Protective Effect of Phycocyanin on Cyclophosphamide-induced Immunocompromised Mice

Objective: To investigate the protective effect of phycocyanin on hepatorenal co-damage in mice caused by cyclophosphamide, and to provide new research ideas for evaluating liver and kidney therapy drugs. Methods: Female BALB/c mice were randomly divided into blank group, model group, positive contr...

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Main Authors: Xinyue LI, Meng ZHAO, Zikang DING, Xiaomei WANG, Ruijun WANG, Zhongshan ZHANG
Format: Article
Language:zho
Published: The editorial department of Science and Technology of Food Industry 2023-05-01
Series:Shipin gongye ke-ji
Subjects:
Online Access:http://www.spgykj.com/cn/article/doi/10.13386/j.issn1002-0306.2022080069
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author Xinyue LI
Meng ZHAO
Zikang DING
Xiaomei WANG
Ruijun WANG
Zhongshan ZHANG
author_facet Xinyue LI
Meng ZHAO
Zikang DING
Xiaomei WANG
Ruijun WANG
Zhongshan ZHANG
author_sort Xinyue LI
collection DOAJ
description Objective: To investigate the protective effect of phycocyanin on hepatorenal co-damage in mice caused by cyclophosphamide, and to provide new research ideas for evaluating liver and kidney therapy drugs. Methods: Female BALB/c mice were randomly divided into blank group, model group, positive control group, high dose group, middle dose group and low dose group. The hepatic and kindy injury model of mice were established by intraperitoneal injection of cyclophosphamide (50, 100, 200 mg/kg), then the mice of blank group and model group were fed with normal saline, mice of positive control group were fed levimidazole hydrochloride (40 mg/kg) and the mice of dosage groups were fed different dosage of instant power of phycocyanin. Interleukin-2 (IL-2), tumournecrosis factor-α (TNF-α), immunoglobulin (IgG), superoxide dismutase (SOD), malondialdehyde (MDA) of serum in mice, superoxide dismutase (SOD), malondialdehyde (MDA), glutathione peroxidase (GSH-Px), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) level of liver tissue and superoxide dismutase (SOD), malondialdehyde (MDA), glutathione peroxidase (GSH-Px), uric acid (UA), urea nitrogenin (BUN) level of kindey tissue in each group mice were determined by reagent kit method. Experimental results showed that compared with the model group, the serum levels of IL-2, TNF-α and MDA in mice in the phycocyanin dose group decreased significantly (P<0.01). The high-dose group of phycocyanin significantly reduced serum IgG levels (P<0.05) and increased serum SOD levels (P<0.05). At the same time, it could reduce the elevated content of MDA in mice caused by cyclophosphamide (P<0.01) and increase SOD activity (P<0.05). In addition, the GSH-Px levels of liver tissue in mice in the phycocyanin dose group were significantly higher than those in the model group (P<0.01), while the levels of MDA, ALT, and AST were significantly lower than those in the model group (P<0.01). Compared with liver tissue, the MDA level of mouse kidney tissue in the phycocyanin dose group was significantly lower than that in the model group (P<0.01), the BUN level of mouse kidney tissue in the low-dose phycocyanin group alone was significantly lower than that in the model group (P<0.01), and the UA level of mouse kidney tissue in the high-dose phycocyanin group was significantly lower than that in the model group (P<0.01). So the powder of phycocyanin had protective effect on cyclophosphamide-induced hepatic and kindy injury in mice.
