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Biomedical subjects

H N Singh

Publications and source records attributed to H N Singh.

At least 19 recordsLinked to original sources
PubMed2006

Distribution patterns of natural radioactivity and delineation of anomalous radioactive zones using in situ radiation observations in Southern Tamil Nadu, India.

In situ radiation measurements in the beach sectors and adjacent hinterlands and along rivers in the interiors of southern peninsular India were carried out using a portable radiation survey meter. A very high intrinsic anomalous radioactivity >26microGy/h has been observed in the hinterlands within a fresh quarry and weathered boulders in the syenite rock body around Puttetti in the western Kanyakumari district of southern Tamil Nadu. Over the weathered hillocks in the hinterlands adjacent to the coast around Inayam, Kurumpanai and Midalam, the in situ radiation measurements have also exhibited high radioactivity ranging from 4 to 22microGy/h which is significantly higher than the radiation exposure rates (RER) observed along the beach sectors at various locations from Chavara to Tuticorin (1-14microGy/h). The observed radiation levels are presumably the highest concentration in southern India and it is the first time that such a high intrinsic radiogenic source in the hinterlands is reported in southwest coast of India. It is also observed based on the laboratory analysis of samples and in situ radiation data that the rivers/channels in this region contain insignificant level of radioactivity concentration and hence they do not contribute much to the placer deposits on the beaches. The placer deposits associated with significant RER (both in situ observations as well as laboratory estimates from samples) in the beach sectors from Kadiapattanam to Inayam are inferred to be derived through the country rocks/weathered hillocks in the immediate hinterlands.

Geography↗
PubMed2005

Analysis of normal electrocardiograms of Jamunapari goats.

In the present study, the normal electrocardiographic (ECG) values in the adult male Jamunapari breed of the goats were described. The mean heart rate in the goats was 127 +/- 3.46 per minute and ranged 107 and 168. The amplitudes and duration of various waveforms of ECG for six standard limb leads (I, II, III, aVL, aVR and aVF) were estimated. The overall P, QRS and T amplitudes (millivolts) were 0.065 +/- 0.01, 0.47 +/- 0.06 and 0.20 +/- 0.014 respectively. The duration (seconds) of these wave forms were 0.042 +/- 0.005, 0.033 +/- 0.002 and 0.10 +/- 0.014, respectively. The P-R interval and R-R intervals ranged between 0.06- 0.14 and 0.40-0.58 respectively. The average Q-T interval was 0.24 +/- 0.01 second, indicating the time for which the caprine ventricle remained depolarized. The corrected QT interval was also calculated which was found to vary from 0.24 to 0.57. The mean frontal plane vectors for the wave forms P, QRS and T wave forms were +49.99 +/- 6.02, +37.34 +/- 4.05 and +52.26 +/- 6.79 degrees respectively.

Animals↗
PubMed2000

Aspiration vs nonaspiration technique of cytodiagnosis--a critical evaluation in 160 cases.

The two sampling techniques were studied in 160 randomly selected cases of superficial swellings in various sites of the body. They were sampled by fine needle aspiration (FNA) and by non-aspiration (NA) (a needle without application of aspiration pressure). Cell samples were cytologically assessed and critically evaluated using five objective parameters. Contamination with blood was more in lymphnode, thyroid and liver lesions in aspiration smears than NA smears and values were statistically significant. Similarly when compared for the degree of cellular trauma and cellular degeneration statistically significant better results were obtained by nonaspiration technique for lymphnode lesions. Regarding amount of cellular material obtained by FNA, statistical significant better results were found for breast lesions only. Statistically significant better maintenance of architecture was observed only for thyroid lesions by NA technique. Better average scores were observed by NA technique for lymphnode and thyroid only. Categorizing all the smears obtained by FNA & NA on the basis of their scores according to predetermined criteria, greater number of diagnostically adequate specimens were obtained by FNA than by NA but the number of diagnostically superior specimens obtained by NA technique was found to be more than that by FNA. The difference was found to be statistically significant. However the number of inadequate smears was also more by NA technique than by FNA technique.

Biopsy, Needle↗
PubMed1994

Common nitrogen control of caesium uptake, caesium toxicity and ammonium (methylammonium) uptake in the cyanobacterium Nostoc muscorum.

Studies were carried out to examine the role of ammonium transport activity in the control of caesium uptake and toxicity in Nostoc muscorum. The results showed a definite specific role of the ammonium-repressible/derepressible ammonium transport system of the cyanobacterium in caesium uptake, accumulation and toxicity. Furthermore, the results showed that N. muscorum can acquire resistance against diazotrophically-associated caesium toxicity when supplied with ammonium as a nitrogen source. In addition, alternatively, a mutant strain was Cs-resistant in the absence of any effect on NH(+4)-transport, suggesting that Cs+ resistance may be determined at more than one cellular site.

