<?xml version="1.0" encoding="utf-8"?>
<Journal>
<Journal-Info>
<name>International Journal of Pharma and Bio Sciences</name>
<website>ijpbs.net</website>
<email>editorijpbs@rediffmail.com (or) editorofijpbs@yahoo.com (or) prasmol@rediffmail.com</email>
</Journal-Info>
<article>
<article-id pub-id-type='other'>10.22376/ijpbs.2019.10.1.p1-12</article-id>
<issue_number>Volume 4 Issue 1</issue_number>
<issue_period>2013 (January - March)</issue_period>
<title>EFFECT OF PROBIOTIC STRAIN LACTOBACILLUS CASEISTRAIN 17 AGAINST TOXICITYINDUCED BY CHROMIUM IN FEMALE REPRODUCTIVE SYSTEM OF RATS. </title>
<abstract>The present study was aimed to investigate whether  lessThan i greaterThan Lactobacillus casei lessThan /i greaterThan  strain17 could protect the chromium (Cr) VI-induced oxidative stress in female reproductive system of rats and to explore the underlying mechanism of the same. A total of 24  lessThan i greaterThan Wistar lessThan /i greaterThan  adult female rats were equally divided into four groups. Group 1 served as control, while groups 2 and 3 were administered K lessThan sub greaterThan 2 lessThan /sub greaterThan Cr lessThan sub greaterThan 2 lessThan /sub greaterThan O lessThan sub greaterThan 7 lessThan /sub greaterThan  (10 mg/kg b.wt. s.c. single dose). In addition to Cr, group 3 also received  lessThan i greaterThan Lactobacillus casei lessThan /i greaterThan (Lc) strain 17 at the rate of 1 x 10 lessThan sup greaterThan 9 lessThan /sup greaterThan  CFU/rat/day for 14 days. Group 4 was maintained as probiotic control (dose as above). Body weights were recorded at the beginning and at the end of experiment. Further the rats were observed for occurrence of estrus cycle. At the end of 14 days, blood samples were drawn for sero-biochemical analysis. Subsequently, all the rats were sacrificed to collect uterus along with ovaries for assay of tissue peroxidation, antioxidant, functional markers and histopathology. Administration of chromium (Cr) VI to rats revealed a significant (p lessThan  0.05) accumulation of cholesterol and a prolonged diestrus phase leading to fertility impairment in rats.Administration of chromium (Cr) VI significantly (p lessThan  0.05) reduced the antioxidant markers such as superoxide dismutase (SOD) and reduced glutathione (GSH), along with significant (p lessThan  0.05) increase in peroxidation markers such as malondialdehyde and protein carbonyls in ovaries. The functional markers in serum such as total protein were decreased whereas other functional markers  lessThan i greaterThan viz lessThan /i greaterThan alanine transaminase (ALT), blood urea nitrogen (BUN) and creatinine were increased. Prominent pathological changes were observed in the uterus and ovaries of Cr-treated group. Co-treatment with  lessThan i greaterThan Lactobacillus casei lessThan /i greaterThan (Lc) strain 17 significantly (p lessThan  0.05) reversed the (Cr) VI induced changes.</abstract>
<authors>C S V SATISH KUMAR, M USHA RANI, K KONDAL REDDY, AND A GOPALA REDDY</authors>
<keywords>Chromium, oxidative stress, Î±-tocopherol, female reproductive system.</keywords>
<pages>1119-1130</pages>
</article>
</Journal>
