Abstract
Abstract Ketoprofen lysine salt (KL) is a new non- steroidal anti-inflammatory drug (NSAID) competing with ketoprofen (K) on the market. The former is believed to have gastroprotective properties and both to kill acute pain. In East Europe binge drinking and taking NSAIDs after is common. Some people use NSAIDs to treat the discomfort when they sober up. Vomiting after alcohol intoxication and gastritis after use of NSAIDs may produce malnutrition. The aim of the study was to compare nutritional status in female rats treated with KL or K after acute intoxication with ethyl alcohol. In this animal model we wanted to mimic human cases of NSAIDs use on the day(s) after binge drinking. The experiment was carried out on 36 female Wistar rats divided into 6 groups of 6: 1. treated with 50% etanol; 2. 0.9% NaCl; 3. 0.9% NaCl and K; 4. 50% etanol and K; 5. 0.9% NaCl and KL; 6. 50% etanol and KL. On day 7 animals were sacrificed. Their body, liver and kidney mass was recorded. The blood was obtained to measure blood morphology and biochemical parameters. K and alcohol in group 4 limited body mass gain (p<0.05 vs ethanol-group 1) and lowered albumin concentration (p<0.05 vs control-group 1). There was also a statistically significant decrease in the level of serum albumin of rats receiving KL (group 5) compared to the saline (group 2). K affects the nutritional status more than KLS after alcohol intoxication.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call