Aqueous chicory seed extract ameliorates diabetic kidney damage via alteration of renal renin-angiotensin system (RAS) balance
Abstract
Objectives: This study investigated the effects of aqueous chicory seed extract (CSE),metformin (Met), and aspirin (Asp) on the Renin-Angiotensin System (RAS) in healthyWistar rats, as well as in early (NIA/STZ) and late-stage diabetes (STZ).
Methods: Rats were divided into Control, NIA/STZ, and STZ groups. NIA/STZ ratsreceived niacinamide/streptozotocin, while STZ rats received STZ to induce early andlate stages of diabetes. Subgroups received CSE (125 mg/kg), metformin (100 mg/kg),or aspirin (120 mg/kg). Measurements included mRNA levels of AGT, ACE, and ACE2;activities of ACE and ACE2; levels of Ang II and Ang-(1-7); protein carbonyl content(PCC); nitric oxide (NO); and kidney collagen.
Results: Late-stage diabetes (STZ) decreased AGT, ACE, and ACE2 mRNA, butincreased ACE activity, Ang II, Ang-(1-7), the ACE/ACE2 ratio, PCC, and collagen.CSE increased AGT and ACE2 mRNA, and decreased ACE activity, Ang II, the ACE/ACE2 ratio, and PCC. Metformin boosted AGT mRNA and reduced PCC and collagen.Aspirin lowered collagen. Early diabetes (NIA/STZ) decreased AGT, ACE2, and Ang-(1-7), while increasing ACE activity and Ang II levels. CSE increased AGT and Ang-(1-7), and reduced Ang II and the Ang II/Ang-(1-7) ratio. Metformin reduced ACE mRNAand increased Ang-(1-7). CSE decreased reactive oxygen species (ROS) and improvedAng-(1-7) levels, especially in early stages. Both CSE and metformin helped reducefibrosis.
Conclusion: Our findings suggest that CSE supports renal tissue repair in both early andlate stages of T2D by increasing levels of the protective peptide Ang-(1-7).