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1.
Acta cir. bras ; 35(5): e202000507, 2020. graf
Article in English | LILACS | ID: biblio-1130640

ABSTRACT

Abstract Purpose To develop a new wound dressing composed of alginate and Aloe vera gel and cross-linked with zinc ions. Methods The aloe-alginate film was characterized using scanning electron microscopy (SEM), swelling profile, mechanical properties, polysaccharide content and X-ray diffraction (XRD). Thirty Wistar rats were divided in two groups a) treated with aloe-alginate film and b) control (treated with sterile gauze). Wound contraction measurements and hystological analysis were performed on 7th, 14th and 21st days after wound surgery. Results The aloe-alginate film presented adequated mechanical resistance and malleability for application as wound dressing. There was no statistical difference in wound contraction between two groups. Histological assay demonstrated that aloe-alginate film presented anti-inflammatory activity, stimulated angiogenesis on proliferative phase and a more significant increased in collagen type I fibers and decreased type III fibers which promoted a mature scar formation when compared to control. Conclusions The aloe-alginate film showed adequate physicochemical characteristics for wound dressing applications. The in vivo assay demonstrated that aloe-alginate film enhanced the healing process of incisional skin wounds.


Subject(s)
Animals , Rats , Wound Healing/drug effects , Chlorides/pharmacology , Chlorides/chemistry , Zinc Compounds/pharmacology , Zinc Compounds/chemistry , Plant Preparations/pharmacology , Alginates/pharmacology , Aloe , Rats, Wistar
2.
Salud pública Méx ; 56(6): 660-665, nov.-dic. 2014.
Article in Spanish | LILACS | ID: lil-733346

ABSTRACT

Este artículo fue concebido para analizar la función de la Escuela de Salud Pública de México (ESPM) desde el año 2000 hasta el presente. Uno de sus puntos centrales es el análisis del proceso de reorientación de la labor educativa de la escuela con la finalidad de responder a los retos en materia de salud y educación surgidos a finales del siglo XX. Para exponer cómo ha evolucionado dicho proceso, retomamos tres ejes rectores que caracterizan la labor de la escuela en la actualidad: el cambio de modelo pedagógico, la incorporación de las tecnologías de la información y las comunicaciones, y la profesionalización de la docencia. Con la exposición de este tema, y a través del contraste entre el pasado y el presente, buscamos completar la historia de trabajo ininterrumpido de la Escuela durante sus 92 años de existencia, que ha trascendido los confines del país.


This article was conceived to analyze the work of the School of Public Health of Mexico (ESPM for is acronym in Spanish) from the year 2000 to the present day. One of the highlights that we will examine is the reorientation of the educational work of the school in order to meet the challenges in health and education that emerged during the end of the twentieth century. In order to explain the evolution of this process, we will describe the three main guiding principles that characterize the present work of the school: the pedagogical model's change, the incorporation of the information and communication technologies, and the professionalization in teaching. The purpose of this work is to define those guiding principles, and to expose, through the contrast between past and present, the complete history of uninterrupted work of the School of Public Health of Mexico during its ninety-two years of existence, that has gone beyond the boundaries of the country.


Subject(s)
Animals , Female , Humans , Mice , Cysteine Endopeptidases/metabolism , Mengovirus/enzymology , Viral Proteins , Amino Acid Sequence , Antibodies, Monoclonal/metabolism , Antibodies, Viral/metabolism , Capsid/metabolism , Chlorides/pharmacology , Cysteine Endopeptidases/genetics , Enzyme Inhibitors/pharmacology , Ethylmaleimide/pharmacology , HeLa Cells , Iodoacetamide/pharmacology , Leucine/analogs & derivatives , Leucine/pharmacology , Mice, Inbred BALB C , Molecular Sequence Data , Peptides/chemical synthesis , Peptides/metabolism , Protein Precursors/metabolism , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Substrate Specificity , Zinc Compounds/pharmacology
3.
West Indian med. j ; 61(2): 122-127, Mar. 2012. ilus, graf
Article in English | LILACS | ID: lil-672868

