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   1993| April-June  | Volume 25 | Issue 2  
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Possible mechanism of antiinflammatory activity of Azadirachta indica leaf extract
RR Chattopadhyay, RN Chattopadhyay, SK Maitra
April-June 1993, 25(2):99-100
Effect of Azadirachta indica (A.indica) leaf extract on inflammatory oedema induced by chemical mediators (5-HT, histamine, bradykinin and PGE1) was studied to find out its possible mechanism of reported antiinflammatory effect against carrageenin induced rat hind paw oedema. The test material showed significant antiinflammatory effect against 5-HT and PGE1 induced inflammation but not on the inflammation induced by histamine and bradvkinin. Median effective doses of A.indica for 5-HT and PGE1 induced oedema were 1.17g and 930 mg/ kg respectively. The result suggests that A.indica extract's antiinflammatory effect may be due to antagonism of the deleterious effect of 5-HT and PGE1 on blood vessels.
[ABSTRACT]   Full text not available  [PDF]
  3,171 486 -
Felodipine in congestive heart failure - oxygen uptake, exercise capacity and echocardiographic evaluation
MU Rabbani, KC Singhal, M Ahmad, Husain Mubarak
April-June 1993, 25(2):110-111
The present study was undertaken to evaluate the role of felodipine, a newer calcium antagonist, in the management of congestive heart failure. Sixteen patients of congestive heart failure due to different causes received felodipine for 2 weeks. Ejection fraction, oxygen uptake and exercise capacity were evaluated after 2 weeks. Adverse reactions were noted. Felodipine therapy resulted in increased ejection fraction, oxygen uptake and exercise capacity. The drug was well tolerated. It is concluded that felodipine may be useful in the management of congestive heart failure.
[ABSTRACT]   Full text not available  [PDF]
  1,731 124 -
Drug enantiomers: Configuration and pharmacological implications
KD Tripathi
April-June 1993, 25(2):73-77
Full text not available  [PDF]
  1,427 313 -
Alterations in immediate and recent memory following acute oral and chronic inhalational exposure to methylparathion in rats
George Jennifer, Andrade Chittaranjan, Joseph Thangam
April-June 1993, 25(2):78-82
The effect of organophosphorous compounds on memory, both immediate and recent, were studied in the rat. Following acute oral or chronic inhalational exposure to methylparathion (MPT), rats were tested in a complex maze. Acute oral exposure was found to compromise recent memory function but not immediate memory function. After chronic inhalational exposure, no significant alterations in either recent or immediate memory functions were detected. The negative findings of this study may be genuine or may necessitate modifications in the memory task to more sensitively identify deficits. The modifications suggested are limitations of the maze-familiarization period, and use of a spaced-learning model instead of a massed-learning task model.
[ABSTRACT]   Full text not available  [PDF]
  1,596 115 -
5-Hydroxytryptamine receptor subtypes and antimigraine action
PR Saxena, WA Bax, MD Ferrari
April-June 1993, 25(2):60-67
The Nomenclature Committee of the Serotonin Club now recognizes four distinct types 5-hvdroxvtrvptamine (5-HT: serotonin) receptors called 5-HTI. 5-HT2. 5-HT3 and 5-HT4 . There is-now good evidence that the 5-HT1; and 5-HT2 receptors areheterogeneous and have several subtypes.Besides these receptors, there is another category of the so-called "orphan" receptors which await definitive classification. Two such kinds of receptors are collectively known as 5-HT1-like receptors; in order to distinguish between them they are sometimes denoted as 5-HT1X and 5-HT1Y, which mediate vasoconstriction (predominantly, but not exclusively, of cephalic vessels) and vasodilatation, respectively. Vasoconstriction in most other vessels is usually mediated by 5HT2A receptors. Injection of 5-HT and several other agonists at 5-HT1 -like receptors redistribute carotid blood flow so that arteriovenous anastomotic blood flow decreases despite, sometimes, an increase in tissue (arteriolar) blood Row. There is now good evidence that agonists at 'constrictor' 5HT1 -like (5-HT1x) receptors have the ability to abort migraine attacks. The other 5-HT receptors, including the 5-HT2A, 5-HT2c and 5-HT3 receptors, do not seem to play an important role in the antimigraine action of the currently available drugs.
