Mercurous Chloride Catalyzed Mannich Condensation of Terminal Alkynes with Secondary Amines and Aldehydes

Mercurous chloride catalyzed Mannich condensation of terminal alkynes with secondary amines and aldehydes has been developed. The reaction generated β-aminoalkynes in good yields.

建立因特网上的邮件服务器

主要介绍了Ｗｉｎｄｏｗｓ操作系统下如何用ＭＥＲＣＵＲ３．０建立因特网上的邮件服务器，具体介绍了邮件服务器软件的安装、配置，用户邮箱的建立，用户用邮件来更改口令，以及自动回复器的设定。

The Protective Role of Procyanidins and Lycopene Against Mercuric Chloride Renal Damage in Rats

Objective This study aims to investigate the protection of procyanidins and lycopene from the renal damage induced by mercuric chloride.Methods Rats were treated with either procyanidins or lycopene 2h before HgCl 2 subcutaneously injection,once daily treatment for 2 successive days.Results In comparison with HgCl 2 group,markers of renal function such as blood urea nitrogen in serum and urinary protein were decreased to （18.45±11.63） mmol/L and （15.93±9.36） mmol/L,（4.54±0.78） g/（g Cr） and （4.40±1.12） g/（g Cr）.N‐acetyl‐beta‐D‐glucosaminidase,lactate dehydrogenase,alkaline phosphatase in urine were depressed to （125.49±11.68） U/（g Cr）,（103.73±21.79） U/（g Cr）,（101.99±12.28） U/（g Cr）,and （113.19±23.74） U/（g Cr）,（71.14±21.80） U/（g Cr）,（73.64±21.51） U/（g Cr） in procyanidins and lycopene groups.Indicators of oxidative stress,for example,Glutathion was reduced to （45.58±9.89） μmol/（g pro） and （45.33±5.90） μmol/（g pro）,and antioxidant enzymes such as superoxide dismutase,glutathione‐peroxidase were enhanced to （43.07±10.97） U/（mg pro） and （39.94±6.04） U/（mg pro）,（83.85±18.48） U/（mg pro）,and （85.62±12.68） U/（mg pro）.Malondialdehyde was lowered to （0.95±0.12） （μmol/g pro） and （1.03±0.12） μmol/（g pro） in procyanidins and lycopene groups.ROS generation was decreased by 27.63% and 16.40% and apoptosis was also decreased in procyanidins and lycopene groups respectively.Pathological changes were much better as well.Conclusion Procyanidins and Lycopene play some protective role against mercury kidney damage.

Effect of Mercuric Compounds on Pine and Sycamore Germination and Early Survival

Mercury pollution has become an important current issue as a result of its environmental effects on a global scale. The Oak Ridge Reservation, established in 1942, was the designated site for the construction of the atomic bomb. During a 20-year period from 1944-1963 radioactive and toxic chemical pollutants, especially mercury compounds were released into the surrounding waterways.A germination study was conducted to investigate the ability of three tree species, American sycamore (Platanus occidentalis),shortleaf pine (Pinus echinata), and loblolly pine (Pinus taeda) seeds to germinate in mercuric nitrate (Hg(NO3)2 and methylmercury chloride (CH3HgCl) solutions. A subsequent greenhouse study was conducted to assess the phytotoxic effects of different mercuric solutions on Platanus occidentalis (American Sycamore), inoculated with soils from East Fork Poplar Creek.We also measured vegetation stress by Near Infrared (NIR) spectroscopy.The wavelengths examined were those thatare specific to chlorophyll and several carotenoids, which are involved in photosynthesis: 430 nm (Chl a), 448 nm (Chl b, carotenoids), 471 nm (carotenoids), 642 nm (Chl b), 662 & 680 nm (Chl a). Principal component analysis (PCA) was performed to identify patterns in sycamore leaf spectral data.Under in vitro conditions, as mercury concentration increased above 100 mg·kg-1, germination of all species decreased, with P. echinata being the least sensitive. Germination was inhibited more when seeds were exposed to methyl mercury chloride than to mercuric nitrate. Organic species of mercury proved to be more toxic than inorganic species of mercury in our greenhouse study. Significant changes occurred in levels of all pigments sampled (p430, p448, p471, p642, p662, and p680) over the course of the experiment. NIR spectroscopy was not sensitive enough to detect other chemical changes to foliage following mercury application.

