Kaempferol treatment ameliorates memory impairments in STZ‑induced neurodegeneration by acting on reelin signaling.

IF 1.4 4区 医学 Q4 NEUROSCIENCES Acta neurobiologiae experimentalis Pub Date : 2023-09-29 DOI:10.55782/ane-2023-2427
Melike Uysal, Mert Celikten, Merve Beker, Nurhayat Polat, Onder Huseyinbas, Sule Terzioglu-Usak, Birsen Elibol
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引用次数: 1

Abstract

Many treatment initiatives, like herbal products and their active ingredients, aim to alleviate neurodegeneration to increase cognitive functions. Kaempferol may be a candidate molecule for treating neurodegeneration because of its antioxidant effects. In the present study, we examined the molecular changes associated with kaempferol's memory‑enhancing effects on streptozotocin (STZ)‑induced neurodegeneration. After intracerebroventricular STZ injection in Long‑Evans male rats, intraperitoneal kaempferol was administered for 12 days. The Morris water maze (MWM) was used to measure learning and memory performance in the rats, and proteins related to memory formation were investigated in the hippocampi with western blotting. Kaempferol improved learning performance and memory decline in STZ‑treated rats. At the molecular level, STZ‑induced neurodegeneration resulted in a decrease in the expression of GAD67, reelin, and phosphorylated‑NMDAR. However, kaempferol treatment ameliorated these changes by enhancing their levels similar to the controls. While neither STZ injection nor kaempferol treatment produced any significant change in phosphorylated‑CAMKII levels, they increased the expression of klotho and prealbumin. These results show that kaempferol has positive effects on memory loss, affecting synaptic plasticity by ameliorating both the levels and activity of memory‑relevant molecules through reelin signaling. In summary, this study provides a guide to future studies by examining in detail the healing effect of kaempferol as a candidate molecule in the treatment of neurodegeneration, such as that observed in Alzheimer's disease.

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山奈酚治疗通过作用于reelin信号,改善STZ诱导的神经退行性变的记忆障碍。
许多治疗举措,如草药产品及其活性成分,旨在缓解神经退行性变,提高认知功能。山奈酚可能是治疗神经退行性变的候选分子,因为它具有抗氧化作用。在本研究中,我们检测了山奈酚对链脲佐菌素(STZ)诱导的神经退行性变的记忆增强作用相关的分子变化。Long‑Evans雄性大鼠侧脑室注射STZ后,腹腔注射山奈酚12天。用Morris水迷宫(MWM)测定大鼠的学习记忆能力,并用蛋白质印迹法研究海马中与记忆形成有关的蛋白质。山奈酚改善了STZ治疗大鼠的学习成绩和记忆力下降。在分子水平上,STZ诱导的神经退行性变导致GAD67、reelin和磷酸化NMDAR的表达减少。然而,山奈酚治疗通过提高与对照组相似的水平来改善这些变化。虽然STZ注射和山奈酚治疗都没有对磷酸化的‑CAMKII水平产生任何显著变化,但它们增加了klotho和前白蛋白的表达。这些结果表明,山奈酚对记忆丧失有积极影响,通过reelin信号改善记忆相关分子的水平和活性,从而影响突触可塑性。总之,这项研究通过详细检查山奈酚作为候选分子在治疗神经退行性变(如阿尔茨海默病)中的愈合作用,为未来的研究提供了指导。
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来源期刊
CiteScore
2.20
自引率
7.10%
发文量
40
审稿时长
>12 weeks
期刊介绍: Acta Neurobiologiae Experimentalis (ISSN: 0065-1400 (print), eISSN: 1689-0035) covers all aspects of neuroscience, from molecular and cellular neurobiology of the nervous system, through cellular and systems electrophysiology, brain imaging, functional and comparative neuroanatomy, development and evolution of the nervous system, behavior and neuropsychology to brain aging and pathology, including neuroinformatics and modeling.
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