ABSTRACT

OBJECTIVE: Alzheimer s disease and Parkinson s disease are two of several neurodegenerative disorders that affect the elderly. Although their aetiology remains uncertain, studies suggest that elevated aluminium or other metal ions in the brain directly influence the development of the histological abnormalities normally associated with these diseases; other investigations suggest that metal-ion-induced-dysfunction of mitochondria might be a critical factor. METHODS: In this study, the impact of elevated aluminum (Al3+), ferric (Fe3+), calcium (Ca2+) and magnesium (Mg2+) ions on brain histology and on the protein composition of brain mitochondria were evaluated. Rabbits were injected intra-cerebrally with 1.4% solutions of either aluminium chloride (AlCl3), ferric chloride (FeCl2), calcium chloride (CaCl2) or magnesium chloride (MgCl2) and sacrificed 10 days later. RESULTS: Histological analysis revealed that Al3+ but not the other ions induced neurofibrillary degeneration within the midbrain and medulla. Alternatively, SDS-PAGE revealed that Fe3+, Ca2+ and Mg2+ but not Al3+ induced alterations to the distribution of brain mitochondrial proteins. Both Fe3+ and Ca2+ triggered decreased concentration of three low molecular weight proteins (~7-14 kd) but Ca precipitated their total absence. Both ions led to increased concentration of a high molecular weight protein (~ 110 kd). In contrast, Mg2+ led to the total absence of the protein of lowest molecular weight (~7 kd) and increased concentration of a ~36 kd protein. CONCLUSION: These results suggest that elevation of some metal ions in the brain induces protein aggregation with the nature of the aggregation being highly ion dependent. The results also point toward major differences between the histopathological effect of Al3+ and other ions.


OBJETIVO: La enfermedad de Alzheimer y la enfermedad de Parkinson son dos de los varios trastornos neurodegenerativos que afectan al anciano. Aunque su etiologia sigue siendo incierta, los estudios sugieren que el aumento de los iones de aluminio, influyen directamente sobre el desarrollo de las anormalidades histológicas asociadas normalmente con estas enfermedades. Otras investigaciones sugieren que la disfunción de las mitocondrias, inducida por iones metálicos, pudiera ser un factor critico. MÉTODOS: Este estudio evalúa el impacto del aumento de los iones de aluminio (Al3+), los iones férricos (Fe3+), y los iones de calcio (Ca2+) y magnesio (Mg2+) sobre la histologia del cerebro y la composición proteica de las mitocondrias del cerebro. Un número de conejos recibieron inyecciones intracerebrales de soluciones al 1.4% de soluciones de cloruro de aluminio (AlCl3), cloruro ferroso (FeCl3), cloruro de calcio (CaCl2), o cloruro de magnesio (MgCl2), y fueron sacrificados después de 10 días. RESULTADOS: El análisis histológico reveló que el Al3+ indujo una degeneración neurofibrilar dentro del mesencéfalo y la médula, Sin embargo, esto no ocurrió con los otros iones. Alternativamente, la técnica de electroforesis SDS-PAGE reveló que los iones Fe3+, Ca2+ y Mg2+, a diferencia del ión Al3+, inducían alteraciones de la distribución de las proteínas mitocondriales cerebrales. Tanto el Fe3+ como el Ca2+ desencadenaron una disminución de la concentración de tres proteínas de bajo peso molecular (~7-14 kd) pero Ca2+ precipitó su ausencia total. Ambos iones condujeron a un aumento de una proteína de peso molecular alto (~ 110 kd). En cambio, Mg2+ llevó a la ausencia total de la proteína de más bajo peso molecular (~7 kd) y al aumento de la concentración de una proteína de ~36 kd. CONCLUSIÓN: Estos resultados parecen sugerir que la elevación de algunos iones de metal en el cerebro induce la agregación de la proteína, siendo la naturaleza de la agregación altamente dependiente de los iones. Los resultados también apuntan a grandes diferencias entre el efecto histopatológico del Al3+ y otros iones.


