrient level of the lake, the greater the release of DOP and the higher the water quality risk. Therefore, not only the release of inorganic phosphorus but also that of organic phosphorus should be of concern in the process of phosphorus release from lake sediments to prevent the underestimation of phosphorus release and water quality risk.


Assuntos
Fósforo , Poluentes Químicos da Água , China , Sedimentos Geológicos , Cinética , Lagos , Fósforo/análise , Poluentes Químicos da Água/análise , Qualidade da Água
2.
J Asian Nat Prod Res ; 24(11): 1008-1017, 2022 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-34969326

RESUMO

Two new polycyclic polyprenylated acylphloroglucinols (PPAPs), hyperbeanins P-Q (1-2), and two new biosynthetic precursors, hyperbeanins R-S (3-4), were isolated from Hypericum beanii, together with three known analogs (5-7). Compound 1 was one of type A PPAPs featured with unusual bicyclo[5.3.1]hendecane core. The structures of isolates were established by NMR spectroscopic methods, experimental electronic circular dichroism (ECD) spectra and comparisons with known compounds. Compounds 5 and 6 showed obvious hepatoprotective activity at 10 µM against paracetamol-induced HepG2 cell damage.


Assuntos
Hypericum , Humanos , Hypericum/química , Floroglucinol , Estrutura Molecular , Células Hep G2 , Espectroscopia de Ressonância Magnética
3.
Zhongguo Zhong Yao Za Zhi ; 46(15): 3859-3864, 2021 Aug.
Artigo em Chinês | MEDLINE | ID: mdl-34472260

RESUMO

This study explored the chemical constituents of the aerial part of Hypericum curvisepalum. Sixteen compounds were isolated from the 95% ethanol extract of H. curvisepalum with various chromatographic techniques, including a new prenylated phenyl polyketide, mysorenone D(1). Other compounds were mysorenone-A(2), mysorenone-C(3), mysorenone-B(4), peplidiforone A(5), 4-methoxy-3-(2-methylbut-3-en-2-yl)-6-phenyl-2H-pyran-2-one(6), hyperenone-A(7), 4-(3,3-dimethylallyl)oxy-6-phenyl-α-pyrone(8), peplidiforone B(9), elegaphenone(10), hypercohin A(11), hyperisampsin G(12), spathulenol(13), quercetin(14), ß-sitosterol(15), and ß-amyrin(16).


Assuntos
Hypericum , Benzofenonas , Quercetina
4.
Huan Jing Ke Xue ; 40(10): 4450-4460, 2019 Oct 08.
Artigo em Chinês | MEDLINE | ID: mdl-31854812

RESUMO

The relationships between inflow and outflow water quality data for Poyang Lake from 1996 to 2016 are discussed and the main influencing factors are identified. TN and TP were the main factors causing a decline in water quality in Poyang Lake during the study period. The water quality of both the inflow and outflow rivers was generally good between 1996 and 2003; however, water quality declined over the study period, which is attributed to an increase in nutrients loads in the watershed. From 2004 to 2011, the water quality of the "Five Rivers" decreased significantly, which caused the water quality of Poyang Lake to decline. Due to the high purification capacity of Poyang Lake, the water quality of the outflow during this period was relatively good. A decline in water quality after this point was affected by pollution loads and hydrological conditions. Specifically, from 2012 to 2016, water quality in Poyang Lake and of the inflow water declined further. This was combined with a decrease in the water-purification capacity of the lake due to changes in the hydrological conditions, resulting in lower water quality at the outflow. Overall, the water quality of the inflow river has been closely related to the water quality in Poyang Lake. The concentrations of TN were significantly higher in the southern and eastern areas of Poyang Lake compared to the western areas. Higher nutrient loading from the Ganjiang River and the Xinjiang River has been an important driver. The concentrations of TP in the southern area of the lake have been significantly higher than in the eastern and western areas. This is attributed to comparatively high TP loads in the Ganjiang River and the Fuhe River. Compared to the changes in hydrological conditions, variations in nutrient loading have had a greater effect on water quality in the lake.

5.
Zhongguo Zhong Yao Za Zhi ; 41(17): 3260-3264, 2016 Sep.
Artigo em Chinês | MEDLINE | ID: mdl-28920380

RESUMO

To study the chemical constituents of the aerial parts of Myripnois dioica. Twelve compounds were separated from the 95% ethanol extract of M. dioica by using various chromatographic techniques. Their stuctures were identified on the basis of their physicochemical properties and spectral data as 8-desoxyurospermal A(1), zaluzanin C(2), dehydrozaluzanin C(3), glucozaluzanin C(4), macrocliniside B(5), macrocliniside I(6), taraxinic acid-14-O-ß-D-glucopyranoside(7), ainsliaside B(8), apigenin(9), luteolin(10), apigenin-7-O-ß-D-glucopyranoside(11), and luteolin-7-O-ß-D-glucopyranoside(12). Except for compound 8, the other compounds were isolated from this genus for the first time. Compound 8 was found to decrease blood glucose level properly in alloxan-induced diabetic mice.


