M. KurÅat, Ö. Yılmaz, I. Emre, Å. Civelek, Z. Gökçe
{"title":"Some Biological Contents and Radical Scavenging Activities of Five Artemisia L. Species Growing in Turkey","authors":"M. KurÅat, Ö. Yılmaz, I. Emre, Å. Civelek, Z. Gökçe","doi":"10.4172/2157-7609.1000172","DOIUrl":"https://doi.org/10.4172/2157-7609.1000172","url":null,"abstract":"In the present study, fatty acid compositions, vitamin and sterol contents, flavonoid constituents and radical scavenging activity of extracts of the Artemisia species from Turkey (A. absinthium L., A. vulgaris L., A. austriaca Jacq., A. verlotiorum Lamotte and A. caucasica Willd.) are studied. Results of present study demonstrated that the main fatty acids in the extracts of Artemisia L. are determined as palmitic acid (C16:0; 7.1-25.9%), stearic acid (C18:0; 2.6-12.5%), palmitoleic acid (C16:1 n9; 1.3-13.1%), oleic acid (C18:1 n9; 1.5-20.3%), linoleic acid (C18:2 n6; 14.1-63.4%), docosadienoic acid (C22:2; 1.6-10.3%). Lipide-soluble vitamin contents of Artemisia L. species are found low concentrations. Also, it is determined that A. absinthium and A. vulgaris have rich in term of ergosterol content. Furthermore, it is showed that Artemisia L. species studied rich in flavonoid content apart from A. vulgaris. It is determined that quercetin and kaempferol contents of Artemisia L. species are low. In addition, it is observed that the studied Artemisia L. species posses strong DPPH radical scavenging activity.","PeriodicalId":15537,"journal":{"name":"Journal of Drug Metabolism and Toxicology","volume":"57 1","pages":"1-5"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80772982","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Efficacy Study of Livartho against Paracetamol Induced Hepatotoxicity in Adult Sprague Dawley Rats","authors":"V. Dwivedi, J. Mishra, A. Shrivastava","doi":"10.4172/2157-7609.1000175","DOIUrl":"https://doi.org/10.4172/2157-7609.1000175","url":null,"abstract":"Liver disease is a worldwide problem. It is an exposed to many kinds of xenobiotics and therapeutic agents. The purpose of this study was to evaluate therapeutic effect of Livartho drug in paracetamol induced hepatic damage Sprague dawley rats. Paracetamol at the dose level of 900mg/kg body weight administered through intraperitoneal route once daily for one week to produced liver damage in rats as manifested by the significantly decrease body weight and feed consumption along with significantly increase liver organ weight and serum levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), lactate dehydrogenase (LDH), total bilirubin, cholesterol and triglyceride and decrease the total protein and albumin levels along with significantly increase myloperoxidase enzyme activity, lipid peroxidation and protein carbonyl levels as compared to control group. The antioxidant parameters such as reduced glutathione (GSH), oxidized glutathione (GSSG), total thiol and GSH/ GSSG ratio were also found lowered in paracetamol treated group as compared with control. After treatment with Livartho drug (206.6 mg/kg body weight) once daily for 16 days to paracetamol treated rats shows significantly lowered the afore mentioned biochemical parameter whereas protein and albumin levels were increased along with significant increased above mentioned antioxidant enzymatic parameters. The results of this study strongly indicate that Livartho drug is most effective medicine which has potent hepatoprotective action and free radical scavenger against paracetamol induced hepatic damage in Sprague dawley rats.","PeriodicalId":15537,"journal":{"name":"Journal of Drug Metabolism and Toxicology","volume":"1 1","pages":"1-7"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74895004","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"The Role of Biotransformation in Drug Discovery and Development","authors":"Selamu Kebamo, Shibiru Tesema, Bekesho Geleta","doi":"10.4172/2157-7609.1000196","DOIUrl":"https://doi.org/10.4172/2157-7609.1000196","url":null,"abstract":"Biotransformation is a process by which organic compounds are transformed from one form to another, aided by organisms such as bacteria, fungi and enzymes. It plays a major role and determines the fate of the prospective