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Biomedical subjects

S N Pradhan

Publications and source records attributed to S N Pradhan.

At least 19 recordsLinked to original sources
PubMed1992

Glycaemic index of conventional carbohydrate meals.

The glycaemic index (GI) and the triacylglycerol response were measured in thirty non-insulin-dependent diabetes mellitus patients given 50 g portions of five different conventional Indian meals containing semolina (Triticum aestivum) cooked by two different methods, or combinations of semolina and pulse (black gram dhal (Phaseolus mungo), green gram dhal (Phaseolus aureus) or Bengal gram dhal (Cicer arietum)). There were no significant differences among meals in mean GI except for meals based on roasted semolina or semolina-black gram dhal. Compared with the blood glucose response for a 50 g glucose load, only meals based on steam-cooked semolina and semolina-Bengal gram dhal elicited a significantly lower response at 1 h postprandially, and only meals based on semolina-black gram dhal at 2 h postprandially. No significant differences were found among the meals in the triacylglycerol-response.

Blood Glucose↗
PubMed1991

Behavioral effects of ethanol inhalation in rats.

Behavioral effects of ethanol inhalation were studied on two fixed-ratio (FR) liquid-reinforced schedules and a continuous reinforcement (CRF) schedule intracranial self-stimulation (SS) in rats using the inhalational behavioral chamber designed in our laboratory. In the FR-24 schedule ethanol caused a decrease of reinforcement rate at 161 ppm and higher concentrations. In the FR-50 schedule decreases of the rate were observed at 102 ppm and 203 ppm. In the SS behavior ethanol produced a decrease in the rate of reinforcement at 603 ppm and higher concentrations. In rats of this schedule, blood ethanol concentrations were measured to be 393 micrograms/ml and 545 micrograms/ml after exposure to 600 ppm and 1200 ppm of ethanol respectively. Acute tolerance to ethanol was observed in these experiments, particularly in the FR-24 schedule. Thus ethanol inhalation could produce adequate blood concentrations so as to produce behavioral effects.

Administration, Inhalation↗
PubMed1991

Effects of ethanol inhalation on EEG in rats.

Effects of ethanol on duration of stages of sleep-wake cycle and EEG power spectra were measured during a 2-h exposure in a dynamic inhalational chamber in rats. Rats were exposed to one of four graded concentrations (approx. 100, 400, 800 and 1600 ppm) of ethanol on different days. Ethanol was found to increase the duration of waking (W) with a decrease in duration of rapid eye movement (REM) sleep at 100 and 400 ppm. No effect was observed at 800 and 1600 ppm on the stages of sleep-wake cycle or at 100-1600 ppm on EEG power spectra from the somatosensory or visual cortices. Results indicate that ethanol administered by inhalation could produce arousal action at low doses, but did not have any effect on EEG power spectrum at the concentrations used.

Administration, Inhalation↗
PubMed1990

Sensitivity of EEG in young rats to toluene exposure.

Effects of toluene on the electroencephalogram (EEG) and its power spectra were measured during a 2-hr exposure in a dynamic inhalational chamber in young rats (30-53 days old) and compared to those in adult rats (63-77 days old). Rats were exposed to one of the three concentrations [low (108-111 ppm), medium (160-163 ppm), and high (407-432 ppm)] of toluene on different days. In tests on sleep-wake cycle, in the young animals the duration of the wake stage (W) was increased with decreases of rapid eye movement (REM) and non-REM (NREM) sleep during hr 1 and hr 2 of exposure to the low concentration. These effects were marked at the medium and the high concentrations. In adult rats, at the low concentration the increase of W and the decrease of REM were observed only at hr 1; however, at medium and high concentrations these changes of W and REM sleep were marked along with a decrease of NREM. Comparison of the changes of duration of different states in rats of two age groups showed that there was a significant difference in the increase of W and the decrease of NREM sleep in young rats at hr 2 of exposure to low concentrations only compared to those in adult rats. Tested on power spectrum in young rats during REM sleep recorded from the visual cortex, the power of delta waves increased at the medium and high concentrations and that of theta wave decreased at the high concentration during hr 2 of exposure compared to the controls.(ABSTRACT TRUNCATED AT 250 WORDS)

Aging↗
PubMed1990

Glycemic index of traditional Indian carbohydrate foods.

