Author/Authors :
Miri, Saide Department of Physiology - Zahedan University of Medical Sciences, Zahedan, Iran , Safari, Tahereh Department of Physiology - Zahedan University of Medical Sciences, Zahedan, Iran , Komeili, Gholam Reza Department of Physiology - Zahedan University of Medical Sciences, Zahedan, Iran , Nematbakhsh, Mehdi Department of Physiology - Water and Electrolytes Research Center - Isfahan University of Medical Sciences, Isfahan, Iran , Niazi, Abbass Ali Department of Pathology - Zahedan University of Medical Sciences, Zahedan, Iran , Jahantigh, Mehdi Department of Pathology - Zahedan University of Medical Sciences, Zahedan, Iran , Bagheri, Hossein Department of Medical English - Zahedan University of Medical Sciences, Zahedan, Iran , Maghool, Fatemeh Department of Physiology - Isfahan University of Medical Sciences, Isfahan, Iran
Abstract :
Background: L‑arginine is an important precursor for the formation of nitric oxide (NO). According
to previous studies, NO function is related to gender. Likewise, chronic renal diseases have lower
prevalence in female. Gentamicin (GM) is an aminoglycoside antibiotic. According to some studies,
males are more sensitive to GM renal nephrotoxicity. This study attempts to find protective effects
of L‑arginine on GM nephrotoxicity in male and female rats. Methods: Male and female rats were
divided into eight groups: Rats were randomly assigned to 8 groups each including both male and
female rats. The first and second groups received vehicle (saline), the third and fourth groups
received gentamicin (80 mg/kg), the fifth and sixth groups received L‑arginine (150 mg/kg), and
finally, seventh and eighth groups received gentamicin+ L- arginine. Next, 9 days after administering
drugs, blood samples were collected from the heart. After making sacrifices, the level of blood urea,
creatinine (Cr), nitrite, and malondialdehyde (MDA) was measured in serums. Likewise, nitrite
and MDA were measured in the homogenized kidney tissue. Results: GM significantly increased
serum level of urea and Cr in male and female rats (P < 0.05). However, co‑administration of
GM + L‑arginine significantly did not decrease urea and Cr level in male rats, whereas, in female
rats, they significantly reduced (P < 0.05). In response to GM, renal MDA level increased in male
and female rats (P < 0.05), and in the presence of GM + L‑arginine, the level of MDA significantly
decreased in both genders (P < 0.05). Conclusions: L‑arginine demonstrated some protective effects
in female rats but did not protect against GM nephrotoxicity in male rats for unknown reasons,
probably related to the effects of sex hormones which needs further studies to be confirmed.
Keywords :
Gentamicin , L‑arginine , Nephrotoxicity , Sex difference