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Original Article:
Effects of probiotic supplementation on pancreatic β-cell function and c-reactive protein in women with polycystic ovary syndrome: A randomized double-blind placebo-controlled clinical trial
Tanaz Shoaei, Motahar Heidari-Beni, Hatav Ghasemi Tehrani, Awat feizi, Ahmad Esmaillzadeh, Gholamreza Askari
Int J Prev Med
2015, 6:27 (24 March 2015)
DOI
:10.4103/2008-7802.153866
PMID
:25949777
Background:
Polycystic ovary syndrome (PCOS) is a polygenic endocrine disorder in women of reproductive age that lead to infertility. The aim of this study was to investigate the effects of probiotic on pancreatic b-cell function and C-reactive protein (CRP) in PCOS patients.
Methods:
This randomized double-blind placebo-controlled clinical trial was conducted among 72 women aged 15-40 years old diagnosed with PCOS. Participants were randomly assigned to two groups receiving: (1) Probiotic supplements (
n
= 36), (2) placebo (
n
= 36) for 8-week. Fasting blood samples were taken at baseline and after 8-week of intervention.
Results:
Probiotic supplementation, compare with placebo, reduced fasting blood sugar (−4.15 ± 2.87 vs. 2.57 ± 5.66 mg/dL, respectively
P
= 0.7), serum insulin levels in crude model (−0.49 ± 0.67 vs. 0.34 ± 0.82 mIU/mL, respectively,
P
= 0.09), homeostasis model of assessment-insulin resistance score (−0.25 ± 0.18 vs. −0.05 ± 0.18, respectively,
P
= 0.14) nonsignificantly. Serum insulin levels after adjustment with covariates reduced significantly in probiotic group (
P
= 0.02). We did not found any significant differences in mean changes of CRP between groups (−0.25 ± 0.18 vs. −0.05 ± 0.18, respectively,
P
= 0.14).
Conclusions:
A 8-week multispecies probiotics supplementation had nonsignificantly beneficial effect on pancreatic b-cell function and CRP in PCOS patients. After adjustment for some covariates, serum insulin changes were significantly different between groups.
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Original Article:
Preventive role of estradiol on kidney injury induced by renal Ischemia-Reperfusion in male and female rats
Akram Iran-Nejad, Mehdi Nematbakhsh, Fatemeh Eshraghi-Jazi, Ardeshir Talebi
Int J Prev Med
2015, 6:22 (20 March 2015)
DOI
:10.4103/2008-7802.153537
PMID
:25830011
Background:
Renal ischemia-reperfusion (RIR) is the main cause of renal failure. The incidence of RIR injury seems to be gender-related due to female sex hormone; estrogen. This study was designed to investigate the protective role of estrogen against RIR injury in male and ovariectomized female rats.
Methods:
Thirty-nine Wistar rats were used in this study as male and ovariectomized female rats in the sham-operated, RIR, and estradiol-treated plus RIR groups. The RIR was induced by clamping the renal vessels for 45 min and then 24 h of reperfusion. All animals finally were sacrificed for the measurements.
Results:
The serum levels of creatinine and blood urea nitrogen and kidney tissue damage score significantly increased in both male and female RIR rats (
P
< 0.05). Estradiol however significantly attenuated theses parameters (
P
< 0.05) toward normal levels in female (
P
< 0.05), but not in male rats. Kidney weight increased in both genders and estradiol intensified it in the male rats (
P
< 0.05). Uterus weight was increased by estradiol in female rats (
P
< 0.05) and testis weight did not alter in male rats.
Conclusions:
Estradiol demonstrated a protective role against RIR injury in female rats; however, estradiol as an antioxidant could not protect the male kidney from RIR injury.
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© International Journal of Preventive Medicine | Published by Wolters Kluwer -
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Online since 2
nd
January, 2015