Red onion extract(Allium cepa L.)supplementation improves redox balance in oxidatively stressed rats

Onions,consumed worldwide,are a good source of dietary phytochemicals with proven antioxidant properties.Catechin and quercetin are the most common and widely consumed flavonoids.The present study aimed to investigate the possible protective effect of onion extract as well as flavonoids(catechin and quercetin)on rats subjected to oxidative stress by mercuric chloride(HgCl2)treatment.Experiments were conducted on rat erythrocytes,which are a good model system to study oxidative stress.Results show that the oxidative stress induced by HgCl2 in Wistar rats resulted in substantially increased erythrocyte lipid peroxidation and higher activity of red cell plasma membrane redox system(PMRS)along with corresponding decrease in the intracellular reduced glutathione and antioxidant activity.Onion extract supplementation significantly(P<0.05)attenuated these adverse effects of HgCl2.Flavonoid supplementation resulted in a slightly higher antioxidant response compared to onion extract.We conclude that supplementation of these flavonoids results in normalization of erythrocyte PMRS activity which provides onion(rich in quercetin),a novel mechanism to exert its antioxidant effect against HgCl2-induced oxidative stress in rat erythrocytes in vivo.©2013 Beijing Academy of Food Sciences.Production and hosting by Elsevier B.V.All rights reserved.

Neuroprotection by Melatonin on Mercury Induced Toxicity in the Rat Brain

Free radicals are common outcome of normal aerobic cellular metabolism. In-built antioxidant system of body plays its decisive role in prevention of any loss due to free radicals. However, imbalanced defense mechanism of antioxidants and overproduction or incorporation of free radicals from environment to living systems leads to serious damage. It also attacks nervous system resulting in neural-degeneration. In order to evaluate the neurotoxic effect on the brain parts of mercury in our study, oxidative stress indices of enzymatic and non enzymatic components were measured in rats intoxicated with mercury (2 mg and 4 mg/kg body weight) for 60 days to adult rats. Along with gravimetry, tissue burden was also recorded. Alterations in these indices were further supported by ultrastructural studies carried out in the brain as indicated by myelin disintegration, cell organelle alterations and neuronal loss by mercury poisoning. Treatment with the antioxidant melatonin (N-acetyl 5-methoxy tryptamine, 5 mg/kg) prevented mercury exerted toxicity due to its antioxidant property. The pathological changes were also ameliorated in the brain region comparatively to support biochemical profile of brain. Thus, melatonin produced neuroprotection against mercury poisoning in rats.

Effect of Short-Term Exposure to Mercuric Chloride on the Air-Breathing Catfish,Heteropneustes fossilis──Ⅱ.Scanning Electron Microscopic Study of the Gill

Alterations in the respiratory epithelium of gills of a catfish, Heteropneustes fossilis by the sublethal and lethal concentrations of HgCl2 have been observcd using scanning electron microscope. Fish exposed to 0.1 ppm shows a thin coat ot mucus, but the continuous layer of mucus is not retained in 0.3 ppm after 24 h of exposure. Epithelial cells of the gill filament are hyperplastic. Other changcs in the respiratory epithelium are contraction of epithelium, formation of interlamellar bridge and diminishing number of microridges. Massive destruction of the respiratory epithelium by deep lesions and sloughing of epithelial layer in 0.5 and 1.0 ppm solutions after 6-12 h of exposure apparently causes death to the fish. SEM observations are well in conformity with the findings made at light microscopic level

Combined Effects of Cd and Hg on Liver and Kidney Histology and Function in Wistar Rats