Subject(s)
Animals , Rabbits , Brain/metabolism , Calcium Chloride/pharmacology , Chlorides/pharmacology , Ferric Compounds/pharmacology , Magnesium Chloride/pharmacology , Mitochondrial Proteins/metabolism , Aluminum Compounds/pharmacology , Brain/ultrastructure , Electrophoresis, Polyacrylamide Gel , Mitochondrial Proteins/drug effects
4.
Indian J Biochem Biophys ; 2011 Oct; 48(5): 331-335
Article in English | IMSEAR | ID: sea-135336

ABSTRACT

Biosynthesis of gold nanoparticles by Streptomycetes from Himalayan Mountain was undertaken for the first time. Out of 10 actinomycete strains tested, four strains (D10, HM10, ANS2 and MSU) showed evidence for the intracellular biosynthesis of gold nanoparticles, among which the strain HM10 showed high potency. Presence of spherical and rod shaped gold nanoparticles in mycelium of the strain HM10 was determined by transmission electron microscopy (TEM) and X-ray diffraction analysis. The average particle size ranged from 18-20 nm. UV spectral analysis indicated that the reduction of chloroauric acid (HAuCl4) occurred within 24 h of reaction period. Further, the strain HM10 showed enhanced growth at 1 and 10 mM concentration of HAuCl4. The gold nanoparticles synthesized by the strain HM10 showed good antibacterial activity against S. aureus and E. coli in well-diffusion method. The potential actinomycete HM10 strain was phenotypically characterized and identified as Streptomyces viridogens (HM10). Thus, actinomycete strain HM10 reported in this study is a newly added source for the biosynthesis of gold nanoparticles.


Subject(s)
Actinobacteria/metabolism , Anti-Bacterial Agents/biosynthesis , Anti-Bacterial Agents/chemistry , Chlorides/chemistry , Chlorides/metabolism , Chlorides/pharmacology , Escherichia coli/drug effects , Gold Compounds/chemistry , Gold Compounds/metabolism , Gold Compounds/pharmacology , Microscopy, Electron, Transmission/methods , Nanoparticles/chemistry , Nanotechnology/methods , Staphylococcus aureus/drug effects , Streptomyces/metabolism , X-Ray Diffraction
5.
Journal of Korean Medical Science ; : 57-62, 2007.
Article in English | WPRIM | ID: wpr-226405

ABSTRACT

This study was designed to identify and characterize Na+ -activated K+ current (I(K(Na))) in guinea pig gastric myocytes under whole-cell patch clamp. After whole-cell configuration was established under 110 mM intracellular Na+ concentration ([Na+]i) at holding potential of -60 mV, a large inward current was produced by external 60 mM K+([K+] degree). This inward current was not affected by removal of external Ca2+. K+ channel blockers had little effects on the current (p>0.05). Only TEA (5 mM) inhibited steady-state current to 68+/-2.7% of the control (p<0.05). In the presence of K+ channel blocker cocktail (mixture of Ba2+, glibenclamide, 4-AP, apamin, quinidine and TEA), a large inward current was activated. However, the amplitude of the steadystate current produced under [K+]degree (140 mM) was significantly smaller when Na+ in pipette solution was replaced with K+ - and Li+ in the presence of K+ channel blocker cocktail than under 110 mM [Na+]i. In the presence of K+ channel blocker cocktail under low Cl- pipette solution, this current was still activated and seemed K+ -selective, since reversal potentials (E(rev)) of various concentrations of [K+]degree-induced current in current/voltage (I/V) relationship were nearly identical to expected values. R-56865 (10-20 microgram), a blocker of IK(Na), completely and reversibly inhibited this current. The characteristics of the current coincide with those of IK(Na) of other cells. Our results indicate the presence of IK(Na) in guinea pig gastric myocytes.