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spelling doaj.art-58c9589b46d9495ea384c0525d3602ff2023-08-24T06:01:38ZzhoThe editorial department of Science and Technology of Food IndustryShipin gongye ke-ji1002-03062023-05-01441037938610.13386/j.issn1002-0306.20220800692022080069-10Protective Effect of Phycocyanin on Cyclophosphamide-induced Immunocompromised MiceXinyue LI0Meng ZHAO1Zikang DING2Xiaomei WANG3Ruijun WANG4Zhongshan ZHANG5Zhejiang Provincial Key Laboratory of Aquatic Resources Conservation and Development, College of Life Sciences, Huzhou University, Huzhou 313000, ChinaZhejiang Provincial Key Laboratory of Aquatic Resources Conservation and Development, College of Life Sciences, Huzhou University, Huzhou 313000, ChinaZhejiang Provincial Key Laboratory of Aquatic Resources Conservation and Development, College of Life Sciences, Huzhou University, Huzhou 313000, ChinaZhejiang Provincial Key Laboratory of Aquatic Resources Conservation and Development, College of Life Sciences, Huzhou University, Huzhou 313000, ChinaZhejiang Provincial Key Laboratory of Aquatic Resources Conservation and Development, College of Life Sciences, Huzhou University, Huzhou 313000, ChinaZhejiang Provincial Key Laboratory of Aquatic Resources Conservation and Development, College of Life Sciences, Huzhou University, Huzhou 313000, ChinaObjective: To investigate the protective effect of phycocyanin on hepatorenal co-damage in mice caused by cyclophosphamide, and to provide new research ideas for evaluating liver and kidney therapy drugs. Methods: Female BALB/c mice were randomly divided into blank group, model group, positive control group, high dose group, middle dose group and low dose group. The hepatic and kindy injury model of mice were established by intraperitoneal injection of cyclophosphamide (50, 100, 200 mg/kg), then the mice of blank group and model group were fed with normal saline, mice of positive control group were fed levimidazole hydrochloride (40 mg/kg) and the mice of dosage groups were fed different dosage of instant power of phycocyanin. Interleukin-2 (IL-2), tumournecrosis factor-α (TNF-α), immunoglobulin (IgG), superoxide dismutase (SOD), malondialdehyde (MDA) of serum in mice, superoxide dismutase (SOD), malondialdehyde (MDA), glutathione peroxidase (GSH-Px), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) level of liver tissue and superoxide dismutase (SOD), malondialdehyde (MDA), glutathione peroxidase (GSH-Px), uric acid (UA), urea nitrogenin (BUN) level of kindey tissue in each group mice were determined by reagent kit method. Experimental results showed that compared with the model group, the serum levels of IL-2, TNF-α and MDA in mice in the phycocyanin dose group decreased significantly (P<0.01). The high-dose group of phycocyanin significantly reduced serum IgG levels (P<0.05) and increased serum SOD levels (P<0.05). At the same time, it could reduce the elevated content of MDA in mice caused by cyclophosphamide (P<0.01) and increase SOD activity (P<0.05). In addition, the GSH-Px levels of liver tissue in mice in the phycocyanin dose group were significantly higher than those in the model group (P<0.01), while the levels of MDA, ALT, and AST were significantly lower than those in the model group (P<0.01). Compared with liver tissue, the MDA level of mouse kidney tissue in the phycocyanin dose group was significantly lower than that in the model group (P<0.01), the BUN level of mouse kidney tissue in the low-dose phycocyanin group alone was significantly lower than that in the model group (P<0.01), and the UA level of mouse kidney tissue in the high-dose phycocyanin group was significantly lower than that in the model group (P<0.01). So the powder of phycocyanin had protective effect on cyclophosphamide-induced hepatic and kindy injury in mice.http://www.spgykj.com/cn/article/doi/10.13386/j.issn1002-0306.2022080069phycocyanincyclophosphamideliver and kidney injuryprotection
spellingShingle Xinyue LI
Meng ZHAO
Zikang DING
Xiaomei WANG
Ruijun WANG
Zhongshan ZHANG
Protective Effect of Phycocyanin on Cyclophosphamide-induced Immunocompromised Mice
Shipin gongye ke-ji
phycocyanin
cyclophosphamide
liver and kidney injury
protection
title Protective Effect of Phycocyanin on Cyclophosphamide-induced Immunocompromised Mice
title_full Protective Effect of Phycocyanin on Cyclophosphamide-induced Immunocompromised Mice
title_fullStr Protective Effect of Phycocyanin on Cyclophosphamide-induced Immunocompromised Mice
title_full_unstemmed Protective Effect of Phycocyanin on Cyclophosphamide-induced Immunocompromised Mice
title_short Protective Effect of Phycocyanin on Cyclophosphamide-induced Immunocompromised Mice
title_sort protective effect of phycocyanin on cyclophosphamide induced immunocompromised mice
topic phycocyanin
cyclophosphamide
liver and kidney injury
protection
url http://www.spgykj.com/cn/article/doi/10.13386/j.issn1002-0306.2022080069
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AT zikangding protectiveeffectofphycocyaninoncyclophosphamideinducedimmunocompromisedmice
AT xiaomeiwang protectiveeffectofphycocyaninoncyclophosphamideinducedimmunocompromisedmice
AT ruijunwang protectiveeffectofphycocyaninoncyclophosphamideinducedimmunocompromisedmice
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