drugs. Biotransformation must take place only after the drugs reach their specific target site and produce the desired effects. In addition, the nature of the metabolites produced from the drug, must be thoroughly studied; otherwise, the drugs would be rejected during the screening process. Hence, drug metabolism is a major criterion in the highthroughput screening of prospective drugs. \u0000Biotransformation has an important role in the determination of the pharmacokinetic parameters like oral bioavailability, drug-drug interaction, clearance and the half-life of the entity within the cell. It is very essential in the toxicity studies too. Biotransformation is used as a valuable strategy to build molecules, similar to parent drug in the drug discovery programme. It can play an important role in identifying factors underlying the problems, facilitate the optimal selection of compounds for further development, provide information on metabolites for possible improvement in drug design, and contribute to the identification of the appropriate animal species for subsequent toxicity testing. Hence, so","PeriodicalId":15537,"journal":{"name":"Journal of Drug Metabolism and Toxicology","volume":"142 1","pages":"1-13"},"PeriodicalIF":0.0,"publicationDate":"2015-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80176294","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
H. Fahmy, F. F. Mohammed, Radwa T Abdelrahman, M. A. Elfetoh, Yomna A Mohammed
{"title":"Effect of Radiofrequency Waves Emitted From Conventional WIFI Devices on Some Oxidative Stress Parameters in Rat Kidney","authors":"H. Fahmy, F. F. Mohammed, Radwa T Abdelrahman, M. A. Elfetoh, Yomna A Mohammed","doi":"10.4172/2157-7609.1000195","DOIUrl":"https://doi.org/10.4172/2157-7609.1000195","url":null,"abstract":"Wireless Fidelity (WIFI) is widely used in cell phones, computers and electronic devices to access the Internet. It is unclear whether or not the frequency range of the WIFI has any harmful biological effects. In this report, the effect of standard 2.45 GHz radio frequency source (Averaged whole body specific absorption rate (SAR) 0.01 W/ Kg, 24 hours daily for 40 successive days) on some oxidative stress parameters was examined in Wistar female rats. We found that exposure to WIFI decreased the malondialdehyde levels as well as the glutathione-S-transferase and catalase activities. Moreover, the activity of superoxide dismutase showed significant increase in the WIFIexposed group relative to the control group. Meanwhile, kidney functions were found to be unaffected. In addition, no significant histological alterations in rats’ kidneys were detected in WIFI-exposed group. These results indicate that WIFI exposure used in the present study implies oxidative alterations in rat kidneys, which does not result in severe consequences due to the effective activity of the antioxidant enzyme system of the rat kidneys.","PeriodicalId":15537,"journal":{"name":"Journal of Drug Metabolism and Toxicology","volume":"72 1","pages":"1-6"},"PeriodicalIF":0.0,"publicationDate":"2015-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90365809","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Chronotherapeutic Drug Delivery Systems","authors":"iyan Shanmugan, B. Ramu, Ameedi","doi":"10.4172/2157-7609.1000194","DOIUrl":"https://doi.org/10.4172/2157-7609.1000194","url":null,"abstract":"Recent advances in chronotherapeutics led to the development of pulsatile drug delivery systems which effectively delivered the drug at specified time. Diseases like asthma, arthritis, cancer, diabetes, hypertension, ulcer, hypercholesterolemia, congestive heart failure, stroke etc. show different day night pattern in onset and symptoms exacerbation. Pulsatile drug delivery systems deliver the drug at right time in desired levels providing the multiple benefits over the conventional dosage forms. According to the circadian rhythms of the body drug is facilitated to completely release after a lag time especially for drugs eliciting higher first pass effect and where nocturnal dosing is required these systems are highly beneficial. This review epitomizes the special focus on chronotherapeutics, various approaches in chronotherapeutic drug delivery and applications.","PeriodicalId":15537,"journal":{"name":"Journal of Drug Metabolism and Toxicology","volume":"6 1","pages":"1-7"},"PeriodicalIF":0.0,"publicationDate":"2015-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86908898","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
