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1.
Indian J Physiol Pharmacol ; 2004 Jan; 48(1): 51-8
Artículo en Inglés | IMSEAR | ID: sea-106469

RESUMEN

The present study was carried out in five cats which did not attack the rats spontaneously. Predatory attack on an anaesthetized rat was elicited by electrical stimulation of extreme lateral regions of hypothalamus. These sites were stimulated at a current strength from 300-700 microa to evoke a predatory attack on an anaesthetized rat. The attack was accompanied by minimal affective display such as alertness, pupillary dilatation, and culminated in beck biting at higher current strength. A scoring system allowed the construction of stimulus response curves, which remained fairly constant when repeated over a period of 3-4 weeks. Microinfusions of norepineprine and clonidine in 4.0 and 5.0 microg dose respectively in locus ceruleus and adjoining tegmental fields facilitated the predatory attack and there was a significant reduction in the threshold current strength for the elicitation of affective and somatomotor components. Microinfusions of yohimbine, an alpha-2 blocker, in 5 microg dose completely blocked the predatory attach response as indicated by an increase in the threshold current strength for the affective components. The somatomotor components were completely inhibited and could not be elicited even when the current strength was increased to 1000 microA. The predatory attack behavior remained completely inhibited for almost two hours following microinfusion of yohimbine. During this period, the animal was extremely drowsy and reacted very slowly even to a painful stimulus such as pinching of tail. Microinfusions of propranalol (beta-blocker), practalol (beta-1 blocker), prazosin (alpha-1 antagonist), propylene glycol as well as saline in similar volumes (0.5 microl) as control failed to produce any blocking effect, thus indicating the involvement of alpha-2 adrenoceptive mechanisms in the modulation of predatory attack in this region of midbrain. The facilitatory effects of norepinephrine and clonidine were significant at P<0.01 and P<0.05 respectively with Wilcoxon's signed rank test. The inhibitory effects of yohimbine were significant at P<0.05. The present study indicates the involvement of alpha-2 adrenoceptive mechanisms in the facilitation of hypothalamically elicited predatory attack.


Asunto(s)
Agonistas alfa-Adrenérgicos/administración & dosificación , Antagonistas Adrenérgicos alfa/farmacología , Animales , Gatos , Clonidina/farmacología , Estimulación Eléctrica , Electrodos Implantados , Femenino , Hipotálamo/fisiología , Locus Coeruleus/fisiología , Masculino , Microinyecciones , Norepinefrina/administración & dosificación , Conducta Predatoria/fisiología , Receptores Adrenérgicos alfa 2/antagonistas & inhibidores , Sistema Nervioso Simpático/fisiología , Yohimbina/farmacología
2.
Indian J Physiol Pharmacol ; 2003 Jul; 47(3): 311-7
Artículo en Inglés | IMSEAR | ID: sea-106779

RESUMEN

The present study was carried out in five cats which did not attack the rats spontaneously. Predatory attack on an anaesthetized rat was elicited by electrical stimulation of lateral hypothalamus at a mean current strength of 650 microA. The attack was accompanied by minimal affective display and culminated in neck biting. Microinfusions of DAME (delta-alanine methionine enkephaline) in 500 ng dose in substantia nigra facilitated the predatory attack and there was a significant reduction in the threshold current strength for affective display as well as somatomotor components. Microinfusions of naloxone, an opioid antagonist in 1.0 microg dose when DAME effect was at its peak reversed the facilitatory effects and the threshold returned to the control levels within 10 minutes of naloxone infusion at the same locus. Microinfusions of naloxone alone in similar dosage completely blocked the predatory attack response as indicated by an increase in the threshold current strength for somatomotor as well as affective display components. The somatomotor were completely inhibited and could not be elicited even when the current strength was increased to 1000 microA. Control injections of saline in similar volumes (0.5 microl) failed to produce any response Microinfusions of naloxone in lower dose (250 ng) failed to produce any blocking effect. These findings indicate that hypothalamically elicited predatory attack is facilitated by enkephalinergic mechanisms operating at the midbrain level.