Assuntos
Asteraceae/química , Flavonoides/análise , Animais , Apigenina/análise , Diabetes Mellitus Experimental/tratamento farmacológico , Glucosídeos , Luteolina/análise , Camundongos , Compostos Fitoquímicos/análise
6.
Zhong Xi Yi Jie He Xue Bao ; 10(5): 569-76, 2012 May.
Artigo em Chinês | MEDLINE | ID: mdl-22587980

RESUMO

OBJECTIVE: To investigate the effects of the effective component group of Xiaoxuming Decoction (XXM), a compound traditional Chinese herbal medicine, on cerebral mitochondria in rats with chronic cerebral ischemia. METHODS: Rats were subjected to permanent bilateral common carotid artery occlusion to induce chronic cerebral ischemia. Then, the rats with chronic cerebral ischemia were randomly divided into five groups: model group, extract of Ginkgo biloba group and low-, medium- and high-dose effective component group of XXM groups. Another 11 rats without common carotid artery occlusion were used as a sham control. Gradient centrifugation was used to obtain the mitochondria from the rat brain. Clark oxygen electrode method was used to determine mitochondrial respiratory function. Photometric determination was used to measure mitochondrial swelling. Rodamine 123 was used to measure mitochondrial membrane potential. Western blotting was used to detect mitochondrial apoptosis. RESULTS: Compared with the sham group, the mitochondria dysfunction was caused by chronic cerebral ischemia associated with the decrease of oxidative phosphorylation parameters and the mitochondrial membrane potential, the increase of the mitochondrial degree, the elevation of reactive oxygen species level, the decrease in Bcl-2/Bax ratio, and the release of cytochrome c. The effective component group of XXM could reduce mitochondrial damage induced by chronic cerebral ischemia by improving the indexes mentioned above. CONCLUSION: The effective component group of Xiaoxuming Decoction can protect brain mitochondrial homeostasis and improve the function of mitochondria in rats with chronic cerebral ischemia, which may be the mechanism of its protection against chronic cerebral ischemia.


Assuntos
Isquemia Encefálica/metabolismo , Medicamentos de Ervas Chinesas/farmacologia , Mitocôndrias/efeitos dos fármacos , Animais , Isquemia Encefálica/prevenção & controle , Medicamentos de Ervas Chinesas/uso terapêutico , Masculino , Potencial da Membrana Mitocondrial/efeitos dos fármacos , Mitocôndrias/metabolismo , Ratos , Ratos Wistar , Proteína X Associada a bcl-2/metabolismo
7.
Atherosclerosis ; 222(1): 50-8, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22387061

RESUMO

OBJECTIVE: Because myocardial infarction is a major cause of morbidity and mortality worldwide, protecting the heart from the ischemia is the focus of intense research. Coptisine is an isoquinoline alkaloid extracted form Coptidis Rhizoma. This study aims to elucidate if coptisine is responsible for cardioprotection using myocardial infarction (MI) rat models and investigate its potential mechanism of action. METHODS: Myocardial infarction was produced in rats with 85 mgkg(-1) isoproterenol administered subcutaneously twice at an interval of 24 h. The rats were randomized into 7 groups: (I) Normal; (II) ISO; (III) ISO+fasudil; (IV) ISO+isosorbide dinitrate (ISDN) and (V-VII) ISO+coptisine (25, 50 and 100 mgkg(-1)). Cardiac function and markers of cardiac ischemic were assessed after MI. RESULTS: Rats pretreated with coptisine (25, 50 and 100 mgkg(-1)) for 21 days and received subcutaneously injected with ISO (85 mgkg(-1)) on the 20th and 21st day at an interval of 24 h. The results suggested that coptisine has strong antioxidant activity, and it can maintain cell membrane integrity, ameliorate mitochondrial respiratory dysfunction, reduce myocardial cells apoptosis, inhibit RhoA/ROCK expression induced by high-dose isoproterenol administration. CONCLUSIONS: Coptisine provided cardioprotection in a model of myocardial infarction, and therefore should be considered as a novel adjunctive therapy for attenuating myocardial damage.


