iver is the main organ in the body for intense metabolism and excretion. A large number of chemicals and medicines/drugs used routinely in daily lives can cause disorders and possibly liver disease. The aim of exploring some aspects related to the potential hepatoprotective activity of Ganoderma lucidum versus carbon tetrachloride (CCl4) intoxication in rat liver. When compared with the normal group rats, the CCl4 treated rats showed significant (p≤0.05) decreased in different biological parameters. Also, biochemical parameters such liver enzymes activities were significant (p≤0.05) elevation when compared with the normal group rats. For immunological parameters, Alb was significant (p≤0.05) decreased by the rate of -29.44 and TNF-α increased by 93.28%. This also coincided with an imbalance in the oxidants/antioxidants status in the blood, which was represented by a decrease in the level of antioxidants and a high level of oxidants. All of those parameters were indicating the liver injury by CCl4. Whereas animal treated/fed with Ganoderma lucidum powder (GLP) showed significant (p≤0.05) improvements in all previous status biomarkers indicating the protection against hepatic cell damage. A positive dose -response was recorded between the concentrations of GLP applied and the level of improvement noticed in all measured markers. In conclusion, GLP was effective in protecting against CCl4-induced liver disorders. Present study recommended like of that algae powder by a concentrations up to 5% (w/w), amount to be included in daily diets, drinks and food supplementation after trial study on volunteer human.
Chemotherapeutic agent, busulfan, induce oxidative stress as a mechanism to kill cancer cells, however, it may also cause oxidative stress in non-target tissues and thereby lead to normal tissue injury. Milk thistle (Silybum marianum L.) has been used for centuries as a herbal drug. The present study was carried out to investigate the potential effects of wild Silybum marianum seed ethanol extract (SMSEE) intervention on oxidative stress induced by busulfan drug in different organs of Rats. For the study 42 rats were prepared and fed with special ration, then they were divided to 7 groups with 6 rats in each group: group 1, Normal control: healthy rats without intervention; group 2.control SMSEE, 400 mg/kg/day SMSEE; group 3, positive control group received 20 mg/kg/day busulfan, group 4, treated group received 20 mg/kg/day busulfan + 200 mg/kg/day SMSEE; group 5, treated group received 20 mg/kg/day busulfan+ 400 mg/kg/day SMSEE; group 6, treated group received 20 mg/kg/day busulfan + 600 mg/kg/day SMSEE; group 7, treated group received 20 mg/kg/day busulfan + 800 mg/kg/day SMSEE. The amount of oxidative stress parameters (ROS and MDA), glutathione fractions (GSH and GSSG), and antioxidant enzymes (GSH-Px, GSH-Rd, SOD and CAT) in the different tissue extracts (liver, kidneys, heart, spleen, pancreas and testes) were measured. The results of this study showed that after busulfan treatment the levels of ROS and MDA were significantly (p≤0.05) increased and GSH, GSSG, GSH-Px, GSH-Rd, SOD and CAT were decreased in all studied organs. Treatment of busulfan administration rats with SMSEE leads to the opposite direction by different rates. In conclusion, the use of busulfan in rats administration induce oxidative stress in different organs and SMSEE had an preventive role through decreasing the ROS and the lipid peroxidation, and improvement the oxidative defense system. These results provide a basis for the use of Silybum marianum extracts as promising tools in the future for many important nutritional and therapeutic applications.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.