Asunto(s)
Agresión/efectos de los fármacos , Animales , Gatos , Relación Dosis-Respuesta a Droga , Estimulación Eléctrica , Electrodos Implantados , Encefalina Metionina/administración & dosificación , Encefalinas/administración & dosificación , Femenino , Hipotálamo/anatomía & histología , Masculino , Microinyecciones , Naloxona/administración & dosificación , Antagonistas de Narcóticos/administración & dosificación , Conducta Predatoria/fisiología , Sustancia Negra/anatomía & histología
3.
J Postgrad Med ; 2001 Jan-Mar; 47(1): 55-61
Artículo en Inglés | IMSEAR | ID: sea-116717

RESUMEN

Panic Disorder and agoraphobia offer considerable diagnostic and management challenges, particularly in general practice. We describe a typical case of panic disorder in a young adult. The recent advances in our understanding of brain functions can be used to explain to a certain extent the biologic basis of panic disorder. A hypothetical model integrating current views on panic disorder and agoraphobia has been proposed. The management principles including the role of cognitive therapy and pharmacotherapy have been discussed.


Asunto(s)
Adulto , Agorafobia/fisiopatología , Ansiedad , Humanos , Masculino , Modelos Neurológicos , Trastorno de Pánico/diagnóstico
4.
Indian J Exp Biol ; 2000 Aug; 38(8): 834-6
Artículo en Inglés | IMSEAR | ID: sea-62004

RESUMEN

Food deprivation produces analgesia. This response is reversed i.e. pain sensitivity is lowered, when the food deprived rats are fed. In the present study the effect of chronic pain on the motivation to get food, in food deprived rats, was observed. In ten rats the effect of formalin and morphine plus formalin on the motivation to get food was studied. Injection of formalin significantly (P < 0.01) decreased the number of lever presses from 450 +/- 30 to 225 +/- 25. However, after injecting morphine the effect was reversed. The present study shows reduced internal drive to procure food by the food deprived animals, when they were under chronic pain. The effect was blocked by morphine, suggesting the role of opioids in modulating the motivation for getting food.


Asunto(s)
Animales , Conducta Alimentaria , Masculino , Morfina/administración & dosificación , Dolor/fisiopatología , Ratas , Ratas Wistar
5.
Indian J Physiol Pharmacol ; 1999 Oct; 43(4): 449-57
Artículo en Inglés | IMSEAR | ID: sea-108177

RESUMEN

Central pathways transmit pain from peripheral regions to one of the most important area of the descending pain modulatory system, the Periaqueductal gray (PAG). Independent discoveries in the past suggest that the PAG contains afferent input, output neurons and intrinsic interneurons. An attempt was made in the present study to find out the effects of more than one kind of noxious stimulus on the PAG neuronal activity. Experiments were conducted in rhesus monkeys and the effects of noxious mechanical, thermal and tooth-pulp stimulation on the activity of 14 neurons were studied. The neurons responded to more than one kind of noxious stimuli by increasing or decreasing its firing rate. No limb specificity could be identified and homogeneous distribution of the excitatory and inhibitory neurons was found.


Asunto(s)
Animales , Pulpa Dental/fisiología , Estimulación Eléctrica , Electrofisiología , Calor/efectos adversos , Macaca mulatta , Masculino , Sustancia Gris Periacueductal/fisiología , Nervios Periféricos/fisiología , Estimulación Física
6.
Indian J Physiol Pharmacol ; 1999 Jul; 43(3): 323-31
Artículo en Inglés | IMSEAR | ID: sea-108301

RESUMEN

The hypothalamo-limbic system has been implicated in recognizing the affective significance of pain and elicitation of related emotional responses. Several evidences from different studies support a role of these areas in endogenous analgesic mechanisms for pain modulation as elucidated by different pain tests in more than one animal model. In the above context, the aim of this study was to investigate the relative effectiveness of the pain modulatory action of hypothalamic and limbic structures in rat using similar stimulation parameters, and studying the effect on tooth pulp stimulation evoked jaw opening reflex (TP-JOR). To achieve the objective, unilateral stimulation of hypothalamic (lateral = LH; ventromedial = VMN; anterior = AH) and limbic areas (amygdala = AMYG; hippocampus = HIPP) was done on the TP-JOR test. A significant reduction in the amplitude of EMG recorded from the digastric muscle (dEMG) as a result of tooth-pulp stimulation was observed on stimulation of LH, VMN, AMYG and HIPP but not from AH. Also, the magnitude of this effect was almost similar from these areas. The results suggest that these areas (except AH) have an antinociceptive role in tooth-pulp stimulation evoked pain response.


