Favourable effect of ß-glucan treatment against cisplatin-induced reproductive system damage in male rats

Autor: Kürşat Kaya, Asli Cetin, Nese Basak, Osman Ciftci, M. Aydin
Jazyk: angličtina
Rok vydání: 2019
Předmět:
reproductive toxicity
Male
antioxidant
Antioxidant
beta-Glucans
medicine.medical_treatment
030232 urology & nephrology
cisplatin
animal cell
reactive oxygen metabolite
Pharmacology
medicine.disease_cause
Antioxidants
Lipid peroxidation
Rats
Sprague-Dawley

chemistry.chemical_compound
0302 clinical medicine
Endocrinology
Testis
oxidative stress
Medicine
rat
animal
glutathione
glutathione peroxidase
antineoplastic agent
Sperm motility
male genital system disease
chemistry.chemical_classification
Epididymis
030219 obstetrics & reproductive medicine
imuneks
Sprague Dawley rat
biology
Sperm Count
beta glucan
adult
Glutathione peroxidase
catalase
drug effect
lipid peroxidation
General Medicine
superoxide dismutase
spermiotoxicity
enzyme activity
spermatozoon count
histopathology
Sperm Motility
medicine.drug
Urology
thiobarbituric acid reactive substance
animal experiment
testis tissue
?-glucan
β-glucan
Antineoplastic Agents
Testicular Diseases
Thiobarbituric Acid Reactive Substances
Article
animal tissue
histology
Superoxide dismutase
03 medical and health sciences
testicular damage
Animals
Humans
controlled study
human
Antineoplastic Agents/*adverse effects
Antioxidants/*administration & dosage
Cisplatin/*adverse effects
Disease Models
Animal

Epididymis/drug effects/pathology
Lipid Peroxidation/drug effects
Oxidative Stress/drug effects
Rats
Sperm Motility/drug effects
Testicular Diseases/chemically induced/pathology/*prevention & control
Testis/drug effects/pathology
Thiobarbituric Acid Reactive Substances/metabolism
beta-Glucans/*administ
Cisplatin
spermatozoon density
nonhuman
treatment duration
business.industry
animal model
spermatozoon motility
disease model
Glutathione
Oxidative Stress
chemistry
organ weight
testis disease
biology.protein
pathology
Lipid Peroxidation
business
metabolism
Oxidative stress
DOI: 10.1111/and.13342.
Popis: The aim of this study was to investigate the potential beneficial effects of β-glucan treatment against oxidative, histological and spermatological damage caused by cisplatin on the male reproductive system. Twenty-eight Sprague Dawley male rats were used in the study. The rats were randomly divided into four equal-sized groups: a control group, cisplatin group (7 mg/kg in a single-dose cisplatin administered intraperitoneally), β-glucan group (β-glucan given at a dose of 50 mg kg−1 d−1 for 14 day) and a cisplatin plus β-glucan group (cisplatin and β-glucan administered together at the same dose). Cisplatin administration induced an increase in the level of thiobarbituric acid-reactive substances, a lipid peroxidation indicator. It induced a decrease in enzymatic (superoxide dismutase, catalase and glutathione peroxidase) activities and nonenzymatic (reduced glutathione) antioxidant levels. In addition, cisplatin caused both histological and spermatological damage, as shown by a decrease in sperm motility and epididymal sperm concentrations and an increase in abnormal sperm rates. The β-glucan treatment improved cisplatin-induced oxidative, histological and spermatological damage. This study revealed that β-glucan treatment provided prevention against male reproductive system damage caused by cisplatin. These preventative effects were likely due to its antioxidant properties. © 2019 Blackwell Verlag GmbH
Databáze: OpenAIRE