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Biomedical subjects

M V Reddy

Publications and source records attributed to M V Reddy.

At least 109 records · Page 6Linked to original sources
PubMed1983

Acid alpha naphthyl acetate esterase positive lymphocytes in cattle with carcinoma of the mucosa of the ethmoid.

The T lymphocytes (alpha naphthyl acetate esterase positive cells) were estimated in the peripheral blood smears as well as in the separated lymphocytes in tumour bearing and non-tumour bearing control cattle. The results obtained with both techniques were similar and it was suggested that the blood smear staining technique could be routinely used in place of the time consuming and laborious cell separation technique. The T lymphocyte percentage in the peripheral blood of the tumour bearing animals was lower than that of healthy control animals. However, the animals in stages 1 and 2 showed slightly higher values than the stage 3 tumour bearing cattle.

Adenocarcinoma↗
PubMed1982

Evaluation of the cell mediated immune response in pigs using 2,4-dinitrochlorobenzene.

An experiment was carried out to measure the cell mediated immune response in pigs by sensitising the animals with 2,4-dinitrochlorobenzene (DNCB). The pigs could be sensitised with one application of DNCB. The appropriate site for application and the sensitising and challenge dose were standardised. The histological response was characteristic of a delayed hypersensitivity reaction.

Animals↗
PubMed1982

32P-postlabeling analysis of non-radioactive aromatic carcinogen--DNA adducts.

A newly developed enzymatic 32P-postlabeling method was applied to the analysis of DNA's containing non-radioactive arylamine, arylamide, and polycyclic aromatic hydrocarbon adducts. DNA reacted in vitro with N-hydroxy-2-amino-fluorene, N-acetoxy-2-acetylaminofluorene, and 7 beta,8 alpha-dihydroxy-9 alpha,10 alpha-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene, respectively, as well as DNA preparations from the liver of rats treated with N-hydroxy-2-acetylaminofluorene and benzo[a]pyrene, respectively, were enzymatically digested to deoxyribonucleoside 3'-monophosphates, which were then converted to [5'-32P]deoxyribonucleoside 3',5'-bisphosphates by T4 polynucleotide kinase-catalyzed [32P]phosphate transfer from [gamma-32P]ATP. The 32P-labeled nucleotides were resolved by anion-exchange t.l.c. on polyethyleneimine-cellulose and detected by autoradiography. Aromatic adduct nucleotides were found to be retained at the origin in aqueous electrolyte solutions, but to migrate as distinct spots in solvents containing 7-8.5 M urea. Advantage was taken of this observation to remove 32P-labeled normal DNA nucleotides from adduct nucleotides. This purification enabled the detection of a single adduct in 10(7)-10(8) normal nucleotides. The method appears applicable to the ultrasensitive detection of a large number of carcinogen--DNA adducts of diverse structure without requiring radioactive carcinogens or specific antibodies.

Animals↗
PubMed1981

Specificity of deoxycytidylate antibodies.

Antibodies to deoxycytidylate (dpC) were elicited in rabbits using a thyroglobulin (Tg) conjugate of dpC. The specificity of the antibodies was determined by measuring the inhibition of the binding of [3H]dpC to the antibodies by various non-radioactive nucleotides or derivatives. The antibodies were found to distinguish dpC from pC and DNA from RNA, probably due to their specificity for the conformation of the deoxycytidylate.

Animals↗
PubMed1981

32P-labeling test for DNA damage.

Covalent adducts formed by the reaction of DNA with chemical carcinogens and mutagens may be detected by a 32P-labeling test. DNA preparations exposed to chemicals known to bind covalently to DNA [N-methyl-N-nitrosourea, dimethyl sulfate, formaldehyde, beta-propiolactone, propylene oxide, streptozotocin, nitrogen mustard, and 1,3-bis(2-chloroethyl)-1-nitrosourea] were digested to a mixture of deoxynucleoside 3'-monophosphates by incubation with micrococcal endonuclease (EC 3.1.31.1) and spleen exonuclease (EC 3.1.16.1). The digests were treated with [gamma-32P]ATP and T4 polynucleotide kinase (ATP:5'-dephosphopolynucleotide 5'-phosphotransferase, EC 2.7.1.78) to convert the monophosphates to 5'-32P-labeled deoxynucleoside 3',5'-bis-phosphates. These compounds were then separated on polyethyleneimine-cellulose thin layers in ammonium formate and ammonium sulfate solutions. Autoradiograms of the chromatograms obtained by this high-resolution procedure showed the presence of nucleotides derived from chemically altered, as well as normal, DNA constituents. Maps from DNA exposed to any of the chemicals used exhibited a spot pattern typical for the particular chemical. This method detected a single adduct in 10(5) DNA nucleotides without requiring that the compound under investigation be radioactive and thus provides a useful test to screen chemicals for their capacity to damage DNA by covalent binding.

Animals↗
PubMed1981

Urinary glycoconjugates in schizophrenic patients.

The level of glycoconjugates excreted in the urine of five schizophrenic patients was compared to that excreted by six controls. Urinary samples were fractionated by means of gel filtration and anion exchange chromatography to yield (i) fraction I consisting of basic, neutral, or slightly acidic glycopeptides and/or oligosaccharides, (ii) fraction II consisting of acidic glycopeptides and/or oligosaccharides, and (iii) fraction III consisting of glycosaminoglycans (acidic mucopolysaccharides). The hexose levels of fraction II (p less than 0.05) and uronate levels of fraction III (p less than 0.025) were significantly reduced in schizophrenic patients. The ratio of galactose/mannose in the glycoconjugates of fraction II was lower than normal in the urine from schizophrenic patients. Significantly (p less than 0.05) lower levels of rhamnose and higher levels of fucose were found in the glycoconjugates of fraction I from schizophrenic patients. Contrary to a previous report, we found no evidence for the presence of an abnormally elevated rhamnose-containing glycoprotein or glycoconjugate in fraction II. I appears that the pattern of metabolism of glycoproteins and glycosaminoglycans in schizophrenic patients deviates from the normal.

Adult↗