Subject(s)
Male , Female , Animals , Tetraethylammonium Compounds/pharmacology , Stomach/physiology , Sodium/metabolism , Potassium Channels/physiology , Potassium Channel Blockers/pharmacology , Myocytes, Smooth Muscle/physiology , Membrane Potentials , Guinea Pigs , Chlorides/pharmacology , Calcium/metabolism
6.
Article in English | IMSEAR | ID: sea-18777

ABSTRACT

BACKGROUND & OBJECTIVE: The occupational and non-occupational exposure to hexavalent chromium Cr (VI) is common. The effect of chromium compromises the immune response of the host. Dengue virus (DV) infection causes various changes in the peripheral blood cells. It is, therefore, possible that the chromium toxicity may affect the disease process during DV infection. The present study aims to study the effects of dengue virus infection on peripheral blood cells of mice fed Cr (VI) with drinking water. METHODS: One group of mice was given ad libitum drinking water containing Cr (VI) and the other group used as the normal control mice was given plain water to drink. At the 3, 6 and 9 wk of Cr (VI) drinking, a set of mice from each group was inoculated intracerebrally (ic) with DV and studied at the 4th and 8th day post inoculation. RESULTS: It was observed that Cr (VI) drinking led to reduction in lymphocytes, haemoglobin and the haematocrit values while the granulocyte, monocyte and platelet counts were increased. On the other hand, most of the parameters were decreased following inoculation of normal mice with DV. In Cr (VI)-fed mice the effects of DV infection were minimal. The most significant finding of these experiments was that the reduction in platelet counts following inoculation with DV was markedly less in Cr (VI)-fed mice than that in DV-inoculated normal control mice. INTERPRETATION & CONCLUSION: Cr(VI) compounds have been declared as a potent occupational carcinogen. On the contrary, Cr(III) salts such as chromium polynicotinate, chromium chloride and chromium picolinate, are used as micronutrients and nutritional supplements, and have been shown to exhibit health benefits in animals and humans. Whether therapeutic doses of chromium (III) compounds may be able to prevent the DV-induced fall in platelet counts, needs to be investigated.


Subject(s)
Administration, Oral , Animals , Blood Cell Count , Blood Platelets/cytology , Carcinogens , Chlorides/pharmacology , Chromium/administration & dosage , Chromium Compounds/pharmacology , Dengue/drug therapy , Dengue Virus/metabolism , Erythrocytes/drug effects , Hematocrit , Humans , Leukocytes/drug effects , Lymphocytes/drug effects , Mice , Monocytes/drug effects , Neutrophils/drug effects , Nicotinic Acids/pharmacology , Organometallic Compounds/pharmacology , Picolinic Acids/pharmacology , Platelet Count , Time Factors , Water/metabolism
7.
Indian J Exp Biol ; 2005 Apr; 43(4): 324-9
Article in English | IMSEAR | ID: sea-59079

ABSTRACT

In the present investigation we have examined the hypothesis that calcium-dependent K+ channels (K(Ca)) are involved in the sodium nitroprusside (SNP)-induced vasodilatation of goat coronary artery. SNP (10(-9)-3 x 10(-6) M), added cumulatively, relaxed K+ (30 mM)-contracted coronary artery ring segments in a concentration-dependent manner with an EC50 of 1.32 x 10(-7) M (95% CL, 0.93-1.86 x 10(-7) M; n = 21). K(Ca) blocker, tetraethyl ammonium (1 mM) caused a rightward shift in the concentration-response curve of SNP with a corresponding increase in EC50 (1.62 x 10(-6) M; 95% CL, 0.44-6.02 x 10(-6) M, n = 4) of nitro vasodilator. Lowering of extra cellular Ca2+ in the physiological saline solution to 1/4 of normal selectively attenuated the vasorelaxant response of SNP, thereby causing an increase in its EC50 (2.4 x 10(-6) M; 95% CL, 1.23-4.68 x 10(-6) M, n = 4). Exposure of the tissues to high K+ (80 mM) solution, a protocol adopted to reduce the K+ gradient across the cell membrane, markedly inhibited the coronary artery relaxations induced by SNP (EC50, 2.54 x 10(-6) M; 95% CL, 1.31-4.91 x 10(-6) M, n = 4), when compared with tissues contracted with low K+ (30 mM) solution (EC50 7.9 x 10(-8); 95% CL, 4.4 x 10(-8)-1.44 x 10(-7) M, n = 6). The results suggested that a major component of SNP-induced relaxation of goat coronary artery was mediated by K(Ca) channels.


