سامانه مدیریت نشریات علمی دانشگاه علوم پزشکی مشهد

Bazmandegan, Gholamreza, Amirteimoury, Morteza, Kaeidi, Ayat, Shamsizadeh, Ali, Khademalhosseini, Morteza, Nematollahi, Mohammad Hadi, hasanipoor, mahsa, Fatemi, Iman. (1398). Sumatriptan ameliorates renal injury induced by cisplatin in mice. , 22(5), 563-567. doi: 10.22038/ijbms.2019.33620.8020
Gholamreza Bazmandegan; Morteza Amirteimoury; Ayat Kaeidi; Ali Shamsizadeh; Morteza Khademalhosseini; Mohammad Hadi Nematollahi; mahsa hasanipoor; Iman Fatemi. "Sumatriptan ameliorates renal injury induced by cisplatin in mice". , 22, 5, 1398, 563-567. doi: 10.22038/ijbms.2019.33620.8020
Bazmandegan, Gholamreza, Amirteimoury, Morteza, Kaeidi, Ayat, Shamsizadeh, Ali, Khademalhosseini, Morteza, Nematollahi, Mohammad Hadi, hasanipoor, mahsa, Fatemi, Iman. (1398). 'Sumatriptan ameliorates renal injury induced by cisplatin in mice', , 22(5), pp. 563-567. doi: 10.22038/ijbms.2019.33620.8020
Bazmandegan, Gholamreza, Amirteimoury, Morteza, Kaeidi, Ayat, Shamsizadeh, Ali, Khademalhosseini, Morteza, Nematollahi, Mohammad Hadi, hasanipoor, mahsa, Fatemi, Iman. Sumatriptan ameliorates renal injury induced by cisplatin in mice. , 1398; 22(5): 563-567. doi: 10.22038/ijbms.2019.33620.8020

Sumatriptan ameliorates renal injury induced by cisplatin in mice

Iranian Journal of Basic Medical Sciences
مقاله 15، دوره 22، شماره 5، مرداد 2019، صفحه 563-567    اصل مقاله (764.5 K)
نوع مقاله: Original Article
شناسه دیجیتال (DOI): 10.22038/ijbms.2019.33620.8020
نویسندگان
Gholamreza Bazmandegan1، 2؛ Morteza Amirteimoury3؛ Ayat Kaeidi1، 4؛ Ali Shamsizadeh1، 4؛ Morteza Khademalhosseini5؛ Mohammad Hadi Nematollahi6؛ mahsa hasanipoor1، 4؛ Iman Fatemi* 1، 4
1Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran
2Non-Communicable Diseases Research Center, Rafsanjan University of Medical Sciences, Rafsanjan, Iran
3Clinical Research Development Center, Ali Ibn Abitaleb Hospital, Rafsanjan University of Medical Sciences, Rafsanjan, Iran
4Department of Physiology and Pharmacology, Rafsanjan University of Medical Sciences, Rafsanjan, Iran
5Department of Pathology, Rafsanjan University of Medical Sciences, Rafsanjan, Iran
6Department of Clinical Biochemistry, Kerman University of Medical Sciences, Kerman, Iran
چکیده
Objective(s): Cisplatin (Cis) is an anticancer compound, which is used for the treatment of various cancers. Sumatriptan (Suma) is a selective agonist of 5-hydroxytryptamine 1B/1D (5HT1B/1D) receptor, which is prescribed for the management of migraine. It is well-established that Suma has anti-inflammatory and antioxidant properties. We have explored the protective effects of Suma in the mitigation of Cis-induced nephrotoxicity.
Materials and Methods: The mice received a single IP injection of Cis (20 mg/kg) on the first day of the experiment. Suma treatment (0.1 and 0.3 mg/kg/day, IP) was started on day 1 and continued for 3 consecutive days.
Results: Creatinine (Cr), blood urea nitrogen (BUN) and malondialdehyde (MDA) levels were elevated and glutathione peroxidase (GPx) as well as superoxide dismutase (SOD) activities were decreased in Cis-treated mice. Suma (more potently 0.3 mg/kg) reduced Cr, BUN and MDA levels and increased SOD and GPx levels. Suma also reduced the acute renal injury (tubular degeneration, tubular cells vacuolation, tubular necrosis and cast), which corresponded to kidney damage in Cis-treated mice.
Conclusion: These findings demonstrate that Suma mitigates Cis-induced renal injury by inhibition of oxidative stress and enhancing the antioxidant enzymes activities.
کلیدواژه‌ها
Cisplatin؛ Mice؛ Nephrotoxicity؛ Oxidative stress؛ Sumatriptan
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