The protective effect of betulinic acid on microvascular responsivity and protein expression in alzheimer disease induced by cerebral micro‐injection of beta‐amyloid and streptozotocin. (8th October 2018)

• Record Type: Journal Article
• Authors: Sarkaki, Alireza; Farbood, Yaghoob; Badavi, Mohammad; Ghadiri, Ata; Ghasemi dehcheshmeh, Mohammad; Mansouri, Esrafil; Navabi, Seyedeh Parisa
• Is Part Of: Microcirculation. Volume 25:Number 8(2018)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2018-10-08
• Subjects: alzheimer's disease -- betulinic acid -- blood‐brain barrier -- brain‐derived neurotrophic factor -- microcirculation -- tumor necrosis factor alpha; Biological transport -- Periodicals; Microcirculation -- Physiology -- Periodicals; 612.135
• DOI: 10.1111/micc.12503
• Languages: English
• ISSNs: 1073-9688

Abstract

Abstract: Objective: Alzheimer's disease (AD) is mainly caused by accumulation of β‐amyloid (Aβ) in vessels or parenchyma of the brain. Accordingly, natural compounds such as betulinic acid (BA) might improve the AD signs by increase in blood flow and through reduction in amyloid plaques. Methods: Intra‐hippocampal injection of BA (0.2 and 0.4 μmol/L /10 μL DMSO /rat) was done at intervals of 180 and 10 min before co‐microinjection of 0.1 μmol/L Aβ dissolved in PBS (5 μL/rat, hippocampi) and 1.5 mg/kg Streptozotocin dissolved in aCSF (10 μL/rat, lateral ventricles). Cerebro‐vascular responsivity tested by Laser Doppler, BBB leakage, Elisa assays of cytokines (TNF‐α and IL‐10), and Western blot analysis of proteins (BDNF and AchE) in the hippocampus were assessed 1 month after the injections. Results: Microvascular reaction and BBB function were significantly impaired in AD rats, which were improved via BA pretreatment. BA could increase BDNF expression and decrease cytokine levels in the hippocampus of AD rats (especially 0.1 μmol/L Aβ: 0.4 μmol/L BA); however, no significant changes were detected in the blotting of AchE among the groups. Conclusions: Betulinic acid could have a role in AD through protecting microcirculation, alleviating inflammation, and up‐regulating BDNF expression which is clearer toward 1:4 molar ratios of Aβ to BA.