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   1982| October-December  | Volume 14 | Issue 4  
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Effect of caffeine and dextro-amphetamine on muscle strength and physical endurance in albino rats: A Bio-chemical study.
K Jain, FSK Barar
October-December 1982, 14(4):333-340
Caffeine exhibited significant improvement in swimming endurance performance and pulling strength, while d-amphetamine showed improvement in swimming performance only, and insignificantly reduced the pulling strength in rats. Neither of the two drugs suppressed blood lactic acid (BLA) levels, or replenished skeletal-muscle glycogen (SMG) stores. In this study there was no correlation between the "anti-fatigue" action and BLA rise antagonism, which otherwise is an important mechanism involved in the increase of endurance performance. The findings have been discussed in view of available literature.
[ABSTRACT]   Full text not available  [PDF]
  2,019 127 -
Comparison of antidiarrhoeal activity of some drugs in experimental diarrhoea
Yegnanarayan Radha, DS Shrotri
October-December 1982, 14(4):293-299
A number of antidiarrhoeal agents were tried in experimental models of diarrhoea viz., castor oil-induced diarrhoea in rats, serotonin-induced diarrhoea in mice, and cholera toxin hypersecretion in rats. The agents, lidamidine. diphenoxylate+atropine. furazolidine, berberine and belladonna were given as pretreatment before the diarrhoea1 challenge, either singly or in various combinations. Lidamidine was most effective among the agents studied.Combinations except for those with lidamidine, offered no additional advantage over single drugs.
[ABSTRACT]   Full text not available  [PDF]
  1,445 252 -
Metoclopramide in tardive dyskinesia
TJ Hemnani, PG Dashputra, RN Sarda
October-December 1982, 14(4):309-312
The effect of single intravenous doses of metoclopramide ( 10 mg, 20 mg and 40 mg) have been compared with placebo (saline) in a double blind randomised study in 10 patients with tardive dyskinesia, following long term neurokptic therapy. Tardive dyskinesia rating scores were decreased significantly 6 h after administration of meloclopramide (20 mg and 40 mg), when compared with placebo. Reduction of tardive dyskinasia by metoclopramide. ,aD2 receptor- blocking agent, suggest that D2 receptors may be involved in the mediation of this syndrome.
[ABSTRACT]   Full text not available  [PDF]
  1,539 103 -
Effect of baclofen pretreatment on pentobarbitone sleep in mice
VV Joshi, JJ Balsara, AG Chandorkar
October-December 1982, 14(4):341-344
Pretreatment with baclofen, the p-chlorophenyl analogue of GABA, not only prolonged pentobarbitone sleeping time but also induced sleep in mice treated with a subhypnotic dose of pentobarbitone.Probable mechanism involved in the potentiating effect of baclofen on pentobarbitone hypnosis has been discussed on the basis that baclofen by inhibiting the firing of DAergic neurons decreases the activity of the nigrostriatal and mesolimbic DAergic systems involved in cortical activation and behavioural arousal and thus sensitizes the CNS to the depressant action of pentobarbitone. Further, our finding that the subconvulsant dose of picrotoxin, a GABA antagonist, failed to antagonise the potentiating effect of baclofen pretreatment on pentobarbitone hypnosis is in agreement with the report that picrotoxin fails to antagonise the action of baclofen on the DAergic neurons.
[ABSTRACT]   Full text not available  [PDF]
  1,421 94 -
Effect of baclofen pretreatment on the antinociceptive and cataleptic effect of morphine in mice
JJ Balsara, MP Muley, AS Vadya, AG Chandorkar
October-December 1982, 14(4):325-332
Baclofen, the p-chlorophenyl analog of GABA, was found to exert antinociceptive activity and to induce catalepsy in mice. -Further pretreatment with sub-analgesic and sub cataleptic doses of baclofen was found to potentiate morphine-induced analgesia and catalepsy respectively. The possible mechanism involved in the induction of analgesia and catalepsy and in the potentiation of morphine-induced analgesia and catalepsy by baclofen is discussed on the basis of the inhibitory action of baclofen on the firing of the nigro-neostriatal dopaminergic neurons, which have been implicated in the control of nociceptive reflex activity and in the action of analgesic agents and whose hypofunctioning results in catalepsy.
[ABSTRACT]   Full text not available  [PDF]
  1,281 100 -
Distribution of chloramphenicol in blood and milk after oral administration in goat
BK Roy, NC Banerjee, SN Pandey
October-December 1982, 14(4):289-292
In goats, single dose oral administration of chloramphenicol did not produce therapeutic blood levels of the drug at 25mg and 50 mg/kg bw but at 100 mg and 200 mg/kg it produced therapeutic antimicrobial levels for 24 h and for more than 24 h, respectively. Single oral dose at 100 mg and 200 mg/kg gave therapeutic milk levels for 3 to 24 h and 1 h to 48 h, respectively. Both blood and milk were free from the drug at 72 h post administration after 100 and 200 mg/kg single oral doses. Species difference with regard to drug adsorptions from G. I. tract has been Suggested.