The glycemic index (GI) was determined in 36 non-insulin-dependent diabetes mellitus patients who were fed 50 g carbohydrate portions of six Indian conventional foods, including rice, a combination of rice-legume (Bengalgram, peas, and greengram), and a combination of rice-dal (greengram dal and redgram dal -- dal is dehusked and split legume). In addition to the GI, triglyceride (TG) responses of these foods were also determined. A higher GI was obtained for rice and for rice with peas; all other combinations yielded lower glycemic indices. However, all the foods produced significantly lower blood glucose response 2 hours postprandially as compared with blood glucose responses to a 50 g glucose load for the same group. No significant difference was observed for TG responses to the different foods.

Blood Glucose↗
PubMed1989

Rebound increase of basal cAMP level in NG108-15 cells during chronic morphine treatment: effects of naloxone and chloramphenicol.

The effects of morphine on the basal cAMP level in the neuroblastoma X glioma NG108-15 hybrid cell line have been studied. Morphine (10 microM) added to the incubation media at hr 0 caused a rapid and significant decrease in the cAMP level up to hr 1; the level then slowly returned to the control at hr 6, and gradually increased to its peak at hr 36, returning to the control at hr 60. These results provide the first evidence for a delayed rebound increase of cAMP during morphine treatment. Naloxone (10 microM) added at hr 0 concomitantly with morphine blocked the morphine-induced decrease in cAMP level at hr 1 and attenuated its increase at hr 36. However, when naloxone was added at hr 5.5, the cAMP level significantly increased at hr 6, and at hr 36 the cAMP level increase was the same as in the case of morphine alone. Furthermore when naloxone was added 0.5 hr prior to harvesting the cells at hr 6, 12, 24 and 36, the cAMP level showed an immediate increase at each time point up to about the same level as observed with morphine alone at hr 36. Chloramphenicol, a protein synthesis inhibitor (100 microM) itself caused little or no change in the cAMP level. Added 30 min before morphine, chloramphenicol decreased the morphine-induced rebound increase at hr 36 in a concentration-dependent manner without any significant effect on cAMP decrease at hr 1. However when chloramphenicol was added at hr 5.5, the morphine-induced rebound increase at hr 36 was also attenuated, thereby suggesting an involvement of macromolecular synthesis in the rebound increase of cAMP which may be used as a model for the development of morphine dependence.

Chloramphenicol↗
PubMed1989

Effects of toluene exposure on the spontaneous cortical activity in rats.

Effects of toluene on the electroencephalogram (EEG) and its power spectra were measured during a 2-hr exposure in a dynamic inhalational chamber in rats. Rats were exposed to one of six graded concentrations (110.6, 162.5, 432, 676, 1558, 2730 ppm) of toluene on different days. It was found that the duration of waking (W) was increased with a decrease in duration of rapid eye movement (REM) sleep even at 110.6 ppm. Duration of nonrapid eye movement (NREM) sleep was decreased with an increase of W and a decrease of REM sleep at 162.5 ppm. Dose-related effects were noted in higher concentrations. The power of delta frequency band was increased with a decrease of theta frequency band power at hr 1 of exposure to 676 ppm during REM sleep recorded from the visual cortex. The power of theta frequency band was also decreased at hr 2 of exposure at 432 ppm. During W and NREM sleep power spectra were not changed significantly. Results indicate that the changes of EEG are a sensitive measure of the effects of toluene on the central nervous system (CNS).

Administration, Inhalation↗
PubMed1988

Effect of morphine on self-stimulation in rats and its modification by chloramphenicol.

