Lee Young-Hyeon, Kim Hye-Ran, Yeo Min-Ho, Kim Sung-Chun, Hyun Ho-Bong, Ham Young-Min, Jung Yong-Hwan, Kim Hye-Sook, Chang Kyung-Soo
Department of Clinical Laboratory Science, Catholic University of Pusan, Busan 46252, Republic of Korea.
Department of Biomedical Laboratory Science, Dong-Eui Institute of Technology, Busan 47230, Republic of Korea.
Curr Issues Mol Biol. 2023 Sep 13;45(9):7492-7512. doi: 10.3390/cimb45090473.
(SH) and (UA) are marine waste resources that cause environmental and economic problems when entering or multiplying the coastal waters of Jeju Island. We analyzed their anti-diabetic efficacy to assess their reusability as functional additives. The alpha-glucosidase inhibitory activity of SH and UA extracts was confirmed, and the effect of UA extract was higher than that of SH. After the induction of insulin-resistant HepG2 cells, the effects of the two marine extracts on oxidative stress, intracellular glucose uptake, and glycogen content were compared to the positive control, metformin. Treatment of insulin-resistant HepG2 cells with SH and UA resulted in a concentration-dependent decrease in oxidative stress and increased intracellular glucose uptake and glycogen content. Moreover, SH and UA treatment upregulated the expression of , , and , which are suppressed in insulin resistance, to a similar degree to metformin, and suppressed the expression of , involved in gluconeogenesis, and involved in glycogen metabolism. The oral administration of these extracts to rats with streptozotocin-induced diabetes led to a higher weight gain than that in the diabetic group. Insulin resistance and oral glucose tolerance are alleviated by the regulation of blood glucose. Thus, the SH and UA extracts may be used in the development of therapeutic agents or supplements to improve insulin resistance.
(SH)和(UA)是海洋废弃物资源,当它们进入济州岛沿海水域或在其中繁殖时会引发环境和经济问题。我们分析了它们的抗糖尿病功效,以评估其作为功能性添加剂的可再利用性。证实了SH和UA提取物的α-葡萄糖苷酶抑制活性,且UA提取物的效果高于SH。在诱导胰岛素抵抗的HepG2细胞后,将这两种海洋提取物对氧化应激、细胞内葡萄糖摄取和糖原含量的影响与阳性对照二甲双胍进行了比较。用SH和UA处理胰岛素抵抗的HepG2细胞导致氧化应激呈浓度依赖性降低,细胞内葡萄糖摄取和糖原含量增加。此外,SH和UA处理使在胰岛素抵抗中被抑制的、和的表达上调至与二甲双胍相似的程度,并抑制了参与糖异生的和参与糖原代谢的的表达。给链脲佐菌素诱导的糖尿病大鼠口服这些提取物导致体重增加高于糖尿病组。通过调节血糖可缓解胰岛素抵抗和口服葡萄糖耐量。因此,SH和UA提取物可用于开发治疗剂或补充剂以改善胰岛素抵抗。