P. Praveen, S. Ganguly, R. Wakchaure, P. A. Para, S. Shekhar, N. Dalai
{"title":"Tuberculosis, a Milk-Borne Zoonosis: A Critical Review","authors":"P. Praveen, S. Ganguly, R. Wakchaure, P. A. Para, S. Shekhar, N. Dalai","doi":"10.4172/2157-7609.1000E126","DOIUrl":"https://doi.org/10.4172/2157-7609.1000E126","url":null,"abstract":"Tuberculosis is a widespread infectious disease caused by Mycobacterium tuberculosis. Tuberculosis attacks on lungs but also affects the other parts of the body. It is spread through the air when people who have an active Tuberculosis infection cough, sneeze, or otherwise transmit respiratory fluids through the air. Most infections do not have symptoms, known as latent tuberculosis. About one in ten latent infections eventually progresses to active disease which if left untreated kills more than 50% of those so infected. One-third of the world’s population is thought to have been infected with M. tuberculosis and new infections occur in about 1% of the population each year.","PeriodicalId":15537,"journal":{"name":"Journal of Drug Metabolism and Toxicology","volume":"16 1","pages":"1-2"},"PeriodicalIF":0.0,"publicationDate":"2015-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76183868","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Toxicological Evaluation of Gum (Galactomannans) Isolated from Senna tora Seeds","authors":"H. Pawar, K. Lalitha","doi":"10.4172/2157-7609.1000193","DOIUrl":"https://doi.org/10.4172/2157-7609.1000193","url":null,"abstract":"Seed gums possess excellent emulsifying, suspending, binding, thickening stabilizing and water-holding properties. Therefore they are used in various pharmaceutical dosage forms like tablets, syrups, suspensions, lotions, ointments and for sustained drug release systems. Gum derived from the seeds of Senna tora L. is common herbaceous annual occurring weed throughout the India. The present investigation reports preliminary phytochemical screening and toxicological evaluation of the isolated seed gum from the Senna tora. The acute toxicity study was carried out in adult albino rats by “fixed dose” method. The sub-acute toxicity study was carried out for 28 days in wistar albino rats. All the Animals used were observed for clinical signs, physical abnormalities, changes in body weight and pre-terminal deaths. Laboratory investigations such as hematology and clinical chemistry were performed at sacrifice and the data were statistically analyzed. Based on the results of the acute oral toxicity on the polysaccharide in Wistar rats, it may be concluded that the LD50 of the Senna tora gum is greater than 2000 mg/kg. In the sub-acute toxicity study, the gum treated groups did not show any sign of toxicity after getting treated at dose levels of 500, 1000 and 1500 mg/kg daily for 28 days.","PeriodicalId":15537,"journal":{"name":"Journal of Drug Metabolism and Toxicology","volume":"17 1","pages":"1-5"},"PeriodicalIF":0.0,"publicationDate":"2015-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88029147","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
R. Wakchaure, S. Ganguly, P. Praveen, Avinash Kumar, Subhash Sharma, T. Mahajan
{"title":"Marker Assisted Selection (MAS) in Animal Breeding: A Review","authors":"R. Wakchaure, S. Ganguly, P. Praveen, Avinash Kumar, Subhash Sharma, T. Mahajan","doi":"10.4172/2157-7609.1000E127","DOIUrl":"https://doi.org/10.4172/2157-7609.1000E127","url":null,"abstract":"Marker-Assisted Selection (MAS) is a used for indirect selection of superior breeding animals. MAS depend on identifying association between genetic marker and linked Quantitative traits loci (QTL).The association between marker and QTL depend on distance between marker and target traits. As soon as markers linked to QTL have been identified, they can be used in selection programme. This use of marker in selection is called Marker-Assisted Selection. MAS is beneficial when the traits