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Biomedical subjects

S Qureshi

Publications and source records attributed to S Qureshi.

At least 73 records · Page 4Linked to original sources
PubMed1992

Toxicity studies on Alpinia galanga and Curcuma longa.

Acute (24 h) and chronic (90 days) oral toxicity studies on the ethanolic extracts of the rhizomes of Alpinia galanga and Curcuma longa were carried out in mice. Acute dosages were 0.5, 1.0, and 3 g/kg body weight while the chronic dosage was 100 mg/kg/day as the extract. All external morphological, hematological, and spermatogenic changes, in addition to body weight and vital organ weights were recorded. During this investigation no significant mortality as compared to the controls was observed. The weight gain in the A. galanga treated animals was significant as in the control group while the C. longa-treated animals gained no significant weight after chronic treatment. C. longa treatment induced significant changes in heart and lungs weights upon chronic treatment. Hematological studies revealed a significant rise in the RBC level of A. galanga-treated animals and a significant fall in the WBC and RBC levels of the C. longa-treated animals as compared to the controls. The gain in weights of sexual organs and increased sperm motility and sperm counts were observed in both groups of extract-treated male mice, however, these changes were highly significant in the A. galanga-treated group. Both extracts failed to show any spermatotoxic effects.

Animals↗
PubMed1991

Uric acid as an inhibitor of cyclophosphamide-induced micronuclei in mice.

Swiss albino male mice, 6-8 weeks old, were treated orally with different doses of uric acid dissolved in water for 7 days. Some of the mice in each group were injected i.p. with cyclophosphamide (25 mg/kg) and killed after 30 h. The blood of all animals was analyzed for uric acid levels. The femoral cells of the mice in different groups were collected and studied. Uric acid was found to be devoid of mitodepressant or clastogenic activity at 10-100 mg/kg/day. Pretreatment with uric acid was found to provide significant protection against cyclophosphamide-induced bone marrow depression and micronucleated polychromatic erythrocytes.

Animals↗
PubMed1991

Absence of one atrioventricular connexion--a terminologic problem.

We present a patient in whom the heart was right-sided, with usual atrial position, absence of the right-sided atrioventricular connexion, and a single outlet via the aorta from a dominant morphologically right ventricle. We use the case to illustrate potential problems in the terminology as used to describe the absence of one atrioventricular connexion. Our case shows why absence of one atrioventricular connexion must be classified according to the side of the missing connexion, and not the anatomy of the atrial or ventricular chambers involved. To simplify the approach to certain hearts, the use of the concept of one concordant or discordant atrioventricular connexion may be justified when the other atrioventricular connexion is absent.

Female↗
PubMed1991

Uric acid as an inhibitor of biochemical changes induced by cyclophosphamide in mice.

The biochemical changes induced by uric acid, cyclophosphamide and uric acid plus cyclophosphamide were evaluated in Swiss albino male mice. Uric acid dissolved in water was administered orally in different doses for 7 days. Some mice from each group were injected intraperitoneally with cyclophosphamide (25 mg/kg) and sacrificed after 30 h. The blood of all animals was analyzed for uric acid levels. Uric acid was found not to affect the biosynthesis of nucleic acids and proteins in liver, testes and brain at 10-100 mg/kg/d. Pretreatment with uric acid provided significant protection against cyclophosphamide-induced impairment of DNA, RNA and protein biosynthesis.

Animals↗
PubMed1991

Toxicity studies in mice of ethanol extracts of Foeniculum vulgare fruit and Ruta chalepensis aerial parts.

Acute (24-h) and chronic (90-day) oral toxicity studies on the ethanolic extracts of Foeniculum vulgare fruit and Ruta chalepensis aerial parts were carried out in mice. Acute dosages were 0.5, 1.0 and 3 g/kg while the chronic dosage was 100 mg/kg per day of extract. All external morphological, haematological and spermatogenic changes, in addition to body and vital organ weights were recorded. The extracts caused no significant acute or chronic mortality as compared to controls during this investigation. The treated male mice gained significant weight during chronic treatment while a loss or no significant change in weight was noticed in the female mice treated with the same extracts. Haematological studies revealed a significant fall in RBC level of R. chalepensis-treated animals. Both the extracts failed to show spermatotoxic effects.

Animals↗
PubMed1991

Mitodepressive, clastogenic and biochemical effects of (+)-usnic acid in mice.

Mice were treated orally with aqueous suspensions of (+)-usnic acid in a single dose of either 100 or 200 mg/kg. The effects on femur cells and proteins and on nucleic acids of liver cells were studied 24-72 h after treatment. (+)-Usnic acid was found to affect the proliferation of polychromatic erythrocytes possibly by interference with RNA biosynthesis. The slight increase in the micronucleated polychromatic erythrocytes without affecting DNA synthesis suggests an effect of usnic acid on spindle apparatus.

