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鞘脂激活蛋白原对缺血诱导的学习障碍和神经元损失的保护作用。

Protection by prosaposin against ischemia-induced learning disability and neuronal loss.

作者信息

Sano A, Matsuda S, Wen T C, Kotani Y, Kondoh K, Ueno S, Kakimoto Y, Yoshimura H, Sakanaka M

机构信息

Department of Neuropsychiatry, Ehime University School of Medicine, Japan.

出版信息

Biochem Biophys Res Commun. 1994 Oct 28;204(2):994-1000. doi: 10.1006/bbrc.1994.2558.

Abstract

Prosaposin, the protein precursor of saposins A, B, C, and D which activate sphingolipid hydrolases, is abundant in several brain regions including the hippocampus. We infused prosaposin continuously for 7 days into the lateral ventricle of gerbils starting 3 hours before 3-min of forebrain ischemia. Using the step-down passive avoidance task, we demonstrated that ischemia-induced learning disability is prevented almost completely by prosaposin infusion. Subsequent light and electron microscopic examinations showed that pyramidal neurons in the CA1 field of the hippocampus as well as synapses within the strata moleculare, lacunosum/radiatum and oriens of the field were significantly more numerous in gerbils infused with prosaposin infusion than in those receiving saline infusion. These findings suggest that prosaposin possesses neurotrotrophic activity to protect hippocampal CA1 neurons from lethal ischemic damage.

摘要

前体蛋白原,即激活鞘脂水解酶的鞘脂激活蛋白A、B、C和D的蛋白质前体,在包括海马体在内的几个脑区中含量丰富。我们在沙土鼠前脑缺血3分钟前3小时开始,连续7天向其侧脑室注入前体蛋白原。通过阶梯式被动回避任务,我们证明前体蛋白原注入几乎完全预防了缺血诱导的学习障碍。随后的光镜和电镜检查显示,注入前体蛋白原的沙土鼠海马CA1区的锥体细胞以及该区域分子层、腔隙/辐射层和原层内的突触数量明显多于注入生理盐水的沙土鼠。这些发现表明,前体蛋白原具有神经营养活性,可保护海马CA1神经元免受致命性缺血损伤。

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