Asunto(s)
Amígdala del Cerebelo/fisiología , Animales , Pulpa Dental/fisiología , Estimulación Eléctrica , Electromiografía , Hipocampo/fisiología , Área Hipotalámica Lateral/fisiología , Hipotálamo/fisiología , Sistema Límbico/fisiología , Masculino , Nociceptores/fisiología , Dimensión del Dolor , Ratas , Ratas Wistar , Reflejo/fisiología , Núcleo Hipotalámico Ventromedial/fisiología
7.
Indian J Exp Biol ; 1997 May; 35(5): 438-42
Artículo en Inglés | IMSEAR | ID: sea-57139

RESUMEN

Present study was carried out in nine cats which did not attack the rats spontaneously. Predatory attack on an anaesthetized rat was elicited by electrical stimulation of lateral hypothalamus at a mean current strength of 690 microA. The attack was accompanied by minimal affective display and culminated in neck biting. Microinjections of delta-alanine methionine enkephaline (DAME) in 250 ng dose in dorsal periaqueductal gray completely suppressed the predatory attack. There was a significant increase in the threshold current strength for affective display components while the somatic components were completely inhibited even when the current strength was increased to 1000 microA. Microinjections of naloxone, an opioid antagonist in 1 microgram dose reversed the DAME blocking effect and the thresholds returned to control levels within 10 min of microinjections. Microinjections of naloxone alone in similar dose facilitated the response as indicated by a decrease in threshold current strengths for both affective display and somatomotor components. Control injections of saline in similar volumes (0.5 microliter) failed to produce any change. These findings indicate that hypothalamically induced predatory attack is inhibited by enkephalinergic mechanisms operating at the dPAG level in the midbrain.


Asunto(s)
Animales , Gatos , Encefalinas/fisiología , Femenino , Hipotálamo/fisiología , Masculino , Sustancia Gris Periacueductal/fisiología , Conducta Predatoria/fisiología , Ratas
8.
Indian J Physiol Pharmacol ; 1997 Apr; 41(2): 116-22
Artículo en Inglés | IMSEAR | ID: sea-106739

RESUMEN

Bipolar concentric electrodes were implanted in five cats in extreme lateral regions of hypothalamus. These sites were electrically stimulated using biphasic square wave pulses at a current strength ranging from 300-800 microA to evoke predatory attack on an anaesthetized but live rat. At lower current strength (300 microA) only alertness with pupillary dilatation was produced. Gradual increase in the current strength led to the recruitment of somatic and affective components and a predatory attack was exhibited at a mean current strength of 700 microA. A scoring system allowed the construction of stimulus response curves, which remained fairly constant when repeated over a period of 3-4 weeks. Bilateral microinjections of delta-alanine methoinine enkephaline (DAME) (500 ng in 0.5 microliter saline) in ventrolateral tegmental area (VTA) elevated the mean threshold current strength for affective components while somatomotor components were totally inhibited. The blocking effect of DAME persisted for 1 hour. Microinjections of naloxone (1 microgram) in similar volumes facilitated the response as indicated by a reduction in threshold current strength for somatomotor and affective components. Microinjections of naloxone (1 microgram) in similar volumes facilitated the response as indicated by a reduction in threshold current strength for somatomotor and affective components. Microinjections of naloxone (1 microgram) also reversed the blocking effect of DAME and the thresholds returned to the control level within 10 min while microinjection of normal saline as control had no effect. The excitatory effects of naloxone and inhibitory effects of DAME were statistically significant at P < 0.01 and P < 0.05 respectively with Wilcoxon's signed rank test. The present study indicates that enkephalinergic as well as opioidergic mechanisms operating at the midbrain (VTA) level are involved in the inhibition of predatory attack as elicited from lateral hypothalamus.