The effect of morphine was studied on self-stimulation (SS) behavior in rats implanted with bipolar electrodes in the posterior hypothalamus. A single dose (10 mg/kg) of morphine decreased SS responding within 10-20 min, reaching a minimum level between 20-40 min after which the responding gradually returned to normal. The SS responding then increased above the control level at 120-180 min postdrug, then slowly returned to normal, thus showing a rebound effect. The combination treatment with morphine (10 mg/kg) and chloramphenicol (50 mg/kg) on SS behavior produced an accentuation of the initial decrease in responding, which was prolonged before gradually returning to the control levels without showing any rebound effect. The data suggest that alterations in protein synthesis may underlie the suppressed excitatory effect of a high dose of morphine on SS behavior.

Animals↗
PubMed1987

Effect of inhalation of xylene on intracranial self-stimulation behavior in rat.

The effect of the inhalation of xylene on intracranial self-stimulation behavior was studied in rats in a flow-through (dynamic) inhalational behavioral chamber. Rats were exposed successively to four graded concentrations (102, 192, 419 and 623 ppm) of xylene vapor during 2-hr sessions on different days. The rate of lever-pressing showed a dose-dependent decrease during exposure to 192, 419 and 623 ppm of xylene. The 4-hr exposure to the smallest concentration (106 ppm) of xylene failed to show any effect on self-stimulation behavior. During a 5-day 2 hr/day exposure, the decrease in response observed on the 1st day was further accentuated with a nadir on the 3rd day; from the 4th day onwards, the depressant effect was attenuated showing the development of tolerance.

Administration, Inhalation↗
PubMed1987

Effect of xylene inhalation on fixed-ratio responding in rats.

The effect of xylene inhalation was studied on operant behavior under a fixed-ratio (FR24) schedule in rats. Experiments were performed while rats were being exposed to xylene vapor in an inhalational (flow-through) behavioral chamber. Rats were exposed successively to three graded concentrations (113, 216 and 430 ppm) of xylene vapor each for 2 hr in range-finding studies during 6 1/4-hr sessions. The reinforcement rate which is correlated with FR responding was shown to be decreased at hr 1, hr 3 and hr 5. However at hr 2, hr 4 and hr 6 the reinforcement rate in rats increased approaching the control levels, thereby indicating development of tolerance. When rats were exposed to one of the three graded concentrations of xylene for 2 hr on separate days, they also showed a decrease in the reinforcement rate at hr 1; development of acute tolerance was also noted in this schedule. Exposure to the lowest (98.5 ppm) level of xylene used during 5-hr sessions caused no significant decrease in the reinforcement rate. This study thus attempts to identify a minimum effective concentration of xylene and indicates the development of acute tolerance to behavioral effect of xylene.

Administration, Inhalation↗
PubMed1986

An inhalational behavioral chamber.

An inhalational (flow-through) behavioral chamber has been designed and prepared in order to facilitate recording of the behavioral performance of a small experimental animal (e.g., rat and mouse) while the subject is being exposed to an inhalant (vapor or gas). The animal can be clearly viewed during behavioral performance inside the chamber, which consists of a cylindrical glass jar. The apparatus is made up of easily available materials (e.g., glass, metal, Teflon, etc.) that are not affected by usual industrial solvents. At the present stage of its development, three types of behavioral schedules can be performed within the chamber: schedules involving brain stimulation (e.g., self-stimulation, avoidance of aversive stimulations); liquid-reinforced schedules (e.g., fixed ratio, fixed interval, variable ratio, variable interval, differential reinforcement of low rates); shock avoidance (classical or continuous). The schedules can be microcomputer assisted. The device is suitable for study of behavioral pharmacology and toxicology of inhalants.

Animals↗
PubMed1985

Long-term desipramine treatment attenuates clonidine-induced suppression of ventral tegmental self-stimulation.

Long-term administration of the tricyclic antidepressant desipramine did not change the rate of self-stimulation responding in the A10 (ventral tegmental) area but significantly attenuated the suppressive effect of the selective alpha 2-adrenergic agonist clonidine on this behavior. These findings demonstrate an involvement of noradrenergic mechanisms in the regulation of ventral tegmental self-stimulation and further suggest that adaptive changes in inhibitory presynaptic noradrenergic receptors may be involved in desipramine's antidepressant effects.