are difficult and expensive to measure and low heritability and recessive traits. MAS facilitate the exploitation of existing genetic diversity in breeding populations and can be used to improve desirable traits in livestock. Marker-Assisted Selection (MAS) is the most widely used application of marker systems in breeding.","PeriodicalId":15537,"journal":{"name":"Journal of Drug Metabolism and Toxicology","volume":"1 1","pages":"1-4"},"PeriodicalIF":0.0,"publicationDate":"2015-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89832781","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abdel-Maksoud A. Hussien, Prof. Mohammed Abdalla Hussein, A. Mageed, A. Abdel-Baky
{"title":"Cranberry Extract as a Functional Food in Treatment of Oxidative Stress in Iron-Induced Hepatic Toxicity in Rats","authors":"Abdel-Maksoud A. Hussien, Prof. Mohammed Abdalla Hussein, A. Mageed, A. Abdel-Baky","doi":"10.4172/2157-7609.1000191","DOIUrl":"https://doi.org/10.4172/2157-7609.1000191","url":null,"abstract":"The present study was to evaluate the protective role of cranberry extract against iron-induced hepatic toxicity in rats. Administration of iron sulfate (30 mg/kg body weight) orally for 21 days, led to significantly (p<0.01) increased in the levels of blood hemoglobin, glucose, lipid profile, plasma and hepatic lipid peroxidation, iron and transferrin. Also, oral administration of iron sulfate showed a significant decrease (p<0.01) in the levels of plasma and liver enzymatic and non-enzymatic antioxidants. Administration of cranberry extract at different doses (75 mg/kg and 150 mg/kg body weight) significantly (p<0.01) restore the levels of plasma and hepatic markers, lipid profile, lipid peroxidation levels as well as increased the levels of plasma and hepatic enzymatic antioxidants and non-enzymatic antioxidants with normalize plasma iron and transferrin concentration in blood. Cranberry extract at a dose of 150 mg/kg body weight exhibits significant protection on hepatic more pronounced than both cranberry 75 mg/kg b.w. and vitamin C. In conclusion, the results clearly suggest that the cranberry extract may be effective in enhances the protection of liver toxicity by its free radical scavenging effect and antioxidant activity.","PeriodicalId":15537,"journal":{"name":"Journal of Drug Metabolism and Toxicology","volume":"36 1","pages":"1-6"},"PeriodicalIF":0.0,"publicationDate":"2015-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79032064","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Fernández, G. Cadenazzi, Mir, a-Mir, K. Larsen, H. Solana
{"title":"A Multienzyme Response is involved in the Phenomenon of Fasciola hepaticaResistance to Triclabendazole","authors":"Fernández, G. Cadenazzi, Mir, a-Mir, K. Larsen, H. Solana","doi":"10.4172/2157-7609.1000192","DOIUrl":"https://doi.org/10.4172/2157-7609.1000192","url":null,"abstract":"The trematode Fasciola hepatica is the causative agent of a parasitic zoonosis known as fasciolosis, disease that affects humans and most species of domestic animals. Triclabendazole (TCBZ) is the most widely used fasciolicide, however, its indiscriminate use has led to the expression of anthelmintic resistance in the liver fluke. In the present work we evaluated “in vitro” the microsomes activity of different xenobiotic metabolizing enzymes of Phase I Carboxylesterases (CE) and Phase II the cytosolic activity of Glutathione S-Transferase (GST), Glutathione peroxidase (GPx) and Glutathione Reductase (GSR) in adults of F. hepatica susceptible (Cullompton strain) and resistant (Sligo and Oberon strains) to triclabendazole. In this work is detected a multienzyme response involving at all the family of enzymes glutathione dependent. Carboxylesterases activity did not differ between the different strains tested not being involved in the resistance phenomenon. These results contribute to the understanding of the mechanisms referred to the phenomenon of resistance to TCBZ.","PeriodicalId":15537,"journal":{"name":"Journal of Drug Metabolism and Toxicology","volume":"6 1","pages":"1-4"},"PeriodicalIF":0.0,"publicationDate":"2015-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81076479","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}