Asunto(s)
Animales , Gatos , Interacciones Farmacológicas , Estimulación Eléctrica , Electrodos Implantados , Encefalina Metionina/administración & dosificación , Encefalinas/fisiología , Femenino , Hipotálamo/efectos de los fármacos , Masculino , Microinyecciones , Naloxona/administración & dosificación , Antagonistas de Narcóticos/administración & dosificación , Conducta Predatoria/efectos de los fármacos , Ratas , Coloración y Etiquetado , Área Tegmental Ventral/efectos de los fármacos
9.
Indian J Exp Biol ; 1997 Apr; 35(4): 332-7
Artículo en Inglés | IMSEAR | ID: sea-56529

RESUMEN

Bipolar concentric electrodes were implanted in extreme lateral regions of hypothalamus having coordinates (A12.5 mm, L 3.5-3.7 mm, V 3.0-3.7 mm). These sites were electrically stimulated using biphasic square wave pulses (1 ms, 60 Hz) at a current strength ranging from 300-800 microA to evoke predatory attack on an anaesthetized rat. At lower current strengths of 300 microA only altertness with pupillary dilatation was produced. Gradual increase in the current strength led to recruitment of somatic and affective components and a full blown predatory attack on a rat was produced at a mean current strength of 700 microA. A scoring system allowed the construction of stimulus response curve, which remained fairly constant when repeated over a period of 3-4 weeks. In ventrolateral tegmental area (VTA), bilateral microinjections of norepinephrine (NE 10 micrograms in 0.5 microliter saline, pH 7.4) lowered the mean threshold current strength to 100 microA while predatory attack was produced at 500 microA. Clonidine (5 micrograms in 0.5 microliter propylene glycol, pH 7.4) an alpha-2 agonist similarly lowered the mean threshold to 100 microA and predatory attack threshold to 400 microA. The effects of clonidine appeared within 20 min of microinjection and persisted up to 6 hr. Yohimbine, an alpha-2 antagonist (4 micrograms in 0.5 microliter propylene glycol. pH 7.4) when microinjected into the same locus (VTA), completely blocked predatory attack behaviour for 3 days, the peak period of the blocking effects were between 3-8 hr, after microinjection. Isoproterenol (beta agonist), propranolol (beta blocker), prazosin (alpha-1 antagonist) and phenoxybenzamine (alpha antagonist) failed to produce any effect. Normal saline and propylene glycol in similar volumes served as controls. The excitatory effects of NE and clonidine and inhibitory effects of Yohimbine were significant at P < 0.01 and P < 0.05 respectively with Wilcoxon's signed rank test. The present study indicates the involvement of alpha-2 adrenoceptive mechanisms operating at the midbrain (VTA) level in the elicitation of predatory attack from lateral hypothalamus.


Asunto(s)
Agonistas alfa-Adrenérgicos/farmacología , Animales , Gatos , Clonidina/farmacología , Femenino , Hipotálamo/fisiología , Masculino , Norepinefrina/farmacología , Conducta Predatoria/efectos de los fármacos , Ratas , Receptores Adrenérgicos alfa 2/efectos de los fármacos , Área Tegmental Ventral/fisiología
10.
Indian J Physiol Pharmacol ; 1996 Oct; 40(4): 289-96
Artículo en Inglés | IMSEAR | ID: sea-107356

RESUMEN

Naloxone has been reported to affect pain and locomotor activity differently depending on the dose. The objective of the present investigation was to study the effects of low and high (6 micrograms and 3 mg/kg, s.c.) doses of naloxone (Nx) on formalin-induced pain (tonic pain) and spontaneous motor activity and any correlation between them. The experiments were conducted on adult male Wistar rats. Tonic pain and spontaneous motor activity were recorded by the formalin test and video monitoring respectively. An increase in spontaneous motor activity (locomotion, movements and distance) was observed following formalin injection as compared to basal activity (P < 0.05). Low dose of Nx reduced the pain intensity and also the spontaneous motor activity during the later phase (after 15 min of formalin injection) (P < 0.05). High dose of Nx on the other hand increased the pain intensity but still reduced motor activity (P < 0.05). Both doses of Nx initially produced hyperalgesia (5 min peak). The bidirectional effects of Nx on formalin pain were dissociated from the spontaneous motor behavior of rats. A direct correlation could not be established between pain intensity and spontaneous motor activity.