Animals↗
PubMed1984

Phencyclidine (PCP): some human studies.

Studies on the effects of PCP have been conducted in volunteers in the Army Laboratories and elsewhere and in illicit users. The present review has summarized the observations of many investigators which showed that the acute effects of PCP following several routes of administration were shown to be dose-related. High doses of PCP produce disturbing manifestations including psychosis, numbness, light-headedness, vertigo, ataxia, and nystagmus due to acute intoxication. Furthermore, some subjects became irritable, argumentative or negative under the conditions of social stress and demanding tasks. In addition to a variety of central action, PCP has also been shown to affect cardiovascular function, heat storage, and exercise performance. PCP can also induce, although rarely, prolonged toxic psychosis in chronic abusers and precipitate psychotic episodes in psychotic and prepsychotic personalities. Tolerance, but not physical dependence, develops to the effects of PCP. Psychologic dependence as indicated by craving for the drug has however been reported.

Administration, Oral↗
PubMed1984

Pharmacology of some synthetic tetrahydrocannabinols.

DMHP (1-hydroxy-3-1', 2'-dimethylheptyl-6,6,9-trimethyl 7,8,9,10-tetrahydro-6-dibenzopyran or in brief dimethyl heptyl pyran, EA 1476) is a synthetic analog of delta 9-tetrahydrocannabinol (delta 9-THC). Both DMHP and its acetate, DMHPA (EA 2233) produce varying degrees of physical and mental incapacitation. Both compounds elicit orthostatic hypotension at dose levels far below those required to produce mild mental incapacitation. Compared with delta 9-THC, DMHP has clearly more potent and prolonged hypotensive action, but much less psychological effect. The potencies of DMHP and DMHPA are more or less similar, but the acetate derivative is more stable against the degrading effects of light and air. Like DMHP, DMHPA consists of eight isomers which vary in their potency. Accordingly, depending on the proportion of the isomers, the racemic mixtures show variability in their potencies. The isomers 2 and 4 have been shown to be more potent than the other isomers.

Animals↗
PubMed1983

Self-stimulation responses are altered following long-term but not short-term treatment with clorgyline.

Clorgyline (a selective monoamine oxidase-inhibiting antidepressant) given chronically facilitated hypothalamic self-stimulation in rats, while acute treatment was without effect. Furthermore, long-term but not short-term clorgyline treatment significantly attenuated the suppressive effect of the selective alpha 2-adrenergic agonist clonidine on this behavior. These findings suggest that adaptative alterations in the modulation of rewarded behavior by inhibitory presynaptic noradrenergic receptors may be involved in antidepressant efficacy.

Animals↗
PubMed1981

Behavioral and neurochemical effects of hydergine in rats.

Effects of various (20, 40 or 80 mg/kg; intragastric instillation) doses of Hydergine (dihydroergotoxine) were studied on the self-stimulation (SS) behavior (in young and old rats with electrodes implanted in the A10 area) and also on spontaneous motor activity (SMA) and stereotypy (ST) as well as on the concentrations of norepinephrine (NE), dopamine (DA), serotonin (5-HT) and gamma-aminobutyric acid (GABA) in discrete brain areas, such as caudate nucleus (CN), pons-medulla (PM) and diencephalon-midbrain (DM) in adult rats. Following Hydergine administration, SS and SMA showed a dose-dependent increase with peak effects occurring between 80-120 min and then decreased. ST was not induced at any dose. DA and NE levels in the DM also showed a dose-dependent increase at 90 min and then sharply decreased up to 120 min after drug administration. NE in the PM and DA in the CN showed a similar pattern, but to a smaller degree. GABA in the DM and CN showed marked increases up to 120 min, while 5-HT in the PM and DM showed steady declines during the same period. Thus it appears that the behavioral stimulant effects of Hydergine may be correlated to increase in NE and DA levels, particularly in the DM.

Animals↗