Subject(s)
Animals , Barium Compounds/pharmacology , Calcium/metabolism , Chlorides/pharmacology , Coronary Vessels/drug effects , Dose-Response Relationship, Drug , Goats , Methylene Blue/pharmacology , Nitric Oxide Donors/pharmacology , Nitroprusside/pharmacology , Potassium Channel Blockers/pharmacology , Potassium Channels, Calcium-Activated/metabolism , Potassium Chloride/pharmacology , Vasodilation/drug effects
8.
Indian J Exp Biol ; 2004 Sep; 42(9): 913-8
Article in English | IMSEAR | ID: sea-57259

ABSTRACT

Present study was conducted on prostaglandin F2alpha (PGF2alpha), oxytocin, (OT), potassium chloride (KCI) and barium chloride (BaCl2) pre-contracted perimetrial uterine strips of dioestrus and pregnant buffaloes to evaluate the tocolytic efficacy of selective beta2 adrenoceptor agonists-albuterol (salbutamol) and terbutaline. Cumulative concentration-response curves of both the beta2 adrenoceptor agonists were constructed and the mean effective concentration (EC50) values determined and compared statistically. Based on the comparative EC50 values in relaxing the pre-contracted uterine strips with different spasmogens, the rank order potency of albuterol was found to be--PGF2alpha > BaCl2 > OT > KCl on uterine strips from dioestrus animals, while OT> BaCl2> PGF2alpha >KCl on the uterine strips of pregnant buffaloes. The rank order potency of terbutaline on uterine strips from dioestrus stage animals was- BaCl2 > OT > KCl > PGF2alpha, while BaCl2 > PGF2alpha > KCl > OT on uterine tissues of pregnant animals. Thus, irrespective of the state of uterus, whether gravid or non-gravid, KCl-depolarized uterine tissues required comparatively higher concentrations of albuterol or terbutaline to produce tocolytic effect. High concentrations of K+ in biophase may have interfered with the beta2 adrenoceptor agonists-induced outward K+ current and hyperpolarization. From the results of present study, it was evident that selective beta2 adrenergic agonists had good tocolytic efficacy on the uterus of buffaloes. Further, indirectly the possibility of existence and activation of K(Ca) channels by selective beta2 adrenoceptor agonists in mediating tocolysis of buffalo myometrium can not be ruled out, however, detailed studies using specific K(Ca) channel blockers are required for characterizing the nature of such channels in buffalo uterus.


Subject(s)
Abortifacient Agents, Nonsteroidal/pharmacology , Adrenergic beta-Agonists/pharmacology , Albuterol/pharmacology , Animals , Barium Compounds/pharmacology , Buffaloes , Chlorides/pharmacology , Dinoprost/pharmacology , Female , Oxytocin/pharmacology , Potassium Chloride/pharmacology , Pregnancy , Receptors, Adrenergic, beta-2/antagonists & inhibitors , Terbutaline/pharmacology , Tocolytic Agents/pharmacology , Uterine Contraction/drug effects , Uterus/drug effects
9.
Indian J Exp Biol ; 2004 Feb; 42(2): 149-51
Article in English | IMSEAR | ID: sea-57523

ABSTRACT

The effects of MnCl2 on vascular smooth muscle contraction induced by noradrenaline (NA) and KCl were investigated. Rings segments from rat aorta were isolated and changes in isometric tension recorded. MnCl2 (10 microM and 1 mM) significantly attenuated the contractile responses to NA and KCI. There were also reductions in the contractile responses to CaCl2 in NA- and KCl-stimulated rings, after pretreatment with MnCl2. The magnitude of the phasic contraction to NA was significantly reduced in presence of MnCl2. The results suggest that MnCl2 inhibits vascular smooth muscle contraction by influencing a Ca2+-mediated mechanism.


