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1.
Health [The]. 2011; 2 (2): 37-40
in English | IMEMR | ID: emr-191885

ABSTRACT

Background: Children of commercial sex workers [CSW] are deprived from almost all the rights of the society. More attention is paid to the CSWs but their children are neglected. This study was conducted to estimate the morbidity and psychosocial behaviour of children of CSWs and their needs. Methods: A community-based cross-sectional study was conducted. Results: Among 152 children, 72% were malnourished. Exclusive breast feeding [EBF] practices were poor. Only 47% were immunized and health status was not at par with national averages. The high prevalence of cerebral palsy may reflect poor antenatal, perinatal and essential new born care. The most popular desired profession was teacher [20%] followed by player, doctor, and artist. 7% wanted to become soldier while 8% felt very bad about themselves and 10.5% could not sleep well at night. Conclusion: The indirectly elucidated needs regarding health and behaviour of the children of CSWs are only the tip of the iceberg. The children need formal and non-formal health and life skill education and the caregivers need behavioural change communication on health and hygiene

2.
Biomedical and Environmental Sciences ; (12): 56-63, 2007.
Article in English | WPRIM | ID: wpr-249887

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of pre-treatment of alpha-ketoglutarate (alpha-KG) on cyanide-induced lethality and changes in various physiological parameters in rodents.</p><p><b>METHODS</b>The LD50 of potassium cyanide (KCN) given orally (po), intraperitoneally (ip), subcutaneously (sc) or intravenously (iv) was determined in male mice, in the presence or absence alpha-KG given po, ip or iv. alpha-KG was administered 10, 20 or 40 min prior to KCN at 0.50, 1.0 or 2.0 g/kg by po or ip route, and at 0.10, 0.20 or 0.40 g/kg by iv route. Protection index (PI) was calculated as the ratio of LD50 of KCN in the presence of alpha-KG (protected animals) and LD50 of KCN in the absence of alpha-KG (unprotected animals). In a separate experiment, several physiological variables viz. mean arterial pressure (MAP), heart rate (HR), respiratory rate (RR), neuromuscular transmission (NMT) and rectal temperature (RT) were measured in anesthetized female rats pre-treated (-10 min) with po (2.0 g/kg) or iv (0.125 g/kg) alpha-KG and then administered sub-lethal (0.75 LD50) or lethal (2.0, 4.0 or 8.0 LD50) doses of KCN (po).</p><p><b>RESULTS</b>PI of 4.52, 6.40 and 7.60 at -10 min, 3.20, 5.40 and 6.40 at -20 min, and 1.40, 3.20 and 5.40 at -40 min of po administration with a-KG was observed for 0.50, 1.0 and 2.0 g/kg doses, respectively, against KCN given by po route. When KCN was given ip, a PI of 3.38, 4.79 and 5.70 was observed for 0.50, 1.0 and 2.0 g/kg alpha-KG given ip (-10 min), respectively. A lower PI of 3.37, 2.83 and 2.38 was observed when KCN given sc was challenged by 2.0 g/kg alpha-KG given ip at -10, -20 or -40 min, respectively. Similarly, a PI of 3.37, 2.83 and 2.0 was noted when KCN given sc was antagonized by 2.0 g/kg alpha-KG given po at -10, -20 or -40 min, respectively. No appreciable protection was observed when lower doses of alpha-KG (ip or po) challenged KCN given by sc route. Pre-treatment of iv or po administration of alpha-KG did not afford any protection against KCN given po or iv route. Oral treatment of 0.75 LD50 KCN caused significant decrease in MAP and HR after 15 min, RR after 30 min and NMT after 60 min. There was no effect on RT. No reduction in MAP, HR, RR and RT was observed when rats received 2.0 or 4.0 LD50 KCN after pre-treatment of alpha-KG (po; 2.0 g/kg). However, no protection was observed on NMT. Protective efficacy of alpha-KG was not observed on MAP, HR, RR, and NMT decreased by 8.0 LD50 KCN. Decrease in MAP and NMT caused by 2.0 LD50 KCN (po) was resolved by iv administration of alpha-KG.</p><p><b>CONCLUSIONS</b>Cyanide antagonism by alpha-KG is best exhibited when both alpha-KG and KCN are given by po route. The protective effect of a-KG on cyanide-induced changes in several physiological parameters also indicates a promising role of alpha-KG as an alternative cyanide antidote.</p>


Subject(s)
Animals , Female , Male , Mice , Rats , Administration, Oral , Antidotes , Dose-Response Relationship, Drug , Injections, Intraperitoneal , Injections, Intravenous , Injections, Subcutaneous , Ketoglutaric Acids , Lethal Dose 50 , Potassium Cyanide , Poisoning , Rats, Wistar
3.
Biomedical and Environmental Sciences ; (12): 61-66, 2006.
Article in English | WPRIM | ID: wpr-229724

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the biochemical changes in rat brain and liver following acute exposure to a lethal dose of cyanide, and its response to treatment of alpha-ketoglutarate (alpha-KG) in the absence or presence of sodium thiosulfate (STS).</p><p><b>METHODS</b>Female rats were administered 2.0 LD50 potassium cyanide (KCN; oral) in the absence or presence of pre-treatment (-10 min), simultaneous treatment (0 min) or post-treatment (+2-3 min) of alpha-KG (2.0 g/kg, oral) and/or STS (1.0 g/kg, intraperitoneal, -15 min, 0 min or + 2-3 min). At the time of onset of signs and symptoms of KCN toxicity (2-4 min) and at the time of death (5-15 min), various parameters particularly akin to oxidative stress viz. cytochrome oxidase (CYTOX), superoxide dismutase (SOD), glutathione peroxidase (GPx), reduced glutathione (GSH) and oxidized glutathione (GSSG) in brain, and CYTOX, sorbitol dehydrogenase (SDH), alkaline phosphatase (ALP), GSH and GSSG in liver homogenate were measured.</p><p><b>RESULTS</b>At both time intervals brain CYTOX, SOD, GPx, and GSH significantly reduced (percent inhibition compared to control) to 24%, 56%, 77%, and 65%, and 44%, 46%, 78%, and 57%, respectively. At the corresponding time points liver CYTOX and GSH reduced to 74% and 63%, and 44% and 68%, respectively. The levels of GSSG in the brain and liver, and hepatic ALP and SDH were unchanged. Pre-treatment and simultaneous treatment of a-KG alone or with STS conferred significant protection on above variables. Post-treatment was effective in restoring the changes in liver but failed to normalize the changes in the brain.</p><p><b>CONCLUSIONS</b>Oral treatment with alpha-KG alone or in combination with STS has protective effects on cyanide-induced biochemical alterations in rat brain and liver.</p>


Subject(s)
Animals , Female , Rats , Antidotes , Pharmacology , Brain , Metabolism , Electron Transport Complex IV , Metabolism , Glutathione Peroxidase , Metabolism , Glutathione Reductase , Metabolism , Ketoglutaric Acids , Pharmacology , Liver , Metabolism , Oxidative Stress , Poisoning , Potassium Cyanide , Poisoning , Rats, Wistar , Superoxide Dismutase , Metabolism , Thiosulfates , Pharmacology
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