Wiśniewski Karol, Zglejc-Waszak Kamila, Antonowski Tomasz, Szablinska-Piernik Joanna, Juskiewicz Jerzy, Lahuta Lesław, Jozwik Marcin, Wojtkiewicz Joanna
Students' Scientific Club of Pathophysiologists, Department of Human Physiology and Pathophysiology, School of Medicine, University of Warmia and Mazury in Olsztyn, 10-082 Olsztyn, Poland.
Department of Anatomy and Histology, School of Medicine, Collegium Medicum, University of Warmia and Mazury in Olsztyn, 10-085 Olsztyn, Poland.
Pharmaceuticals (Basel). 2025 Jun 25;18(7):954. doi: 10.3390/ph18070954.
: Scyllo-inositol (SCI) is a naturally occurring carbocyclic sugar implicated in many biological processes. Studies have highlighted the potential of using SCI in Alzheimer's therapy. However, in order to fully use this compound in the treatment of neurovegetative diseases, its pharmacokinetics must be thoroughly understood. : We undertook the task of analyzing SCI in a Wistar rat animal model. The aim of this study was to observe the changes in SCI concentration after oral administration. : All rats received 10 mg/kg of SCI as a solution in distilled water by oral gavage. Estimated parameters were based on the serum concentration of SCI observed in six individual rats with regard to time. : The first peak concentration appeared at 30 min for SCI. Thereafter, the serum SCI concentration increased rapidly and reached its highest level after approximately 1.5 h. There was no second peak in SCI concentration. The elimination half-life was determined to be 10.07 h and the mean residence time was 14.52 h. There were no side effects of SCI supplementation noticed during the study. : Although our results present an analysis of SCI immediately after oral administration up to 48 h, further studies are necessary.
scyllo-肌醇(SCI)是一种天然存在的碳环糖,参与许多生物过程。研究突出了将SCI用于阿尔茨海默病治疗的潜力。然而,为了在治疗神经植物性疾病中充分利用这种化合物,必须彻底了解其药代动力学。
我们承担了在Wistar大鼠动物模型中分析SCI的任务。本研究的目的是观察口服给药后SCI浓度的变化。
所有大鼠通过口服灌胃接受10mg/kg SCI的蒸馏水溶解液。估计参数基于六只个体大鼠中观察到的SCI血清浓度随时间的变化。
SCI的第一个峰值浓度出现在30分钟。此后,血清SCI浓度迅速上升,约1.5小时后达到最高水平。SCI浓度没有第二个峰值。消除半衰期确定为10.07小时,平均驻留时间为14.52小时。研究期间未发现补充SCI有副作用。
虽然我们的结果呈现了口服给药后直至48小时的SCI分析,但仍需要进一步研究。