Subject(s)
Animals , Aorta, Thoracic/drug effects , Calcium/metabolism , Chlorides/pharmacology , Manganese Compounds/pharmacology , Muscle Contraction/drug effects , Muscle, Smooth, Vascular/drug effects , Norepinephrine/pharmacology , Potassium Chloride/pharmacology , Rats , Rats, Sprague-Dawley , Vasoconstrictor Agents/pharmacology
10.
Article in English | IMSEAR | ID: sea-112305

ABSTRACT

The antifungal effects of zinc chloride (znCl), Calcium chloride (CaCl), magnesium chloride (MgCl) as well as soot collected from a local kitchens were tested on five isolated species of the dermatophytes from cases of human dermatophytoses. Of these three metallic salts, ZnCl showed the highest inhibitory effect on the dermatophytes. At a concentration of 0.01 M it showed 100% inhibition on these fungi. Although the other two metallic salts showed some inhibitory effect CaCl at concentration between 0.01 M and 1 M showed only 50% inhibitory effect while MgCl at concentration between 0.1 M and 1 M showed less than 50% inhibitory effect on the fungi. Also soot inhibited the growth of all the dermatophytes tested at concentration between 0.1 and 2%. Trichophyton rubrum and Microspum audouinii appeared to be most sensitive to these compounds compared to the other three species which include T. mentagrophytes, T. tonsurans and M. gypseum.


Subject(s)
Arthrodermataceae/drug effects , Calcium Chloride/pharmacology , Carbon/pharmacology , Chlorides/pharmacology , Dose-Response Relationship, Drug , Humans , Magnesium Chloride/pharmacology , Zinc Compounds/pharmacology
11.
Arch. med. res ; 30(2): 82-8, mar.-abr. 1999. ilus, tab, graf
Article in English | LILACS | ID: lil-256628

ABSTRACT

Background. Cysteine-proteinases are thought to play an important role in E. histolytica pathogenicity. Although effective blockage of proteolytic activities can be obtained with sereveral known inhibitors, the high cellular toxicity of most of the inhibitors precludes experimentation with live cells or animal models. Specific cysteine-proteinase inhibitors that could be utilized in studies of virulence are of great need in the field of amebiasis. Methods. Cysteine-proteinase activities were determined in trophozoit lysates by azocasein degradation and after PAGE and gelatin zymograms. Inhibition of the activities was assessed in the presence of 0.01-2.5 mM concentrations of fivalent cations of the IIB and VIII series such as Zn, Cd, Hg, Ni, and Co. Reversibility was induced with 25 mM L-cysteine or 50 mM L-histidine and by metal chelation with 5 mM phenantroline. The inhibitory effect of ZnCI2 was tested with live cells in fibronectin-biding and cytotoxicity assays. Results. ZnCI2 specifically inhibited cysteine-proteinase activities in trophozoite lysates in a concentration-dependent manner. Additionally, 1.0-2.5 mM ZnCI2 bloked proteolysis in more than 70 percent. This inhibition was completely reverted by L-cysteine, L-histidine, or phenantroline. Similar results were obtained by analyzing indivual cysteine-proteinase activities separated in gelatin zymograms. At these concentrations, ZnCI2 significanty interfered with trophozoit adhesion, thus making amebas deficient in substrate degradation and cell damage. Conclusions. ZnCI2 is effective inhibitor of amebic cysteine-proteinases. Its low toxicity at relative high concentrations, high solubility, and low cost make it adequate for live cell experimentation and animal models of amebic virulence


Subject(s)
Animals , Cell Adhesion , Chlorides/pharmacology , Cysteine Proteinase Inhibitors/pharmacology , Cysteine Endopeptidases/metabolism , Entamoeba histolytica/enzymology , Zinc Compounds/pharmacology , Cell Adhesion/drug effects , Electrophoresis, Polyacrylamide Gel
12.
Indian J Exp Biol ; 1998 Jan; 36(1): 43-5
Article in English | IMSEAR | ID: sea-62938

