Indirect Chronic Effects of an Oleuropein-Rich Olive Leaf Extract on Sucrase-Isomaltase In Vitro and In Vivo.
Alison PynerShuk Yan ChanSarka TumovaAsimina KerimiGary WilliamsonPublished in: Nutrients (2019)
Consumption of dietary bioactives is an avenue to enhancing the effective healthiness of diets by attenuating the glycaemic response. The intestinal brush border enzyme sucrase-isomaltase (SI) is the sole enzyme hydrolysing consumed sucrose, and we previously showed the acute effects of olive leaf extract (OLE) on sucrase activity when given together with sugars both in vitro and in vivo. Here we tested whether OLE could affect sucrase expression when pre-incubated chronically, a "priming" effect not dependent on competitive interaction with SI, in both a cell model and a human intervention. Using differentiated Caco-2/TC7 cells, long-term pre-treatment with oleuropein-rich olive leaf extract (OLE) lowered SI mRNA, surface protein and activity, and attenuated subsequent sucrose hydrolysis. Based on these results, a randomised, double-blinded, placebo-controlled, crossover pilot study was conducted. OLE (50 mg oleuropein) was consumed in capsule form 3 times a day for 1 week by 11 healthy young women followed by an oral sucrose tolerance test in the absence of OLE. However this treatment, compared to placebo, did not induce a change in post-prandial blood glucose maximum concentration (Glcmax), time to reach Glcmax and incremental area under the curve. These results indicate that changes in SI mRNA, protein and activity in an intestinal cell model by OLE are not sufficient under these conditions to induce a functional effect in vivo in healthy volunteers.
Keyphrases
- placebo controlled
- blood glucose
- double blind
- binding protein
- room temperature
- randomized controlled trial
- clinical trial
- open label
- single cell
- cell therapy
- type diabetes
- study protocol
- induced apoptosis
- poor prognosis
- adipose tissue
- phase iii
- cell cycle arrest
- weight loss
- drug induced
- amino acid
- cell death
- skeletal muscle
- radiation therapy
- ionic liquid
- mesenchymal stem cells
- signaling pathway
- small molecule
- extracorporeal membrane oxygenation
- respiratory failure