Asunto(s)
Animales , Conducta Animal/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Formaldehído , Masculino , Actividad Motora/efectos de los fármacos , Naloxona/farmacología , Antagonistas de Narcóticos/farmacología , Nociceptores/efectos de los fármacos , Dolor/inducido químicamente , Ratas , Ratas Wistar
11.
Indian J Physiol Pharmacol ; 1995 Oct; 39(4): 339-46
Artículo en Inglés | IMSEAR | ID: sea-108517

RESUMEN

The limbic system has been implicated in the modulation of pain. The aim of this study was to determine the role of amygdala in different types of pain, viz., phasic and tonic. Unilateral stimulation of central nucleus of amygdala (CeA), basolateral nucleus (BL) and medial amygdaloid (MeA) in conscious rats resulted in the reduction of the tonic formalin-induced pain. The thresholds for simple vocalization (SV) and vocalization after-discharge (VA) were elevated during amygdalar stimulation in the tail-flick (phasic pain) test. However, the threshold for tail-flick (TF) evoked by electric shock was not affected. Tail-flick latency (TFL) to noxious heat was accentuated during amygdalar stimulation. These results suggest that amygdala had a modulatory role in the descending endogenous pain control mechanisms.


Asunto(s)
Amígdala del Cerebelo/anatomía & histología , Animales , Estimulación Eléctrica , Emociones/fisiología , Formaldehído/diagnóstico , Masculino , Dolor/fisiopatología , Dimensión del Dolor , Umbral del Dolor/fisiología , Ratas , Tiempo de Reacción/fisiología , Vocalización Animal/efectos de los fármacos
12.
Indian J Physiol Pharmacol ; 1994 Jul; 38(3): 181-4
Artículo en Inglés | IMSEAR | ID: sea-108812

RESUMEN

Electromagnetic fields (EMFs) affect the metabolism of the body including the nervous, endocrine, cardiovascular, hematological as well as the reproductive system. EMFs are environmental pollutants, thus posing a health hazard which can cause steric changes in the molecule located at the cell surface. Microwaves are known to cause chromosomal abberations and act as tumor promoters. The process involves a stream of signals from cell membrane to nucleus and other organelles. The present investigations aim to understand the mechanism of biological effects of microwaves (2.45 GHz). The effect was studied on poly ADP-ribosylation, which is a post translational modification of chromatin protein catalysed by the enzyme poly ADPR polymerase using NAD+ as the substrate. Poly ADP-ribosylation has been shown to be involved in several aspects of chromatin structure and function. Twenty-three days old rats weighing 42-48 gms were exposed at a microwave dose level of 1.0 mW/cm2. After exposure for sixty days the animals were sacrificed and an estimation of poly ADPR polymerase activity was undertaken in different organs of these animals. There was an increase of 20% in its activity in liver, 35% in testis, whereas brain showed a 53% decrease in diencephalon and 20% decrease in the cortex in the exposed animals as compared to their respective controls. There was no change in enzyme activity in spleen and kidney. This was accompanied by concomitant changes in NAD+ levels. The above results may be cited as important events in carcinogenesis and tumor promotion related to microwave exposure and the signal transduction mechanism involved. The goal is to shed light on complex ecogenetic interactions leading to cancer modulation of gene expression by epigenetic mechanism.


Asunto(s)
Animales , Encéfalo/enzimología , Electroforesis en Gel de Poliacrilamida , Riñón/enzimología , Hígado/enzimología , Masculino , Microondas/efectos adversos , NAD/efectos de la radiación , Poli(ADP-Ribosa) Polimerasas/efectos de la radiación , Ratas , Ratas Wistar , Bazo/enzimología , Testículo/enzimología , Distribución Tisular
13.
Indian J Physiol Pharmacol ; 1993 Jul; 37(3): 189-93
Artículo en Inglés | IMSEAR | ID: sea-107281

RESUMEN

The present study was designed to characterise the analgesia produced by the GABA B agonist baclofen in tonic pain in monkeys. The effect of various doses of baclofen was studied on formalin induced pain. Baclofen was injected intraperitoneally 30 min prior to formalin injection in five doses of 2, 4, 6, 8, and 10 mg/kg and the pain was quantified for a period of one hour. Baclofen produced dose related analgesia, 6 mg/kg having maximal effect. The antinociceptive effect of baclofen could be attributed to the effect of baclofen on GABA B receptors producing presynaptic inhibition of primary nociceptive afferents in the dorsal horn of the spinal cord.