ABSTRACT

Effect of chloride and diamide on testicular and epididymal angiotensin converting enzyme (ACE) activity was investigated using Hip-His-Leu as substrate in sheep. The chloride ions functioned as ACE activators, however, there was no linear correlation between the two. The optimum chloride concentrations were 500 mM for epididymal ACE and 900-1100 mM for testicular ACE. Further, optimum chloride concentration increased ACE activity of testis and epididymis 25.40- folds and 12.84- folds respectively of the activities at physiological chloride concentration. The differences found in the effect of chloride on testicular and epididymal ACE activity suggest dissimilar three dimensional structure of ACE in these tissues. Increased testicular and epididymal ACE activity on diamide pretreatment indicates that tissue oxidation may affect ACE activity.


Subject(s)
Angiotensin-Converting Enzyme Inhibitors/metabolism , Animals , Chlorides/pharmacology , Diamide/pharmacology , Epididymis/drug effects , Male , Peptidyl-Dipeptidase A/metabolism , Sheep , Sulfhydryl Reagents/pharmacology , Testis/drug effects
13.
Indian J Exp Biol ; 1993 Mar; 31(3): 235-7
Article in English | IMSEAR | ID: sea-58072

ABSTRACT

The psychoactive drugs imipramine, chlorpromazine and lithium chloride inhibit tryptamine tetrazolium reductase activity in vitro by 68, 60 and 33% respectively at a concentration of 1 x 10(-3) M while amphetamine negligibly inhibits the enzyme activity. No change in enzyme activity is observed in vivo.


Subject(s)
Animals , Brain/drug effects , Chlorides/pharmacology , Chlorpromazine/pharmacology , Dextroamphetamine/pharmacology , Imipramine/pharmacology , Lithium/pharmacology , Lithium Chloride , Male , Oxidoreductases Acting on CH-NH Group Donors/antagonists & inhibitors , Psychotropic Drugs/pharmacology , Rats
14.
Indian J Exp Biol ; 1992 Aug; 30(8): 736-7
Article in English | IMSEAR | ID: sea-59563

ABSTRACT

Effect of some pollutants like heavy metals, non-metals and pesticides on the circulating level of C-reactive protein (CRP) which is an acute phase plasma protein was studied in a freshwater murrel C. punctatus. Fish was exposed to nonlethal doses of these xenobiotics which were apparently safe. But the level of CRP detected by sensitive single radial immunodiffusion (SRID) technique showed that within 12 hr of exposure the nonlethal doses of xenobiotics could initiate the acute phase response in terms of elevated CRP titre. Heavy metals caused the acute phase within 24 hr, nonmetals and Metacid-50 within 48 hr exposure. The carbamate compound, carbaryl demonstrated a biphasic response to CRP level which may be correlated with the reversible type of anticholinesterase property of this compound while Metacid-50 is an irreversible type of anticholinesterase agent. The assessment of the CRP level in the serum of fish may be utilized as a primary bioindicator of a contaminated environment toxic enough to mount an acute phase response.


Subject(s)
Ammonia/pharmacology , Animals , C-Reactive Protein/biosynthesis , Cadmium/pharmacology , Cadmium Chloride , Carbaryl/pharmacology , Chlorides/pharmacology , Fishes/blood , Mercuric Chloride/pharmacology , Methyl Parathion/pharmacology , Phenols/pharmacology , Water Pollution, Chemical
15.
Indian J Exp Biol ; 1991 Jul; 29(7): 693-4
Article in English | IMSEAR | ID: sea-58687

ABSTRACT

Compared to non-metal toxicants (ammonia, 1.56 ppm; and phenol, 10 ppm), the metals (CdCl2, 30 ppm; HgCl2, 16.7 ppb; and ZnCl2, 6 ppm) significantly induced hepatic metallothionein (MT) concentrations in C. punctatus, exposed independently to non-lethal doses of these toxicants for 28 days. It is suggested that hepatic MT serves as a metal-sequestering protein and is involved in the detoxication of metals only and ensures protection from toxic chemicals in ambience.