The present study was performed in order to discern the effects of combined exposure to cadmium and mercury on liver function and histopathological alterations in male adult Wistar rats. In the present investigation, cadmium (100 mg/l) and mercury (25 mg/l) were administered orally for 10 weeks separately or in combination. The rational for studying cadmium and mercury is that both of these metals are encountered frequently in the same contaminated areas. In liver, the activities of serum alanine aminotransferase (ALT) and aspartate amino tranferase (AST) increased significantly in the cadmium (Cd) and mercury (Hg) alone or in combination (Cd + Hg) compared to the control suggesting that both cadmium and mercury cause hepatotoxicity spatially when co-administrated. We noted an increase in serum lactate dehydrogenase (LDH) activity in Cd and combined Cd + Hg treated groups while it decreased in Hg treated group. There was no statistically significant change in the level of total bilirubilin. Serum urea concentration showed a significant increase in the Cd and Hg groups compared to the control group. However an increase in serum creatinine concentration was noted only in the combined treated rats showing that renal insufficiency is more serious in the co-exposed group. Light microscopic examination indicated severe histological changes in the two organs under Cd and mercury influence. Results of the present investigation clearly showed that mercury has profound effects of hepatic handling of cadmium (synergistic effect) as shown by histological and biochemical results. Moreover, we observed a antagonist effect between these two toxic metals on kidney markers such as urea.

Effect of mercuric chloride on membrane-bound enzymes in rat testis

Aim: To study the effect of mercuric chloride on the membrane-bound enzymes. Methods: The effect of mercuric chloride at two different doses, 1 mg/kg (low dose) and 2 mg/kg (high dose), orally for 30 days, was observed on the membrane-bound enzymes in the testis of adult albino rats. Results: Mercuric chloride significantly decreased the body weight and testis weight in the high dose group (P<0.05), but not in the low dose group. The activities of 5' nucleotidase and adenosine triphosphatases were markedly decreased (P<0.01) in the testis of both groups. Alkaline phosphatase and γ-glutamyl transferase activities were significantly increased (P<0.01) in both groups. However, the effect was more pronounced in the high than in the low dose groups. Conclusion: The dose dependent effect of mercuric chloride on these enzymes may affect the membrane characteristics and thereby the fertility of the animal. (Asian J Androl 2002 Dec; 4:309-311)

Drought stress,mercuric chloride,andβ-mercaptoethanol effects on hydraulic characteristics of three cultivars of wolfberry(Lycium chinense)

In order to further understand the effects of drought stress on hydraulic characteristics and the relationship between hydraulic conductivity and aquaporins or water channels of root systems of three wolfberry cultivars(Lycium chinense Mill.),hydraulic conductivity of 2-yearold pot-grown seedlings was measured under drought stress,rewatering,and treatment with exogenous mercuric chloride andβ-mercaptoethanol.Under moderate and severe drought stress levels,the most significant decrease of hydraulic conductivity was 37.3%and 24.0%,respectively,in the‘Ningqi 5’cultivar compared with the nonstressed control.After rewatering,the rate of recovery in specific conductivity was most rapid in the‘Mengqi 1’cultivar,at 0.058 and 0.072 kg MPa^-1 m^-2 s^-1 h^-1 under moderate and severe drought stress levels,respectively.The‘Mengqi 1’cultivar had the highest recovery degree of hydraulic conductivity under two concentrations ofβ-ME(500 or 1000 lmol L^-1),reaching 82.4%and 88.5%,respectively,of the initial conductivity.The adaptive capacity of hydraulic conductivity in the‘Ningqi 5’cultivar was weaker than in the‘Ningqi 1’and‘Mengqi 1’cultivars under drought stress.The recovery capacity of hydraulic conductivity in‘Mengqi 1’cultivar was stronger than the‘Ningqi 1’and‘Ningqi 5’cultivars after rewatering.Aquaporins of the‘Ningqi 1’cultivar root systems had the highest binding affinity with mercuric chloride,which was the most likely cause in the decrease in hydraulic conductivity,whereas aquaporins of‘Mengqi 1’root systems had the weakest binding affinity.The inhibitory effect of mercuric chloride was readily eliminated byβ-mercaptoethanol in the‘Mengqi 1’cultivar.The hydraulic characteristics of this cultivar were more sensitive to drought,mercuric chloride andβ-mercaptoethanol than the other cultivars.

