The potent therapeutic effect of novel cyanobacterial isolates against oxidative stress damage in redox rats
Journal of applied microbiology • 2019
معلومات البحث
المؤلفون
Omnia AM Badr, Ibrahim IS EL‐Shawaf, Hoda AS El‐Garhy, Mahmoud MA Moustafa, Omar A Ahmed‐Farid
الكلمات المفتاحية
Cyanobacteria, Antioxidant activity, liver functions, Oxidative stress, Redox rats, Caspase
-
3 qRT-PCR
.
المجلة العلمية
Journal of applied microbiology
الناشر
Wiley
المجلد
126,
العدد
(2019)
الصفحات
1278--1289
publication.type
International
رابط البحث
Open Link
المواد المرفقة
Not Available
الملخص
Aims
Cyanobacteria are immense sources of several pharmacological active compounds such as flavonoids and carotenoids with anti‐inflammatory and antioxidant activity. The potential therapeutic effect of two novel cyanobacterial isolates, Cronbergia siamensis (KY296358.1) and Sphaerospermopsis aphanizomenoides (KU212886.1), against hydrogen peroxide‐induced oxidative stress damage in the rat model was determined in this study.
Methods and Results
In vitro antioxidant activity of the two studied isolates was evaluated by radical scavenging assay and ferric reducing power. The possible prophylactic activity of S. aphanizomenoides (KU212886.1) against hydrogen peroxide‐induced oxidative stress in the rat model was assessed in vivo. Serum alanine transaminase (ALT) and aspartate transaminase (AST) were measured for the liver functions in redox rats. Liver malondialdehyde (MDA), glutathione (GSH), oxidized glutathione (GSSG), nitric oxide (NO), superoxide dismutase (SOD) and catalase (CAT) were assessed as oxidative stress markers. The effect of S. aphanizomenoides on the transcripts level of superoxide dismutase (Mn‐SOD) and catalase (CAT) genes in the rat's liver tissues was measured using qRT‐PCR. Oral administration of S. aphanizomenoides extract in low and high doses (100, 200 mg kg−1 b.w) resulted in significant improvement in biochemical parameters of liver functions and oxidative stress markers. Also, the endogenous antioxidant defense enzymes and the expression of their related genes (Mn/SOD, CAT) were upregulated. Immunohistochemistry of Caspase‐3, an apoptotic marker, showed potent amelioration in the liver tissues.
Conclusions
The novel isolate S. aphanizomenoides proved in vitro and in vivo antioxidant activity against redox rat model.
Cyanobacteria are immense sources of several pharmacological active compounds such as flavonoids and carotenoids with anti‐inflammatory and antioxidant activity. The potential therapeutic effect of two novel cyanobacterial isolates, Cronbergia siamensis (KY296358.1) and Sphaerospermopsis aphanizomenoides (KU212886.1), against hydrogen peroxide‐induced oxidative stress damage in the rat model was determined in this study.
Methods and Results
In vitro antioxidant activity of the two studied isolates was evaluated by radical scavenging assay and ferric reducing power. The possible prophylactic activity of S. aphanizomenoides (KU212886.1) against hydrogen peroxide‐induced oxidative stress in the rat model was assessed in vivo. Serum alanine transaminase (ALT) and aspartate transaminase (AST) were measured for the liver functions in redox rats. Liver malondialdehyde (MDA), glutathione (GSH), oxidized glutathione (GSSG), nitric oxide (NO), superoxide dismutase (SOD) and catalase (CAT) were assessed as oxidative stress markers. The effect of S. aphanizomenoides on the transcripts level of superoxide dismutase (Mn‐SOD) and catalase (CAT) genes in the rat's liver tissues was measured using qRT‐PCR. Oral administration of S. aphanizomenoides extract in low and high doses (100, 200 mg kg−1 b.w) resulted in significant improvement in biochemical parameters of liver functions and oxidative stress markers. Also, the endogenous antioxidant defense enzymes and the expression of their related genes (Mn/SOD, CAT) were upregulated. Immunohistochemistry of Caspase‐3, an apoptotic marker, showed potent amelioration in the liver tissues.
Conclusions
The novel isolate S. aphanizomenoides proved in vitro and in vivo antioxidant activity against redox rat model.
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