Biological Transport↗
PubMed1994

Mutational analysis of the NH4+-nitrogen controls that regulate ammonium transport activity, heterocyst differentiation, nitrogenase activity and the heterocyst-spacing pattern in the cyanobacterium Nostoc muscorum.

Mutational analysis of the genetic determinants mediating NH(4+)-nitrogen regulating effects on NH(4+)-transport activity, heterocyst differentiation, nitrogenase activity and heterocyst pattern formation was carried out in Nostoc muscorum. Evidence suggested the operation of three separate genetic determinants in such nitrogen control; one mediating NH(4+)-repression control on both heterocyst formation and NH(4+)-transport activity, a second (Nif-R) mediating NH(4+)-repression control on nitrogenase synthesis/activity and a third (Pat-R) essential for intercalary heterocyst formation/distribution. Ammonia itself functioned as repressor signal of heterocyst formation and nitrogenase synthesis/activity and the glutamine synthetase enzyme played no role in the repression/derepression control of heterocyst development and functional nitrogenase formation.

Bacterial Proteins↗
PubMed1993

Mutational replacement of molybdenum by vanadium in assimilation of N2 or NO3- as nitrogen source in the cyanobacterium Nostoc muscorum.

Tungsten resistant (Wr) mutants of Het+Nif+Nia+, Het+Nif-Nia+ and Het+Nif+Nia- strains of Nostoc muscorum were isolated with severely defective molybdate transport activity. All such mutants showed vanadium (V)-dependent nitrogenase activity and/or nitrate reductase activity and V-dependent growth on N2-nitrogen and/or NO3(-)-nitrogen and V-dependent NO3(-)-repression of heterocyst formation and nitrogenase activity. None of them grew with molybdenum (Mo) under parallel growth condition. Results strongly suggest the ability of V to replace Mo in N2-assimilation or NO3(-)-assimilation under Mo-deficiency.

Biological Transport↗
PubMed1992

Dopaminergic regulation of luteinizing hormone-releasing hormone release at the median eminence level: immunocytochemical and physiological evidence in hens.

Theoretically, the most effective inhibitory control of hypophysiotropic luteinizing hormone-releasing hormone (LHRH) release might occur through a presynaptic inhibition of LHRH neuronal terminals at the median eminence (ME) level. Since: (a) we have recently reported the existence of synaptic contacts between dopamine- and LHRH-containing processes in the ewe ME, and (b) nutritional deprivation induces an ovulatory failure in both birds and mammals, we have assessed the possibility that the anovulatory state induced by feed withdrawal (FW) in laying hens, might be caused by a dopaminergic inhibition of LHRH release at the ME level. Laying hens at the start (35 weeks old) and end (75 weeks old) of their commercial egg-laying life were killed at 0, 1, 2 and 4 days after FW. Serum luteinizing hormone (LH) and progesterone (P4), in vitro release of LHRH by isolated ME, and LHRH content in ME and preoptic area (POA) were determined by RIA. ME content of dopamine (DA) and its main metabolite 3,4-dihydroxyphenylacetic acid (DOPAC) were assessed by LCED. The distribution of LHRH and tyrosine hydroxylase (TH)-containing processes at the ME level of the hen was determined immunocytochemically. In the hen, LHRH-containing cell bodies are localized in the anterior hypothalamus and medial POA. LHRH-containing axons project toward the ME and infundibulum through the ventral-lateral hypothalamus. TH-containing perikarya are concentrated in the arcuate nucleus and in the adjacent part of the periventricular nucleus, dorsal to the arcuate. TH-containing axons converge toward the ME and descend into the infundibulum. Dense concentrations of TH- and LHRH-containing processes are located in the lateral and mediobasal portions of the external layer of the ME, providing opportunities for synaptic interactions between them. Ovulatory failure and regression of the ovary and reproductive tract occurred 2-3 days after FW at the end, but not at the beginning of the hen's commercial egg-laying life. After FW, hens at the end of their productive life had higher (p less than 0.01) tuberoinfundibular DA turnover, produced less LHRH, and had lower serum LH and P4 than hens undergoing FW at the beginning of their productive life. In addition, in vitro release of HRH from denervated ME tissue of hens undergoing FW at the end of their commercial egg-laying life was higher and was reversed in a dose-dependent fashion by DA, but not by serotonin. Thus, the ovulatory failure associated with FW in laying hens might be caused by a presynaptic inhibition of in vivo LHRH release at the level of ME hypothalamic neuronal terminals.

3,4-Dihydroxyphenylacetic Acid↗
PubMed1991

Evidence for energy-dependent copper efflux as a mechanism of Cu2+ resistance in the cyanobacterium Nostoc calcicola.

Wild-type Nostoc calcicola carried out oxygenic photosynthesis extremely sensitive to copper. A Cu(2+)-resistant mutant (Cu-R1) of the cyanobacterium grew normally at high concentrations of Cu2+. Its ability to grow under such conditions was found to be due to mutational acquisition of an energy-dependent efficient system of Cu(2+)-efflux, which rendered Cu(2+)-inhibited oxygenic photosynthesis fully reversible.