Assuntos
Berberina/análogos & derivados , Cardiotônicos/uso terapêutico , Infarto do Miocárdio/prevenção & controle , 1-(5-Isoquinolinasulfonil)-2-Metilpiperazina/análogos & derivados , 1-(5-Isoquinolinasulfonil)-2-Metilpiperazina/farmacologia , Animais , Antioxidantes/farmacologia , Apoptose/efeitos dos fármacos , Berberina/uso terapêutico , Isoproterenol , Masculino , Mitocôndrias Cardíacas/efeitos dos fármacos , Infarto do Miocárdio/induzido quimicamente , Ratos , Ratos Sprague-Dawley , Quinases Associadas a rho/antagonistas & inibidores , Proteína rhoA de Ligação ao GTP/antagonistas & inibidores
8.
Eur J Pharmacol ; 674(2-3): 227-33, 2012 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-21996316

RESUMO

Baicalein is one of the major flavonoids obtained from the Scutellaria root. Previous pharmacological studies found that baicalein had neuroprotective effects in animal models of Parkinson's disease. The purpose of this paper was to explore the molecular mechanism of the action of baicalein on PC12 cells and isolated rat brain mitochondria. Firstly, we investigated the effects of baicalein on rotenone-induced toxicity in PC12 cells. The results showed that baicalein suppressed rotenone-induced apoptosis, and inhibited the accumulation of reactive oxidant species, ATP deficiency, mitochondrial membrane potential dissipation, and caspase-3/7 activation in a concentration-dependent manner, indicating that baicalein likely improved mitochondrial function. Furthermore, we used isolated rat brain mitochondria to evaluate the effect of baicalein. Treatment with baicalein prevented rotenone-induced reactive oxidant species production, ATP deficiency and mitochondrial swelling in isolated brain mitochondria. Interestingly, exposure of isolated mitochondria to baicalein promoted mitochondrial active respiration. These results suggest that baicalein may be a mitochondria-targeted antioxidant and exerts neuroprotective effects on rotenone-induced neurotoxicity. This study supports our previous research that baicalein possesses neuroprotective activity in vivo and it is worthy of further study.


Assuntos
Encéfalo/citologia , Citoproteção/efeitos dos fármacos , Flavanonas/farmacologia , Mitocôndrias/efeitos dos fármacos , Fármacos Neuroprotetores/farmacologia , Neurotoxinas/toxicidade , Rotenona/toxicidade , Animais , Apoptose/efeitos dos fármacos , Caspase 3/metabolismo , Caspase 7/metabolismo , Respiração Celular/efeitos dos fármacos , Masculino , Potencial da Membrana Mitocondrial/efeitos dos fármacos , Mitocôndrias/metabolismo , Dilatação Mitocondrial/efeitos dos fármacos , Estresse Oxidativo/efeitos dos fármacos , Células PC12 , Ratos , Ratos Sprague-Dawley
9.
Pharmacol Biochem Behav ; 98(2): 286-91, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21262257

RESUMO

Many studies of Parkinson's disease suggest that oxidative stress is involved in the neurodegenerative process. Baicalein has been shown to have antioxidant effects. The present study examines the effect of baicalein on 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced neurotoxicity in C57BL/6 mice. MPTP treatment impaired spontaneous motor activity and rotarod performance, but baicalein improved this deficit. Moreover, baicalein at 280 and 560 mg/kg exhibited a protective effect against the MPTP-induced decrease in tyrosine hydroxylase (TH)-positive fibers in the substantia nigra, demonstrated by the immunohistological, morphological and behavioral outcomes. MPTP treatment also decreased dopamine levels in the striatum. However, treatment with baicalein attenuated these decreases in dopamine levels by changing dopamine catabolism and inhibiting dopamine turnover. The neuroprotective effect of baicalein on dopaminergic neurons may partly be due to its antioxidant properties. Therefore, we speculate that baicalein might be a promising candidate for prevention or treatment of oxidative stress-related neurodegenerative disorders such as Parkinson's disease.


Assuntos
Encéfalo/efeitos dos fármacos , Flavanonas/farmacologia , Intoxicação por MPTP/prevenção & controle , Animais , Antioxidantes/farmacologia , Comportamento Animal/efeitos dos fármacos , Encéfalo/fisiopatologia , Corpo Estriado/efeitos dos fármacos , Corpo Estriado/metabolismo , Dopamina/metabolismo , Glutationa Peroxidase/metabolismo , Intoxicação por MPTP/fisiopatologia , Intoxicação por MPTP/psicologia , Masculino , Malondialdeído/metabolismo , Camundongos , Camundongos Endogâmicos C57BL , Neurônios/efeitos dos fármacos , Neurônios/patologia , Estresse Oxidativo/efeitos dos fármacos , Substância Negra/efeitos dos fármacos , Substância Negra/enzimologia , Substância Negra/patologia , Superóxido Dismutase/metabolismo , Tirosina 3-Mono-Oxigenase/metabolismo
10.
Eur J Pharmacol ; 627(1-3): 99-105, 2010 Feb 10.
Artigo em Inglês | MEDLINE | ID: mdl-19857483

