受淀粉样蛋白-β影响的Ca2+振荡的数字化实现

Mahsasadat Seyedbarhagh, A. Ahmadi, M. Ahmadi
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引用次数: 1

摘要

细胞内Ca2+动态的任何失调与β淀粉样蛋白(Aβ)斑块的异常积累都可以引起神经炎症,从而导致阿尔茨海默病(AD)的发展。本文根据IP3受体(IPR)、质膜泵、肌内质网Ca2+ atp酶(SERCA)泵、ryanodine受体通道和一般膜泄漏等生物计算模型,采用坐标旋转数字计算机(CORDIC)算法进行了无乘法器的数字设计。硬件实现和数值分析表明,基于cordic的细胞内Ca2+动力学可以模拟细胞内Ca2+的相同生化行为,差异可以忽略不计。
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Digital Realization of Ca2+ Oscillation With Impact of Amyloid-β
Any dysregulation for intracellular Ca2+ dynamic with abnormally accumulation of Amyloid beta (Aβ) plaques can cause neuroinflammation which leads to the development of Alzheimer’s Disease (AD). In this paper, a multiplierless digital design with COordinate Rotation DIgital Computer (CORDIC) algorithm according to a biologically computational model including IP3 receptors (IPR), plasma membrane pump, a sarco-endoplasmic reticulum Ca2+ ATPase (SERCA) pump, ryanodine receptors channels, and general membrane leak is represented. Hardware implementation and the numerical analysis illustrates that, the CORDIC-based intracellular Ca2+ dynamics can emulate the same biochemical behavior of the Ca2+ in cells with negligible variance.
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