Asunto(s)
Analgésicos/farmacología , Animales , Baclofeno/farmacología , Relación Dosis-Respuesta a Droga , Formaldehído , Macaca mulatta , Masculino , Dolor/inducido químicamente , Dimensión del Dolor/efectos de los fármacos , Receptores de GABA-B/efectos de los fármacos
14.
Indian J Physiol Pharmacol ; 1993 Apr; 37(2): 127-31
Artículo en Inglés | IMSEAR | ID: sea-108587

RESUMEN

The present study was carried out in ten cats of either sex. Flight response was obtained by electrical stimulation of dorsomedial regions of preoptic area (A13-14.5, L3.5 V-3.5 to -3.7) and lateral hypothalamic regions (A12.5, L2.5-3.5, V-3.7). It consisted of a goal directed attempt to get out of the cage with a vigorous leaping to foot. Norepinephrine when microinjected in 10 micrograms doses into pretectal area of midbrain (A3.5, 3.0, V+1.0 to +1.5 mm) significantly lowered the mean current strength from 640uA to 420uA; clonidine, an alpha-2 agonist in 5 micrograms dose when microinjected into the same locus also significantly lowered the mean current strength to the same level. On the other hand yohimbine, an alpha-2 blocker in 5 micrograms dose when microinjected in to the same locus significantly increased the mean current strength from 640 to 970 uA. These results indicate that hypothalamically induced flight response is mediated via the alpha-2 adrenoceptive mechanism operating at the midbrain level. Control microinjection of normal saline and propylene glycol in similar volumes failed to produce any changes in current strength.


Asunto(s)
Agonistas alfa-Adrenérgicos/farmacología , Antagonistas Adrenérgicos alfa/farmacología , Animales , Gatos , Estimulación Eléctrica , Reacción de Fuga/efectos de los fármacos , Femenino , Hipotálamo/efectos de los fármacos , Masculino , Sustancia Gris Periacueductal/efectos de los fármacos , Receptores Adrenérgicos alfa 2/fisiología
15.
Indian J Physiol Pharmacol ; 1993 Apr; 37(2): 121-6
Artículo en Inglés | IMSEAR | ID: sea-107550

RESUMEN

The present study was carried out in ten cats which did not attack the rats spontaneously. Predatory attack on a rat was produced by lateral hypothalamic stimulation using mean current strength of 340-690uA. This attack was accompanied by minimal affective display and culminated in neck biting. It was found that norepinephrine (NE) when microinjected into dorsal periaqueductal gray (dPAG) region in doses of 2, 4 and 10ug significantly lowered the mean current strength required for the elicitation of predatory attack by hypothalamic stimulation. Microinjection of propranolol (Prop), a beta-blocker, within the same region in similar doses significantly blocked the response as indicated by the increase in current strength required to produce the response. Control injections of normal saline and propylene glycol failed to produce any change. These findings indicate that hypothalamically induced aggressive responses involves beta adrenoceptive mechanisms located in the dPAG.


Asunto(s)
Agonistas alfa-Adrenérgicos/farmacología , Antagonistas Adrenérgicos beta/farmacología , Animales , Gatos , Relación Dosis-Respuesta a Droga , Estimulación Eléctrica , Femenino , Hipotálamo/efectos de los fármacos , Masculino , Sustancia Gris Periacueductal/fisiología , Conducta Predatoria/efectos de los fármacos , Ratas , Receptores Adrenérgicos beta/fisiología
16.
Indian J Physiol Pharmacol ; 1992 Jan; 36(1): 21-8
Artículo en Inglés | IMSEAR | ID: sea-108737

