Salvador Ângelo C, Król Ewelina, Lemos Virgínia C, Santos Sónia A O, Bento Fernanda P M S, Costa Carina P, Almeida Adelaide, Szczepankiewicz Dawid, Kulczyński Bartosz, Krejpcio Zbigniew, Silvestre Armando J D, Rocha Sílvia M
Organic Chemistry, Natural Products and Food Stuffs Research Unit, QOPNA, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal.
Aveiro Institute of Materials, CICECO, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal.
Int J Mol Sci. 2016 Dec 22;18(1):13. doi: 10.3390/ijms18010013.
Elderberry ( L.) lipophilic and polar extract dietary supplementation effects were evaluated according to diabetes management indices, using an in vivo model. A research pipeline was constructed, that ranged from extract preparation, partial chemical characterization and toxicity evaluation, to examining the elderberry extract dietary supplementation effects on biofluid and tissues. Extracts toxicity was screened using an bioluminescence model. A concentration of up to 60 mg/L was selected, and rat doses for oral supplementation were computed applying the interspecies correlation between and rats. Wistar type 2 diabetic rats, induced by streptozotocin (STZ), were fed a high-fat diet and supplemented for 4 weeks at doses of 190 and 350 mg/kg body weight/day of lipophilic and polar extract, respectively. As far as we know, lipophilic elderberry extract supplementation was assessed for the first time, while polar extract was administrated at higher doses and for a shorter period compared to previous studies, aiming to evaluate subacute supplementation effects. The polar extract modulated glucose metabolism by correcting hyperglycemia, while the lipophilic extract lowered insulin secretion. Both extracts lowered insulin resistance, without remarkable alterations to hematological indices, sera lipids and sera and tissular trace element homeostasis. In conclusion, elderberries are a potential source of bioactive compounds for formulations to be used as co-adjuvants in diabetes management.
采用体内模型,根据糖尿病管理指标评估接骨木(L.)亲脂性和极性提取物膳食补充剂的效果。构建了一个研究流程,涵盖提取物制备、部分化学表征和毒性评估,直至研究接骨木提取物膳食补充剂对生物流体和组织的影响。使用生物发光模型筛选提取物的毒性。选择高达60 mg/L的浓度,并根据与大鼠之间的种间相关性计算大鼠口服补充剂的剂量。用链脲佐菌素(STZ)诱导的Wistar 2型糖尿病大鼠,喂食高脂饮食,并分别以190和350 mg/kg体重/天的剂量补充亲脂性和极性提取物4周。据我们所知,首次评估了亲脂性接骨木提取物的补充情况,而与先前的研究相比,极性提取物以更高的剂量和更短的时间给药,旨在评估亚急性补充效果。极性提取物通过纠正高血糖来调节葡萄糖代谢,而亲脂性提取物降低胰岛素分泌。两种提取物均降低胰岛素抵抗,对血液学指标、血清脂质以及血清和组织微量元素稳态无明显改变。总之,接骨木是一种潜在的生物活性化合物来源,可用于制备在糖尿病管理中用作辅助剂的制剂。