Administration, Oral↗
PubMed1991

The toxicity of Catha edulis (khat) in mice.

A large number of people in East Africa and Southern Arabia chew khat leaves because of its pleasurable and stimulating effects. Due to its habit forming property, the khat has been classified as a "Substance of Abuse" by the World Health Organization. In view of the large number of medical problems reported in khat chewers, the present study was undertaken to investigate the chronic toxicity of khat in mice. Three groups of mice were treated with aqueous solution of khat extract in the dose of 50, 100, and 200 mg/kg. body weight daily by oral intubation route for 6 weeks. The results indicated a dose-dependent decrease in body weight, an increase in the incidence of mortality and induction of site specific body and eye lesions. The histopathological examination of the lesions revealed reactive hyperplasia and necrosis in the lymphoid tissues. The necrotic areas in the subcutaneous tissues showed the presence of numerous polymorphs.

Animals↗
PubMed1991

Toxicological studies of Melia azedarach L. (flowers and berries).

Toxicological evaluation of Media azedarach Linn. was carried out in lower laboratory animals, i.e. rats and mice by oral and intravenous routes. Aqueous and alcoholic extracts were found to be non-toxic uptil a dose of 1500 mg/kg orally in mice and rats. When injected aqueous extract intravenously, LD50 was 395, 580 mg/kg (flowers) and 700, 925 mg/kg (berries) respectively in mice and rats. It was also observed that alcoholic and aqueous extracts of Melia azedarach have a mild CNS sedative effect.

Journal Article↗
PubMed1990

The induction of dominant lethal mutations upon chronic administration of khat (Catha edulis) in albino mice.

The mutagenicity of a methanolic extract of khat has been evaluated on male germ cells using the dominant lethal test in albino mice. An aqueous solution of khat extract was administered orally in doses of 50, 100 and 200 mg/kg body wt., respectively, to 3 different groups of male mice for a period of 6 weeks. At the end of treatment each male mouse was allowed to mate with 2 different groups of 3 females each, on 2 consecutive weeks. These females were necropsied on the 13th day of their presumptive mating, and the number of implants in each female and the ratio of live and dead embryos were determined. The results of this study showed that the treatment of male mice over a period of 6 weeks produced a dose-dependent reduction in the rate of fertility in the first week after mating, which was irreversible in the second week at the highest dose (200 mg/kg). Khat extract also induced post-implantation loss during the first week following treatment. However, a comparison of the results of the first and second weeks showed a reversible pattern of dominant lethality.

Animals↗
PubMed1990

Preliminary toxicity studies on ethanol extracts of the aerial parts of Artemisia abyssinica and A. Inculta in mice.

Ethanolic extracts of the aerial parts of Artemisia abyssinica and A. inculta were subjected to acute toxicity observations in mice for 24 h and chronic toxicity evaluation for 3 months. External morphological changes, visceral toxicity, haematological changes, spermatogenic dysfunction and effect on body weight and vital organ weight were recorded. In both the chronically treated groups, no significant acute mortality was observed up to 3 g/kg p.o. There was no weight gain in A. abyssinica chronically-treated mice while the weight gain of A. inculta-treated animals matched that of the control group. Significant sperm damage was observed in A. abyssinica-treated mice while A. inculta failed to produce any significant spermatotoxic effect.

Alopecia↗
PubMed1990

Effect of Allium sativum on epididymal spermatozoa, estradiol-treated mice and general toxicity.

A water extract of Allium sativum (garlic) was given to male and female mice in drinking water (100 mg/kg/day) for three months. There was a significant increase in the weight of seminal vesicles and epididymides of male animals as compared to controls and the sperm count was significantly elevated. There was no increase in the body weight of the test animals, and weights of heart, liver and spleen were reduced as compared to controls. Haematological studies revealed an increase in WBC and a decrease in RBC levels of the test animals. Three-day intraperitonial treatment (500 mg/kg) with the A. sativum extract failed to exhibit any estrogenic or antiestrogenic activity.

Allium↗
PubMed1990

Embolisation of a complex coronary arteriovenous fistula in a 6 year old child: the need for specialised embolisation techniques.

Transcatheter embolisation was performed in a six year old child with a large haemodynamically significant arteriovenous fistula between the left coronary artery and right ventricle. The fistula seemed to fill via a single large septal branch of the left anterior descending coronary artery. This was occluded distally with a detachable balloon backed up by a proximal coil. After this the flow through the fistula was considerably reduced but it still filled via a small diagonal branch that had not been noted previously. This branch was subsequently occluded in its most distal part by a coaxial catheter technique and a single microcoil. Complete occlusion of the fistula was produced and there were no complications.

Arteriovenous Malformations↗