Properties of mercuric reductase from a HgCl_2-resistant fungus

ＰｒｏｐｅｒｔｉｅｓｏｆｍｅｒｃｕｒｉｃｒｅｄｕｃｔａｓｅｆｒｏｍａＨｇＣｌ＿２－ｒｅｓｉｓｔａｎｔｆｕｎｇｕｓＷａｎｇＢａｏｊｕｎ；ＬｉＷｅｎｚｈｏｎｇ；ＹａｎｇＨｕｉｆａｎｇＩｎｓｔｉｔｕｔｅｏｆＭｉｃｒｏｂｉｏｌｏｇｙ，ＣｈｉｎｅｓｅＡｃａｄｅ...

PROTECTIVE EFFECTS OF CALCIUM ANTAGONIST ON VASCULAR SYSTEM AGAINST TOXICITY INDUCED BY MERCURIC CHLORIDE

Objective To explore the toxic effects of mercuric chloride (HgCl 2) on vascular smooth muscle as well as its relationship to calcium antagonist. Methods By using isolated vascular tension methods, we studied the effect of HgCl 2 on isolated rabbit aortic rings. Results HgCl 2 (1-100 μmol·L -1) caused a concentration-dependent contraction of rabbit aortic rings, which did not change with phentolamin or without endothelium. In KH solution with Ca 2+ , the maximum contraction amplitude reduced by(61.2±3.3)%. Nifedipine produced a concentration-dependent decrease of the maximum contraction amplitude. Conclusion Calcium antagonist has protective effects on vascular smooth muscle against damage induced by HgCl 2.

Time Dependent Distribution of [^(203)Hg] Mercuric Nitrate in the Subcellular Fractions of Rat and Fish Liver

Cytotoxicity of inorganic mercury to the liver of two species, Anabas tesludineus and Sprague Dawley male rat was evaluated. Distribution kinetics of this metal in the different hepatic subcellular fractions were followed for 48 h after a single injection of [203Hg] mercuric nitrate at a dose of 4mg/kg b.w. Interaction of this metal with protein, DNA and RNA was also studied. In rat, nuclear and lysosomal fractions showed a significant increase in the protein content, while in fish, the amount of protein increased in all fractions except microsome. Comparatively more mercury was bound to protein in fish during the later phase of treatment. Retention of mercury in nuclear DNA of rat gradually declined from 15 min to 48 h of treatment, while, mitochondria! DNA binding to mercury increased from 15 min to 2 h of post injection and then declined in the later phase of the experiment. Such a biphasic binding pattern of mercury was shown by both the nuclear and mitochondrial DNA of the fish. The nuclear RNA of rat and mitochondrial and cytosolic RNA of both test species also showed a biphasic pattern of mercury binding, however, with a higher rate of binding in fish at the later phase of the experiment. The present study thus highlights that (a) mercury follows a definite distribution pattern in the subcellular fractions of the liver in both animal species, (b) cytosol is the major site of mercury accumulation.

STUDIES ON THE PROPERTIES OF SCHIFF BASE TYPE ARYLMERCURY COMPOUNDS.II ^(199)Hg NMR SPECTRA OF MERCURATED DERIVATIVES OF SUBSTITUTED BENZYLIDENEANILINES

^(199)Hg NHR spectra of 18 Schiff base type arylmercury compounds have been studied.It was further confirmed that in the molecule of XC_6H_4CH=NC_6H_3-2-HgC1-4-CH_3 there exists an intramolecular N→Hg coordination via a four-membered ring.For the series of XC_6H_4CH=NC_6H_3-2-HgCl-4-CH_3(X is a para-or mera-substituent),there is a good linear correlation between δ^(199)Hg and Hammett's o constants.The influence of substituents of C-pheny1 ring on the δ ^(199)Hg can be explained in terms of the intramolecular N→Hg coordination.