RESUMEN

Although it is known that protein, fat and fibre reduce the postprandial glycaemia following an oral carbohydrate load, the nature and extent of interaction of different nutrients with one another in this respect is not well understood. The present study was designed to explore systematically the glycaemic and insulinaemic response to glucose (G) alone, or in combination with one or more of the following: casein (CS), maize oil (MO), cellulose (CL) and pectin (P). Besides 100 g G, eleven isoenergetic and six isocarbohydrate meals were studied on healthy adult males using an incomplete block design. Addition of other nutrients to G led to a lowering of the glycaemic response. The lowest glycaemic responses were seen in case of meals containing the largest number of nutrients. P was more effective in reducing postprandial glycaemia than CL. As in case of glycaemic response, low insulinaemic responses were also associated with P-containing meals, and meals containing the largest number of nutrients. But unlike in case of glycaemic response, there was a tendency for elevation of the insulinaemic response in case of CL-containing meals. The degree of attenuation of glycaemic response observed with meals containing several nutrients was roughly predictable on the basis of the attenuation observed with meals in which only one nutrient had been added at a time to G. But the glycaemic response of natural foods is unlikely to be predictable on the basis of their nutrient composition because of the overriding influence of several other factors such as physical form, cooking, processing, storage and antinutrient content of the food.


Asunto(s)
Adolescente , Adulto , Glucemia/metabolismo , Caseínas/farmacología , Celulosa/farmacología , Dieta , Fibras de la Dieta/farmacología , Proteínas en la Dieta/farmacología , Interacciones Farmacológicas , Glucosa/farmacología , Humanos , Insulina/sangre , Masculino , Valor Nutritivo , Pectinas/farmacología
17.
Indian J Exp Biol ; 1991 Aug; 29(8): 744-50
Artículo en Inglés | IMSEAR | ID: sea-56127

RESUMEN

Neocortex and hippocampus play important role in motor activity, neuronal plasticity and learning and memory mechanisms. Electroencephalographic (EEG) activity of neocortex and hippocampus of rat following NMDA-receptor agonist, N-methyl-D-aspartate (NMDA), 0.25-2 nmol in 10 microliters, ICV and noncompetitive NMDA-receptor antagonists, MK 801 (0.025-0.1 mg/kg, ip) and ketamine (10-50 mg/kg, ip) at OH, 1/2H, 4H, 8H and 24H was recorded. The electrodes were implanted stereotaxically in hippocampus and neocortex respectively. NMDA (0.25 and 1 nmol) showed longer lasting decrease in amplitude in hippocampus and in frequency in cortical neurons while 2 nmol produced epileptogenic neurotoxicity. Opposite effect i.e. increase in amplitude in both, hippocampus and neocortex was observed with MK 801 and ketamine and these agents also showed longer lasting influence. Administration of MK 801 (0.05 mg/kg) and ketamine (50 mg/kg) prior to NMDA 2 nmol protected 40% animals from NMDA-induced neurotoxicity and blockade of NMDA-induced long term influence. The EEG effect of NMDA agonist and NMDA-induced neurotoxicity at higher dose and its modification by NMDA-antagonist, MK 801 and ketamine suggest that beside NMDA agonists (NMDA), its antagonists may, also affect long lasting changes in hippocampus and cortex. These antagonists reverse NMDA-mediated long term influence in these brain areas.


Asunto(s)
Animales , Corteza Cerebral/metabolismo , Maleato de Dizocilpina/farmacología , Electroencefalografía/efectos de los fármacos , Hipocampo/metabolismo , Ketamina/farmacología , Ligandos , Masculino , N-Metilaspartato/metabolismo , Ratas , Ratas Endogámicas , Receptores de N-Metil-D-Aspartato/antagonistas & inhibidores
18.
Indian J Physiol Pharmacol ; 1991 Jul; 35(3): 165-9
Artículo en Inglés | IMSEAR | ID: sea-108233

RESUMEN

Self-aggression is a behavioural disorder in which an individual damages its own body parts by intense biting or scratching. Self aggression has been reported in human patients in Lesch-Nyhan syndrome and in cases of schizophrenia, depression, and congenital analgesia. In human patients as well as in experimental animals some kind of dysesthesia of the part of the body that is mutilated has been suggested. This study was conducted to find out the underlying pain mechanisms in self-aggressive behaviour arising out of stereotypy. The study was performed in 40 adult male rats. In all these animals, self-aggression was produced as part of amphetamine induced stereotyped behaviour. A predetermined scale was used for quantifying this behaviour. Reserpine and phenoxybenzamine pretreatment led to an increase in the incidence of self-aggression. Naloxone administration in reserpine pretreated animals led to a further significant increase in the incidence of self biting as compared to controls. From these studies it appears that self-aggressive behaviour may be associated with increased pain sensation.


