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Plantago major protects against cisplatin-induced renal dysfunction and tissue damage in rats
by
Hadjzadeh, Musa al-Rida
, Heravi, Nazanin Entezari
, Shahraki, Samirah
, Bideskan, Alirida Ibrahimzadah
, Rad, Abu al-Fadl Khajavi
, Soukhtanloo, Muhammad
, Noshahr, Zahra Samadi
, Parhizgar, Soghra
, Haghshenas, Milad
, Husaynian, Sarah
in
Animals
/ Antioxidants
/ Apoptosis
/ Chemotherapy
/ Drinking water
/ Experiments
/ Gangrene
/ Kidneys
/ Medical research
/ Oxidative stress
/ Potassium
/ Rodents
/ Studies
/ Urine
2018
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Plantago major protects against cisplatin-induced renal dysfunction and tissue damage in rats
by
Hadjzadeh, Musa al-Rida
, Heravi, Nazanin Entezari
, Shahraki, Samirah
, Bideskan, Alirida Ibrahimzadah
, Rad, Abu al-Fadl Khajavi
, Soukhtanloo, Muhammad
, Noshahr, Zahra Samadi
, Parhizgar, Soghra
, Haghshenas, Milad
, Husaynian, Sarah
in
Animals
/ Antioxidants
/ Apoptosis
/ Chemotherapy
/ Drinking water
/ Experiments
/ Gangrene
/ Kidneys
/ Medical research
/ Oxidative stress
/ Potassium
/ Rodents
/ Studies
/ Urine
2018
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Plantago major protects against cisplatin-induced renal dysfunction and tissue damage in rats
by
Hadjzadeh, Musa al-Rida
, Heravi, Nazanin Entezari
, Shahraki, Samirah
, Bideskan, Alirida Ibrahimzadah
, Rad, Abu al-Fadl Khajavi
, Soukhtanloo, Muhammad
, Noshahr, Zahra Samadi
, Parhizgar, Soghra
, Haghshenas, Milad
, Husaynian, Sarah
in
Animals
/ Antioxidants
/ Apoptosis
/ Chemotherapy
/ Drinking water
/ Experiments
/ Gangrene
/ Kidneys
/ Medical research
/ Oxidative stress
/ Potassium
/ Rodents
/ Studies
/ Urine
2018
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Plantago major protects against cisplatin-induced renal dysfunction and tissue damage in rats
Journal Article
Plantago major protects against cisplatin-induced renal dysfunction and tissue damage in rats
2018
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Overview
The aim of the present study was to determine the effect of Plantago major (P.
major) on cisplatin-induced kidney injury in the rat. Cisplatin was injected on the 6th day of the
experiment. Animals were treated with P. major extract (300, 600, and 1200 mg/kg) and Vitamin
E for five days before and two weeks after cisplatin administration. Cisplatin caused a significant
decrease in glomerular filtration rate (GFR), urine osmolarity, and urinary excretion rate of
potassium, but significant increase in the kidney index and histological damage compared with
the control group. Administration of Vitamin E and P. major (300 and 600 mg/kg) significantly
increased GFR compared to cisplatin group. Furthermore, urine osmolarity in Vitamin E and P. major (600 mg/kg) groups were significantly elevated compared to the cisplatin group. P. major
(600 mg/kg) significantly increased the urinary excretion rate of potassium compared with
cisplatin group. Furthermore, all doses of P. major and Vitamin E significantly attenuated the
percentage of kidney tissue damage compared to the cisplatin group. However, only P. major
(600 mg/kg) and Vitamin E treated rats showed a significant reduction in the kidney index. This
study revealed that P. major extract in a dose-dependent manner provides protection against renal
damage induced by cisplatin.
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