Literature DB >> 26452500

Protective effect of rosmarinic acid against oxidative stress biomarkers in liver and kidney of strepotozotocin-induced diabetic rats.

Nadia Mushtaq1, Roberta Schmatz2,3, Mushtaq Ahmed4, Luciane Belmonte Pereira1, Pauline da Costa1, Karine Paula Reichert1, Diéssica Dalenogare1, Luana Paula Pelinson1, Juliano Marchi Vieira1, Naiara Stefanello1, Lizielle Souza de Oliveira1, Nadia Mulinacci5, Maria Bellumori5, Vera Maria Morsch1, Maria Rosa Schetinger6.   

Abstract

In the present study, we investigated the efficiency of rosmarinic acid (RA) in preventing the alteration of oxidative parameters in the liver and kidney of diabetic rats induced by streptozotocin (STZ). The animals were divided into six groups (n = 8): control, ethanol, RA 10 mg/kg, diabetic, diabetic/ethanol, and diabetic/RA 10 mg/kg. After 3 weeks of treatment, we found that TBARS levels in liver and kidney were significantly increased in the diabetic/saline group and the administration of RA prevented this increase in the liver and kidney (P < 0.05). Diabetes caused a significant decrease in the activity of superoxide dismutase (SOD) and catalase (CAT) in the diabetes/saline group (P < 0.05). However, the treatment with 10 mg/kg RA (antioxidant) prevented this alteration in SOD and CAT activity in the diabetic RA group (P < 0.05). In addition, RA reverses the decrease in ascorbic acid and non-protein-thiol (NPSH) levels in diabetic rats. The treatment with RA also prevented the decrease in the Delta-aminolevulinic acid dehydratase (ALA-D) activity in the liver and kidney of diabetic rats. Furthermore, RA did not have any effect on glycemic levels. These results indicate that RA effectively reduced the oxidative stress induced by STZ, suggesting that RA is a potential candidate for the prevention and treatment of pathological conditions in diabetic models.

Entities:  

Keywords:  Oxidative stress; Rosmarinic acid; Strepotozotocin

Mesh:

Substances:

Year:  2015        PMID: 26452500     DOI: 10.1007/s13105-015-0438-4

Source DB:  PubMed          Journal:  J Physiol Biochem        ISSN: 1138-7548            Impact factor:   4.158


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