Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 47
Filter
Add more filters










Publication year range
1.
Indian J Exp Biol ; 36(3): 273-82, 1998 Mar.
Article in English | MEDLINE | ID: mdl-9754060

ABSTRACT

The effects of sub-chronic doses of malathion exposure on humoral and cell-mediated immune (CMI) responses were studied in male albino mice, rats and rabbits using sheep red blood cells (SRBC), tetanus toxoid and ovalbumin as antigens. The humoral immune response was assessed by estimating serum immunoglobulin (IgM and IgG) concentrations, antibody titre against antigens and splenic-plaque forming cells (PFC). The CMI response was studied by using the leucocyte migration inhibition (LMI) and macrophage migration inhibition (MMI) tests. In general there were (a) attenuation in antigen induced antibody response, (b) suppression of PFC, and (c) marked inhibition of LMI and MMI factors. Sub-chronic malathion exposure induced differential degrees of humoral and CMI suppression in these experimental animals. However, both cellular and humoral immune responses were decreased in a dose-time dependent pattern and a consistent trend was observed. The threshold level of the malathion for inducing immune suppression depends on the animal species, type of antigen used, and the method of immunological assay. In view of the widespread use of malathion a comparative assessment of immune responses using different experimental animals and antigens is an important aspect of its safety evaluation.


Subject(s)
Antibody Formation/drug effects , Immunity, Cellular/drug effects , Insecticides/toxicity , Malathion/toxicity , Animals , Male , Mice , Rabbits , Rats
3.
J Commun Dis ; 21(1): 34-8, 1989 Mar.
Article in English | MEDLINE | ID: mdl-2509545

ABSTRACT

An extra band of isoenzyme lactate dehydrogenase (LDH) was obtained in case of Plasmodium knowlesi free parasite as compared to normal monkey blood. This extra band could be resolved due to the decreasing amount of substrate concentration. Agarose electrophoresis technique was used to separate the isoenzyme bands.


Subject(s)
L-Lactate Dehydrogenase/analysis , Plasmodium/enzymology , Animals , Electrophoresis, Agar Gel , Haplorhini , Isoenzymes
7.
Arch Toxicol ; 59(4): 279-84, 1986 Dec.
Article in English | MEDLINE | ID: mdl-3827596

ABSTRACT

The present study was designed to evaluate the effect of sub-chronic doses of endosulfan on humoral and cell-mediated immune (CMI) responses in albino rats. Male albino rats were given a diet containing 5, 10 or 20 ppm endosulfan for 8-22 weeks and immunized with tetanus toxoid in Freund's complete adjuvant subcutaneously 20 days before terminating the exposure. The humoral immune response was studied by serum globulin level, immunoglobulin (IgM and IgG) concentration and antibody titre against tetanus toxoid. The CMI response was studied by leucocyte migration inhibition (LMI) and macrophage migration inhibition (MMI) factors. The antigen-induced increases in serum globulin fraction and immunoglobulin level were reduced at high doses of the endosulfan after 12 weeks of exposure. Antibody titre was significantly decreased in endosulfan-exposed rats at 10 and 20 ppm levels and a consistent trend was observed. Rats in the 10 and 20 ppm dose groups had significantly depressed LMI and MMI responses. Results obtained in this study revealed marked suppression of the humoral and CMI responses in rats administered with sub-chronic doses of endosulfan. Both cellular and humoral immune responses were decreased in a dose-time dependent pattern. Suppression of immune responses by endosulfan is clearly an important aspect of its toxicology.


Subject(s)
Antibody Formation/drug effects , Endosulfan/pharmacology , Immunity, Cellular/drug effects , Animals , Cell Migration Inhibition , Endosulfan/administration & dosage , Immunoglobulins/drug effects , In Vitro Techniques , Leukocytes/drug effects , Macrophages/drug effects , Male , Rats , Rats, Inbred Strains , Serum Albumin/drug effects , Serum Globulins/drug effects , Tetanus Toxoid/immunology , Time Factors
10.
Folia Parasitol (Praha) ; 33(2): 107-13, 1986.
Article in English | MEDLINE | ID: mdl-3522381

ABSTRACT

Kupffer cells from the liver and erythrocytes from peripheral blood were collected at the post-patent period from albino rats infected earlier with Plasmodium berghei and rhesus monkeys infected earlier with P. cynomolgi var. bastianelli or P. knowlesi. The cells were subinoculated into individual normal recipients. These recipients subsequently showed parasitaemia in their circulation. The parasites present in Kupffer cell preparations were found to be sensitive to trypsin treatment, while those in erythrocytes were found to be resistant to trypsin treatment. This differential sensitivity of parasites to trypsin was observed in all the three species of plasmodia studied so far.


Subject(s)
Erythrocytes/parasitology , Kupffer Cells/parasitology , Malaria/parasitology , Plasmodium/drug effects , Trypsin/pharmacology , Animals , Macaca mulatta , Male , Plasmodium berghei/drug effects , Rats , Rats, Inbred Strains
11.
Br J Nutr ; 54(3): 563-6, 1985 Nov.
Article in English | MEDLINE | ID: mdl-2446655

ABSTRACT

1. Albino rats were fed on diets containing 30, 120 or 200 g protein/kg with or without the incorporation of dichlorodiphenyltrichloroethane (DDT) or hexachlorocyclohexane (HCH) at 100 mg/kg diet for 4 weeks. 2. The activities of the liver microsomal enzymes NADPH-cytochrome reductase (EC 1.6.2.4), flavoprotein-linked monooxygenase (EC 1.14.14.1) and O-demethylase were significantly greater in animals fed on 120 and 200 g protein/kg diet compared with those fed on 30 g protein/kg diet. 3. The inclusion of DDT or HCH at all protein intakes led to further significant rises in microsomal enzyme activities but the increases were much greater for animals receiving the 120 and 200 g protein/kg diets than for those receiving the 30 g protein/kg diet. 4. The results imply that detoxification of DDT or HCH was carried out more effectively at the higher protein intakes.


Subject(s)
DDT/pharmacology , Dietary Proteins/pharmacology , Hexachlorocyclohexane/pharmacology , Microsomes, Liver/enzymology , Animals , DDT/pharmacokinetics , Dietary Proteins/administration & dosage , Hexachlorocyclohexane/pharmacokinetics , Inactivation, Metabolic/drug effects , Male , Microsomes, Liver/drug effects , NADPH-Ferrihemoprotein Reductase/metabolism , Oxidoreductases, O-Demethylating/metabolism , Oxygenases/metabolism , Rats
SELECTION OF CITATIONS
SEARCH DETAIL
...