Effect of Short-Term Exposure to Mercuric Chloride on the Air-Breathing Catfish,Heteropneustes fossilis──Ⅰ.Light Microscopic Study of the Gill

Histopathological effects of sublethal (0.1, 0.2, 0.3 ppm) and lethal (0.5, 1.0 ppm)solutions of mercuric chloride (HgCl2) have been studied on the gills of the air breathing catfish, Heteropneustes fossilis at the intervals ranging from 6h to 15 days. Thickening of the epithelium, swelling and hyperplasia of the mucous cells, fusion of secondary lamellae, formation of interlamellar bridge and deposition of mucous over the entire surface are some noteworthy features of mercury poisoning in sublethal concentrations. Acute pathological manifestations are formation of subepithelial space, sloughing of the epithelial layer, hemorrhage and hypertrophy of the mucous cells. Causes and impact of these cellular alterations affecting survival of the fish have been discussed

Acute Toxic Effects of Mercuric Chloride on the Mucocytes of the Epithelial Lining of the Accessory Respiratory Organ and Skin of the Air Breathing Catfish Heteropneustes fossilis（Bloch）^1

Acute toxicity of 0.3 ppm mercuric chloride on the mucocytes of the branchial diverticulum and skin of Heteropneustes fossilis results in cyclic increases followed by decreases in the density, area occupancy and volume at different intervals of exposure. The alterations in the two tissues do not follow the same path perhaps due to different modes of action of the mercury salt: The skin comes under direct contact effects, while the branchial diverticulum may be affected by hormonal imbalance caused by a stress effect.

Effect of Mercuric Chloride and Cadmium Chloride on Gonadal Function and Its Regulation in SexuallyMature Common Carp Cyprinus carpio

Gonadal function in fish, CJprinus carpio was significantly affected by sublethal doses of mercuric chloride (HgCl2 ) and cadmium chloride (CdCl2 ) in chronic (45 days ) exposure.Parameters investigated were nonesterified (NE) and esterified (E) cholestcrol of ovary,liver and serum and ovarian 3β-Hydroxysteroid and 17β-Hydroxysteroid dehyrogenaseenzyme activity and serum and pituitary gonadotropin (GtH) levels. Both the pollutantswere able to reduce the hypothalamic extract (HE) or gonadotropin releasing hormone(GnRH) induced pituitary GtH release in vitro. Short term (96h) exposure of the fish tothe pollutants had no significant effect on the gonadal function. ln addition to thedeleterious effect of pollutants on the gonadal steroidogenesis and pituitary gonadotropin release, using [4-14C] cholesterol as a tracer it was found that for 45 days expeure, HgCl2'had an adverse effect on the transport of cholesterol from circulation to ovary.

Histopathological Changes in the Epidermis of the Air Breathing Catfish Heteropneustes fossilis Exposed to Sublethal Concentration of Mercuric Chloride

Histopathological alterations induced by the sublethal concentration of (0.03 ppm) mercuric chloride solution on the epidermis of the fresh-water catfish Heteropneuates fossilis have been studied. It induces slow but significant histopathological changes in the various cellular components of the epidermis. It induces vacuolization, necrosis and pycnosis of the nuclei of the epithelial cells which subsequently shed. Loosening of epithelial cells of the outermost and middle layers following degeneration of the intercellular material and widened intercellular spaces is another important alteration. Prolonged mercury treatment also causes a gradual decrease in staining intensity for sulphated glycosaminoglycans in the outer border of the most superficial layer epithelial cells. The glandular elements (club cells and mucocytes) also get affected, showing cyclic degeneration followed by regeneration.

Determination of Mercuric Ion in Water Samples with a LED Exciting and CCD Based Portable Spectrofluorimeter

The fluorescent characteristics of a fluorimetric chemosensor for mercuric ion, Hg2+, employing a synthesized Rhodamine 6G derivative, have been analyzed. For that, a portable spectrofluorimeter composed of a 515 nm LED as excitation source, two fiber-optics and a CCD camera as detector, has been used, intended for “in situ” analysis. A highly selective Rhodamine based probe for Hg2+, that is water soluble and gives a positive response upon analyte binding, is reported. The reagent is bearing a monothiospirolactone group in a Rhodamine 6G architecture and the thiol atom served for the direct attack of thiophilic Hg2+. The fluorescence enhancement is attributed to the spirolactone ring opening and the coordination of two sulphur atoms to Hg2+ giving a 2:1 reagent: Hg2+ stoichiometry complex.