[ABSTRACT]   Full text not available  [PDF]
  1,507 187 -
Evaluation of antihistaminic activity of septilin
S Shahani, VN Dhadkar, S Maroli
April-June 1993, 25(2):114-115
Full text not available  [PDF]
  1,388 172 -
Studies on diuretic effect of ST-93: A clonidine analog
R Kaushal, RM Tripathi, A Veeranjaneyulu, A Krishnamurthy, GS Thapar, RK Varma
April-June 1993, 25(2):95-98
ST-93 induced significant diuresis in rats. Dose-dependent effects were observed in urine volume and electrolyte excretion. Dose-related natriuretic and chloruretic activities were noticed. Prazosin and yohimbine significantly antagonised diuresis of ST- 93, while propranolol, cimetidine, cyproheptadine, naloxone and bicuculline had no such effect. The data suggest the possible involvement of both alpha-l and alpha-2 adrenoceptors in the diuretic effect of ST 93 in rats.
[ABSTRACT]   Full text not available  [PDF]
  1,402 108 -
Utilisation pattern of drugs in epilepsy and factors influencing reactions to commonly prescribed drugs - A study in South Indian patients
A Kuruvilla, S Prabakar
April-June 1993, 25(2):83-87
Drug utilisation pattern and incidence of reactions of commonly prescribed antiepileptic drugs in a group of patients are analysed. Incidence of reactions in this group is 27.4%. Most commonly prescribed drugs are phenobarbitone, phenytoin and carbamazepine. Number of drugs prescribed, age of patients and dose of drugs are the factors influencing the occurrence of reactions. Major reactions to phenobarbitone are related to central nervous system such as headache, drowsiness and giddiness. Gum hyperplasia is the commonest reaction reported by patients on phenytoin therapy. Cognltive functions are influenced by both phenobarbitone and phenytoin. Ataxia, nystagmus and slurred speech are the disturbing reactions caused by phenytoin.
[ABSTRACT]   Full text not available  [PDF]
  1,362 147 -
Effect of 7,8,9,10-tetrahydroazepino (2,l -b)-quinazoline-12 (6H), one, a new antiasthmatic compound on reproduction in rat and rabbit
GS Pahwa, U Zutshi
April-June 1993, 25(2):101-102
Reproductive studies of an antiasthmatic compound, 7,8,9-1 0- tetrahydroazepino (2,1 -b)-quinazoline- 12 (6H)-one were carried out as a prelude to clinical trials. Compound was devoid of any adverse effect on male and female fertility. There was no specific effect of treatment on gestation length. litter size and birth weight of pups in teratogenic studies in rats and rabbits. Prenatal and postnatal studies in rats revealed no untoward effect The compound seems to be free from any adverse effect on reproductive system
[ABSTRACT]   Full text not available  [PDF]
  1,306 156 -
Study of neuromuscular blockade following high dose chandonium iodide
YV Suri, PC Tripathi, SPS Gaur, RC Srimal, BN Dhawan
April-June 1993, 25(2):91-94
High dose chandonium iodide, 200, 250,300,350 and 400 'g/kg was randomly administered to 45 ASA physical status I-II patients for muscle relaxation during general and gynaecological surgery. Neuromuscular blockade was quantitated with ulnar nerve stimulation (myotest) and also assessed clinically. Time to onset of muscle relaxation, apnoea, endotracheal intubation conditions, duration of neuromuscular blockade, and haemodynamic effects of chandonium at each dose were evaluated and compared. Time to onset of muscular relaxation decreased from 72.3(15.5 to 38.0 15.3 second as the chandonium dose was increased from 200 to 400 'g/kg (P< 0.01). Recovery of limb movements and hand grip after extubation was not altered clinically or statistically. However, increased recovery time to head lift for 5 seconds from 12.7 9.6 to 20.1 11.2 min was seen with higher dosage of chandonium. No significant haemodynamic differences between 250 and 400 'g/kg groups were observed. High doses of chandonium, may, therefore, be a useful alternative to succinylcholine to achieve similar quantitative as well as qualitative neuromuscular blockade for intubation conditions.