Biological Transport, Active↗
PubMed1991

Pharmacological modulation of rat monocytes: in vivo effects on Ia expression and interleukin-1 production.

We have shown that during the developing phase of adjuvant disease (AD) in rats the expression of MHC class II (Ia) antigens on blood monocytes (BM) was enhanced. The results of a study in established AD are reported now. Four agents were tested: indomethacin and diclofenac-sodium (1 mg/kg/day); levamisole and prinomide (10 mg/kg/day), administered orally from day 18-31 after induction of AD. We assessed the following BM parameters: Ia expression, interleukin-1 (sIL-1) production, and membrane bound IL-1 (mIL-1). In AD Ia expression was enhanced, no changes occurred in mIL-1 or sIL-1. Indomethacin treatment reduced sIL-1 production, levamisole Ia expression and mIL-1 activity, prinomide all three parameters measured and diclofenac, though clinically effective, none.

Animals↗
PubMed1991

Relationship of blood markers to disease severity and drug efficacy in rat adjuvant arthritis.

Rat adjuvant arthritis (AA) was used as a model to evaluate several blood markers as possible predictive indicators of drug efficacy. AA was induced in Sprague-Dawley rats by the injection of complete Freund's adjuvant into the right hind foot pad. The rats were dosed p.o. from day 18 to day 31 with levamisole (10 mg/kg), indomethacin (1 mg/kg), diclofenac sodium (0.5 & 1 mg/kg), and prinomide (10 & 20 mg/kg). Disease severity was assessed by paw circumference on day 31. The following blood markers were analyzed: hyaluronate by ELISA, prostaglandin E2 by RIA, ESR by micro-dispette, total PMN by Technicon H-1, and albumin by BCG dye. Blood marker correlation (r) to disease severity was: hyaluronate (0.71), prostaglandin E2 (0.58), ESR (0.52), PMN (0.58), and albumin (-0.71). The relative rank order of drug efficacy (indomethacin, diclofenac sodium, and prinomide) did not differ using the change in paw circumference (day 31-day 17) or blood markers. Levamisole exacerbated the disease as measured by all the above parameters. Thus, these blood markers provide additional information for the statistical evaluation of drugs in rat adjuvant arthritis.

Animals↗
PubMed1991

Influence of different forms of nitrogen on uptake of ammonium, glutamate and glutamine in the cyanobacterium Nostoc muscorum.

Effect of various types of nitrogen nutrition was studied on the uptake of ammonium, glutamate and glutamine by Nostoc muscorum and its Het-Nif- mutant. Ammonium nitrogen acted as a potent inhibitor/repressor of ammonium, glutamate and glutamine transport. Nitrate nitrogen was found to be a strong inhibitor/repressor of ammonium transport, a partial inhibitor/repressor of glutamate transport but, caused a partial stimulation of glutamine transport.

Ammonia↗
PubMed1991

Evidence for a role of glutamine synthetase in assimilation of amino acids as nitrogen source in the cyanobacterium Nostoc muscorum.

Methylammonium/ammonium ion, glutamine, glutamate, arginine and proline uptake, and their assimilation as nitrogen sources, was studied in Nostoc muscorum and its glutamine synthetase-deficient mutant. Glutamine served as nitrogen source independent of glutamine synthetase activity. Glutamate was not metabolised as a nitrogen source but still inhibited nitrogenase activity and diazotrophic growth. Glutamine synthetase activity was essential for the assimilation of N2, ammonia, arginine and proline as nitrogen sources but not for the control of their transport, heterocyst formation, and production of ammonia or aminoacid dependent repressor signal for N2-fixing heterocysts. These results also suggest that glutamine synthetase serves as the sole route of ammonia assimilation and glutamine synthesis, and ammonia per se as the repressor signal for N2-fixing heterocysts and methylammonium (ammonium) transport.

Amino Acids↗
PubMed1990

Genetic transformation of glutamine auxotrophy to prototrophy in the cyanobacterium Nostoc muscorum.

Glutamine auxotrophic (Gln-) and L-methionine D,L-sulfoximine (MSX) resistant (MSXr) mutants of N. muscorum were isolated and characterized for nitrogen nutrition, nitrogenase activity, glutamine synthetase (GS) activity and glutamine amide, alpha-keto-glutarate amido transferase (GOGAT) activity. The glutamine auxotroph was found to the GOGAT-containing GS-defective, incapable of growth with N2 or NH4+ but capable of growth with glutamine as nitrogen source, thus, suggesting GS to be the primary enzyme of both ammonia assimilation and glutamine formation in the cyanobacterium. The results of transformation and reversion studies suggests that glutamine auxotrophy is the result of a mutation in the gln A gene and that gln A gene can be transferred from one strain to another by transformation.

Ammonia↗