RESUMO

Processes of synaptic plasticity, such as long-term potentiation (LTP), has been considered a cellular correlate of learning and memory and many neurological disorders accompanied by cognitive deficits exhibit abnormal synaptic function. This emerging concept is exemplified by Alzheimer's disease. Mounting evidence suggests that Alzheimer's disease begins with subtle alterations of hippocampal synaptic efficacy prior to frank neuronal degeneration, which make it critical to identify LTP enhancers to slow down or stop the progression of Alzheimer's disease. In this study, we found flavonoid luteolin could enhance basal synaptic transmission and facilitate the induction of LTP by high frequency stimulation in the dental gyrus of rat hippocampus. Furthermore, we investigated the effects of luteolin on chronic cerebral hypoperfusion-induced spatial learning dysfunction and LTP impairment in rat. The results showed chronic cerebral hypoperfusion produced by 2-vessel occlusion significantly impaired spatial learning and memory, and luteolin reversed the learning and memory deficit. 2-vessel occlusion resulted in dramatic inhibition of LTP formation in the hippocampus and luteolin significantly rescued the LTP impairment. These results demonstrate that luteolin not only directly modulates LTP formation, but also protects synapses from the detrimental effects of chronic cerebral hypoperfusion on LTP formation, which may contribute to the protective effects of luteolin on learning and memory. By immunoblotting, we found the effects of luteolin on LTP and memory may due to the activation of cAMP response element-binding protein (CREB). Therefore, flavonoid luteolin shows great potential as a novel treatment agent for protecting synaptic function and enhancing memory in neurodegenerative disorders.


Assuntos
Encéfalo/irrigação sanguínea , Encéfalo/efeitos dos fármacos , Circulação Cerebrovascular , Cognição/efeitos dos fármacos , Cognição/fisiologia , Potenciação de Longa Duração/efeitos dos fármacos , Luteolina/farmacologia , Animais , Comportamento Animal/efeitos dos fármacos , Comportamento Animal/fisiologia , Encéfalo/fisiologia , Encéfalo/fisiopatologia , Proteína de Ligação ao Elemento de Resposta ao AMP Cíclico/metabolismo , Hipocampo/efeitos dos fármacos , Hipocampo/metabolismo , Masculino , Aprendizagem em Labirinto/efeitos dos fármacos , Aprendizagem em Labirinto/fisiologia , Memória/efeitos dos fármacos , Memória/fisiologia , Doenças Neurodegenerativas/metabolismo , Doenças Neurodegenerativas/patologia , Doenças Neurodegenerativas/fisiopatologia , Neurônios/citologia , Neurônios/efeitos dos fármacos , Neurônios/patologia , Fosforilação/efeitos dos fármacos , Ratos , Ratos Sprague-Dawley , Transmissão Sináptica/efeitos dos fármacos , Fatores de Tempo
11.
Brain Res ; 1249: 212-21, 2009 Jan 16.
Artigo em Inglês | MEDLINE | ID: mdl-18977207

RESUMO

This study investigated the effects of baicalein, a natural compound isolated from the root of scutellaria, on cognitive and motor ability impaired by chronic cerebral hypoperfusion in rats, as well as its effects on brain mitochondria. Rats subjected to permanent bilateral common carotid artery occlusion experienced cognitive deficits, oxidative stress and mitochondria dysfunction, which was associated with the elevation of reactive oxygen species level, the decrease of oxidative phosphorylation parameters, the loss of mitochondrial membrane potential, the reduce in Bcl-2/Bax ratio, and the release of cytochrome c. Baicalein alleviated cognitive and motor impairments and decreased mitochondria reactive oxygen species production, in accordance with its improvements on membrane potential level, oxidative phosphorylation process, mitochondrial swelling degree, Bcl-2/Bax ratio and cytochrome c release. These data indicated that baicalein might have therapeutic potential for the treatment of dementia caused by chronic cerebral hypoperfusion, contributed to its protections on brain mitochondrial homeostasis and function.


Assuntos
Encéfalo/fisiopatologia , Transtornos Cerebrovasculares/fisiopatologia , Flavanonas/farmacologia , Mitocôndrias/fisiologia , Estresse Oxidativo/efeitos dos fármacos , Animais , Western Blotting , Encéfalo/efeitos dos fármacos , Artérias Carótidas , Transtornos Cerebrovasculares/metabolismo , Cognição/efeitos dos fármacos , Cognição/fisiologia , Citocromos c/metabolismo , Masculino , Potencial da Membrana Mitocondrial/efeitos dos fármacos , Mitocôndrias/efeitos dos fármacos , Dilatação Mitocondrial/efeitos dos fármacos , Atividade Motora/efeitos dos fármacos , Fosforilação Oxidativa/efeitos dos fármacos , Proteínas Proto-Oncogênicas c-bcl-2/metabolismo , Ratos , Ratos Wistar , Espécies Reativas de Oxigênio/metabolismo , Proteína X Associada a bcl-2/metabolismo
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