[ABSTRACT]   Full text not available  [PDF]
  1,360 86 -
Effect of oral administration of abana, an ayurvedic formulation on experimental cardiac arrhythmias
CS Gautam, P Pandhi, PL Sharma
April-June 1993, 25(2):105-106
Abana, an ayurvedic formulation was studied in dogs (n=l9) for its anti-arrhythmic activity. After prophylactic oral administration it produced slight reduction in the duration of aconitine induced atrial flutter/fibrillation but no effect was observed on atrial/ventricular rates, Curative effect was not seen against coronary artery ligation induced ventricular tachycardia.
[ABSTRACT]   Full text not available  [PDF]
  1,312 128 -
Clinical trial of nifedipine in primary dysmenorrhoea
S Kulshreshtha, P Sharma, AL Sharma, S Agrawal
April-June 1993, 25(2):88-90
Fifty unmarried girls suffering with primary dysmenorrhoea, participated in a double-blind, parallel trial of nifedipine versus placebo. The efficacy of the nifedipine/placebo was assessed by measuring the intensity of pain, the degree of pain relief, the necessity of a supplementary analgesic and the extent to which drugs enable the patients to continue their daily activities during each dysmenorrhoeic cycle. In this study nifedipine was found to be significantly superior as compared to the placebo. Among severely incapacitated group more number of nifedipine treated patients(11 /1 6) were able to continue their daily activities as compared to placebo group (4/13). Only 3 girls experienced few side effects.
[ABSTRACT]   Full text not available  [PDF]
  1,277 106 -
Duration of the neuromuscular blocking action of antidepressants
BG Patel, NP Chotai
April-June 1993, 25(2):107-109
After 15 days of single daily oral administration of tricyclic antidepressants (imipramine, desipramine 10 mg/kg each, amitriptyline, nortriptyline 7.5 mg/kg each and protriptyline 5 mgikg) in rabbits, reduced the minimum effective dose of gallamine to elicit head drop. Potentiating effect persisted significantly up to 24 hour. Similarly double the doses of these tricyclic antidepressants reduced the quantity of gallamine significantly up to 48 h. and total recovery from the effect appeared after 72 h. It is suggested that the potentiation of the action of gallamine by tricyclic antidepressants may be of clinical importance in patients especially if any of these tricyclic antidepressants has been taken shortly before.
[ABSTRACT]   Full text not available  [PDF]
  1,275 102 -
Poor patient compliance to prescribed doses of insulin in Zambian patients
AK Khare
April-June 1993, 25(2):112-113
Patients compliance to insulin was investigated in 45 Zambian diabetic patients. Non-compliance was found in 31 of them. 25 patients were underdosing while 6 were overdosing themselves. The major reasons for it were inability to understand the usage of syringes due to freauent changes in insulin strenaths and type of syringes; and deliberate underdosing for fear of interrupted in supply.
[ABSTRACT]   Full text not available  [PDF]
  1,245 100 -
Dose related increase in the serum levels of protein bound hexose after acute exposure with cadmium in rats:
AB Patel, Bhatt H Venkatakrishna
April-June 1993, 25(2):103-104
The rats were challenged with 0.5, 1, 2 or 3 mg/kg cadmium (i.p) to observe its effect on the serum levels of protein bound hexose (PBH). Dose dependent increase was found in the levels of PBH, 48 hrs post cadmium administration. Serum levels of PBH might be useful for monitoring the cadmium toxicity with known cadmium exposure.
[ABSTRACT]   Full text not available  [PDF]
  1,205 91 -
A critical examination of marketing of pharmaceuticals
A Chetley, B Mintzes
April-June 1993, 25(2):116-116
Full text not available  [PDF]
  1,123 98 -
The protective role of amiloride and its analogs in ischemia/reperfusion challenge
Massaeli Hamid, GN Pierce
April-June 1993, 25(2):68-72
Full text not available  [PDF]
  978 99 -
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