Asunto(s)
Agresión/efectos de los fármacos , Anfetamina/farmacología , Animales , Conducta Animal/efectos de los fármacos , Masculino , Naloxona/farmacología , Norepinefrina/fisiología , Dolor/fisiopatología , Fenoxibenzamina/farmacología , Ratas , Receptores Opioides/efectos de los fármacos , Reserpina/farmacología , Automutilación/fisiopatología , Factores de Tiempo
19.
Indian J Physiol Pharmacol ; 1991 Apr; 35(2): 111-6
Artículo en Inglés | IMSEAR | ID: sea-106890

RESUMEN

Electroencephalographic (EEG) activity in neocortex of rats following intracerebroventricular (icv) administration of NMDA (0.25-2 nmol/10 microliters) and its modification by noncompetitive NMDA-receptor antagonists, dizocilpine (MK-801) (0.025-0.1 mg/kg, ip) and ketamine (10-50 mg/kg, ip) was recorded at 0, 0.5, 4, 8 and 24 hr with chronically implanted electrodes. NMDA (0.25 and 1 nmol) showed longer lasting decrease in frequency in cortical neurons while 2 nmol produced convulsions and death. Administration of MK 801 (0.05 mg/kg) and ketamine (50 mg/kg) prior to NMDA offered protection in 40% of animals against NMDA-induced convulsions and blocked NMDA-induced long term influence. However, ketamine and MK 801 showed an increase in percent amplitude and also had long lasting effects per se. In conscious mice, NMDA (0.5-10 nmol/microliters icv) induced dose dependent convulsions. Both MK 801 and ketamine showed potent anticonvulsant effect. Ethanol (0.5-2 g/kg, ip) also offered significant protection against NMDA-induced convulsions. MK 801 (0.1 mg/kg) when administered concurrently with ethanol (0.5 g/kg) exhibited synergistic anticonvulsant effect. The EEG study in rats and effect of NMDA in conscious mice provide a direct evidence for the role of NMDA-receptor system in convulsions and in anticonvulsant action of ethanol.


Asunto(s)
Animales , Corteza Cerebral/efectos de los fármacos , Maleato de Dizocilpina/farmacología , Electroencefalografía/efectos de los fármacos , Etanol/farmacología , Ketamina/farmacología , Masculino , Ratones , N-Metilaspartato/antagonistas & inhibidores , Ratas , Receptores de N-Metil-D-Aspartato/metabolismo , Convulsiones/inducido químicamente
20.
Indian J Physiol Pharmacol ; 1991 Apr; 35(2): 99-105
Artículo en Inglés | IMSEAR | ID: sea-107503

RESUMEN

The present study was designed to examine the effect of corn oil (Co) on postprandial glycaemia and insulinaemia when ingested with glucose (G), casein (Cs), cellulose (Cl) and pectin (P) in various combinations. The study was conducted on six healthy male volunteers, on each of whom six meal tolerance tests were performed. The meals were isocaloric and consisted of G; G and Co; G, Co and Cs; G, Co and P; G, Co, Cs and P; and G, Co, Cs and Cl. The meals were administered after an overnight fast. In addition to a fasting blood sample, blood was collected 0.5, 1.0, 1.5 and 2.0 h after ingestion for measurement of serum glucose and insulin levels. The glycaemic response to GCo was comparable to that to G, but the insulinaemic response was significantly lower. The glycaemic response to GCoCs was significantly lower than that to G but the insulinaemic response to both was comparable. The cellulose containing meal GCoCsCl showed a further reduction in the glycaemic response but not in the insulinaemic response. The pectin containing meals GCoP and GCoCsP gave the lowest glycaemic and insulinaemic responses, the responses to the latter being lower. Corn oil by itself has only a modest effect on the postprandial metabolic response to glucose. Addition of protein and fibre, specially pectin, leads to significant attenuation of glycaemic and insulinaemic responses.


Asunto(s)
Adulto , Glucemia/metabolismo , Celulosa/metabolismo , Aceite de Maíz/metabolismo , Grasas de la Dieta/metabolismo , Fibras de la Dieta/metabolismo , Proteínas en la Dieta/metabolismo , Ingestión de Alimentos , Prueba de Tolerancia a la Glucosa , Humanos , Insulina/sangre , Masculino , Pectinas/metabolismo , Factores de Tiempo
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