[ABSTRACT]   Full text not available  [PDF]
  1,247 85 -
Studies on autonomic actions of levamisole and phenylephrine in rat anococcygeus and frog’s isolated heart
DP Joshi, SC Verma
October-December 1982, 14(4):313-318
Levamisole. a broad spectrum anthelmintic and phenylephrine, an alpha-receptor stimulant, were studied on anococcygeus muscle of rat (RA) and isolated heart of frog. In RA, levamisole and phenylephrine both produces dose dependent contractions which were blocked by phentolamine, but not by practolol. a (-receptor blocker. Phenylephrine was more potent than levamisole in (-receptor stimulating activity. In isolated frog's heart, levamisole produced dose dependent negative inotropic effects. At higher doses it produced a complete cardiac arrest in diastole. The cardiac, inhibitory effects of levamisole are, not altered by atropine. Our results suggest that levamisole and phenylephrine both produces contractions in RA through stimulation of alpha-adrenoceptors. Inhibitory effects of levamisole on frog's cardiac muscles may be direct.
[ABSTRACT]   Full text not available  [PDF]
  1,145 126 -
Coagulation profile of indomethacin
BS Phadnaik, GC Parashar
October-December 1982, 14(4):355-356
The anti-inflammatory drug, Indomethacin. was found to have no significant effects on whole blood clotting time. one-stage prothrombin time, qualitative test for fibrinogen; visual thrombelastographic observations, fibrinolysis time, clot retraction time and bleeding time. The results indicate that the drug has no adverse effect on blood coagulation.
[ABSTRACT]   Full text not available  [PDF]
  1,157 106 -
Protective action in carbon-tetrachloride induced hepatotoxicity in dogs
GP Pandey, PN Shrivastava, HS Kushwah, IC Dutta
October-December 1982, 14(4):351-353
Efficacy of the indigenous drug, Livol (R), was studied on experimental hepatotoxicity in dogs caused by oral administration of carbon tetrachloride. A significant decline in elevated values of SGPT and prothrombin time indicated a protective action of Livol on the damaged liver tissue.
[ABSTRACT]   Full text not available  [PDF]
  1,135 111 -
In vitro hemolytic property of substituted phenothiazines
AK Khasnobis, J Saha, BP Mukherjee
October-December 1982, 14(4):305-308
In vitro hemolytic property of four commonly used substituted phenothiazine derivatives were studied on rabbit's washed erythrocytes, in isotonic saline. substitution of SCH2 group in place of H in position 2 of the phenothiazine ring, markedly increased the hemolytic activity, when compared with CF3 or Cl- substitution in the same position. Hemolytic property of these compounds also increased with the increase of incubation time and temperature.
[ABSTRACT]   Full text not available  [PDF]
  1,118 89 -
Modification of glibenclamide hypoglycaemia by some antihypertensive agents in rabbits
H Mishra, B Gupta, KK Saxena, VK Kulshreshtha, DN Prasad
October-December 1982, 14(4):301-304
Chlorthalidone (3.0 mg/kg), hydrochlorthiazide (3.0 mg/kg), frusemide (1.0 mg/kg) and clonidine (0.003 mg/kg) did not have any per se effect on fasting blood sugar level of rabbits upto 5 h. when clonidine was administered along with glibenclamide (0.025 mg/k), it not only caused an early onsent of hypo- glycaema but also produced greater fall in blood sugar than that observed with glibenclamide alone. The diuretics did not modify the hypoglycaemic activity of glibenclamide.
[ABSTRACT]   Full text not available  [PDF]
  1,084 104 -
Preliminary observation regarding the cataleptogenic activity of maprotiline in the mouse
JJ Balsara, VR Mane, VP Gada, NV Nandal, AG Chandorkar
October-December 1982, 14(4):345-350
Maprotiline (5-40 mg/kg ip) was found to induce catalepsy in mice. Treatment with apomorphine (2.5 and 5 mg/kg. ip) and atropine (20 mg/kg, ip) significantly reduced the cataleptic effect of maprotiline. Further, pretreatment with maprotiline (2.5-10 mg/kg, ip) significantly antagonised apomorphine-induced cage climbing behaviour in mice. The results suggest that the cataleptogenic effect of maprotiline is probably due to blockade of post-synaptic striatal dopamine receptors.
[ABSTRACT]   Full text not available  [PDF]
  1,056 90 -
Effect of Mk-212 on isolated guinea-pig heart
UP Patel, RK Goyal, SC Verma
October-December 1982, 14(4):319-323
MK-212 ; (6-Chloro-2-(1-piperazinyl)-pyrazine) (5x 10-8 to 4x10-7M) produced dose-dependent positive inotropic effects on guinea-pig heart. The responses to MK-212 were competitively blocked by mepyramine maleate and cyproheptadine. Metiamide did not alter the resonses to MK-212 on guinea-pig heart.The responses to MK-212 were also Inhibited competitively by propranolol. Reserpinization inhibited the responses to MK-212 completely. Our findings suggest that, MK-212 induced positive inotropic effect in guinea-pig heart 18 due to stimulation of post-syoaptic beta-receptors, involving the release of noradrenaline which follows the stimulation of either presynaptic serotonin or H1- histamine receptors.
[ABSTRACT]   Full text not available  [PDF]
  1,038 76 -
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