Subject(s)
Animals , Chlorides/pharmacology , Fishes/metabolism , Gene Expression Regulation/drug effects , Hydroxides/pharmacology , Liver/metabolism , Mercuric Chloride/pharmacology , Metallothionein/biosynthesis , Phenol , Phenols/pharmacology , Stimulation, Chemical , Zinc/pharmacology , Zinc Compounds
16.
Indian J Physiol Pharmacol ; 1990 Oct; 34(4): 263-6
Article in English | IMSEAR | ID: sea-108276

ABSTRACT

Changes in the adrenal weight, adrenal 5-ene-3 beta-hydroxysteroid dehydrogenase (5-ene-3 beta-HSD) activity and serum levels of corticosterone were observed in male wistar rats after the treatment of lithium chloride in the doses of 100, 200 and 400 micrograms/100 g of body weight/day for 7, 14 and 21 days. The experiments indicate that 200 and 400 micrograms/100 g.b.w. administered for 14 and 21 days caused a significant stimulation in the activities of adrenal 5-ene-3 beta-HSD along with elevation of adrenal weights and serum levels of corticosterone. 100 micrograms of lithium chloride was not able to modulate the adrenal activity. Moreover, plasma levels of lithium remain in therapeutic range in this experiment at the doses of 200 and 400 micrograms/100 g body weight. Therefore, our data suggest that lithium can alter the adrenal activity within its therapeutic range according to the duration of treatment.


Subject(s)
3-Hydroxysteroid Dehydrogenases/metabolism , Adrenal Cortex/drug effects , Animals , Chlorides/pharmacology , Corticosterone , Dose-Response Relationship, Drug , Lithium/blood , Lithium Chloride , Male , Organ Size/drug effects , Rats , Rats, Inbred Strains , Time Factors
17.
Indian J Exp Biol ; 1990 Sep; 28(9): 801-5
Article in English | IMSEAR | ID: sea-61649

ABSTRACT

Activities of delta 5-3 beta- and 17 beta-hydroxysteroid dehydrogenase (delta 5-3 beta-HSD and 17 beta-HSD), Leydig cell nuclear area (LCNA) and spermatogenesis in the testis were observed after injection of lithium chloride in the 'antiserum to luteinizing hormone (LH)' treated toad. A significant decrease in the activities of steroidogenic enzymes, LCNA and spermatogenesis were noticed after the injections of 'antiserum to LH' to toads. Further decrease in the activities of the above parameters was observed in the lithium chloride--'antiserum to LH' treated toad. It is suggested that lithium chloride may inhibits testicular function without modulating the pituitary activity.


Subject(s)
17-Hydroxysteroid Dehydrogenases/metabolism , 3-Hydroxysteroid Dehydrogenases/metabolism , Animals , Bufonidae , Chlorides/pharmacology , Immune Sera , Lithium/pharmacology , Lithium Chloride , Luteinizing Hormone/immunology , Male , Spermatogenesis/drug effects , Testis/drug effects
18.
Indian J Biochem Biophys ; 1989 Oct; 26(5): 301-4
Article in English | IMSEAR | ID: sea-28036

ABSTRACT

Denaturation of ribonuclease-A by lithium chloride has been studied using difference spectral, circular dichroic and viscometric measurements. The difference spectral results were interpreted in the light of our observations that the solvent effect of the denaturant on the tyrosyl residue is non-linear. It has been observed that (1) the lithium chloride-denatured protein contains 3% alpha-helix and 18% beta-structure, and (2) only two of the three buried tyrosyl residues are normalized in the denatured protein.


Subject(s)
Chlorides/pharmacology , Circular Dichroism , Lithium/pharmacology , Lithium Chloride , Protein Denaturation/drug effects , Ribonuclease, Pancreatic , Spectrum Analysis , Viscosity
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