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1.
JAMC-Journal of Ayub Medical College-Abbotabad-Pakistan. 2008; 20 (2): 118-124
in English | IMEMR | ID: emr-87426

ABSTRACT

Opioid dependence is one of the major social and psychiatric problem of society. Unfortunately there is no non opiate treatment available. For centuries man has used plants for their healing proprieties. These plants play a fundamental part in all treatment modalities, both ancient and modern. This study was conducted to find non opiate treatment for opiate withdrawal. Total 35 known addicts of opiates were included in the study. This study was based on DSM IV criteria for opioid dependence. This study demonstrates that non opioid treatment for opioid addiction decreases the withdrawal effects significantly. It further demonstrates that there are no changes in physiological parameters of subjects during treatment [BP, Pulse rate etc.]. There is increased appetite but no significant weight gain in the subjects. Non opioid drug Nigella sativa is effective in long term treatment of opioid dependence. It not merely cures the opioid dependence but also cures the infections and weakness from which majority of addicts suffer


Subject(s)
Humans , Male , Nigella sativa , Phytotherapy , Treatment Outcome
2.
Pakistan Journal of Pharmacology. 2006; 23 (1): 51-60
in English | IMEMR | ID: emr-167425

ABSTRACT

Opioid dependence is one of the major social and psychiatric problem of society. Unfortunately there is no non-opiate treatment available. This study was conducted to find out the role of Nigella Sativa as a potential non-opiate treatment for opiate withdrawal. The study was conducted at the Department of Pharmacology, University of Karachi and Drug Rehabilitation Centre, R.H.C., Murad Memon Goth, Karachi. The study was based on DSM IV criteria for opioid dependence. Nigella Sativa 250 mg is found effective in long-term management of opioid dependence

3.
JAMC-Journal of Ayub Medical College-Abbotabad-Pakistan. 2006; 18 (3): 50-54
in English | IMEMR | ID: emr-77349

ABSTRACT

Administration of quinolone therapy is controversial during growing age as stated by earlier worker. The flroquinolones are currently not indicated for young children, because of arthropathy and adverse effect on growing cartilage shown by studies. However the effects of ciprofloxacin on epiphyseal growth plate has remained undocumented. This study is therefore, undertaken to determine the risk of ciprofloxacin administration an growing cartilage by prospective experimental animal study model using Wistar albino rat pups. Ciprofloxacin was administered to newly born Wistar albino rat pups with a doze of 20mg/kg body weight intraperitonealy twice a day from day-1 to day-14 after birth. The animals were sacrificed by deep ether anesthesia. The limbs were disarticulated from axial skeleton, soft tissue was removed. The intact bone mean length in millimeter of right and left humerus and femur was measured with the help of electronic vernier caliper and bones were fixed in 10% buffered farmalin. Decalcification was done in 10% nitric acid and 10% formic acid changes. After paraplast embeding, 4 mm thick longitudinal sections of the proximal long bones were cut by a rotary microtome. Routine staining with haemotoxylin and eosin was performed. Histomorphometry was done measuring the thickness of epiphyseal cartilage and was compared with similar value of control animals. The results were statistically analysed to find out the significance. The ciprofloxacin induces a mordanting effect as abviated by increased basophilia. Our study reveales that cirprofloxacin administration in the newly born pups decreased the width of epiphyseal growth plate cartilage by 10.43% in humerus and 4.72% in femur as compared to the growth of control cartilage. The decrease in the width was brought about mainly by the reduced count of the proliferative cells in the proliferative zone and the diminuation in the average size of the hypertrophic condryocytes in the hypertrophic zone. The reserve zone has become markedly reduced in thickness. The ciprofloxacin post-natal administration effected growth plate retardation by inhibiting the mitosis in the proliferative zone and also effected the mean length of humora and femora leading to reduction in limb length of rat pups


Subject(s)
Animals , Growth Plate/drug effects , Growth Plate/growth & development , Growth Plate/pathology , Cartilage/drug effects , Cartilage/growth & development , Osteogenesis/drug effects , Chondrocytes/drug effects , Rats
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