Boison Detlev
RS Dow Neurobiology Labs, Legacy Research Institute, Portland OR
Adenosine is an endogenous anticonvulsant that is controlled by an astrocyte-based adenosine cycle and expression levels of its key negative regulator adenosine kinase (ADK). Astrogliosis, a pathological hallmark of the epileptic brain, is universally accompanied by overexpression of ADK and resulting adenosine deficiency. Thereby deregulated ADK provides a molecular link between astrogliosis and neuronal dysfunction in epilepsy. Since overexpression of ADK and resulting adenosine deficiency are sufficient to initiate spontaneous recurrent seizures, focal adenosine augmentation therapies (AATs) constitute a rational approach for the suppression and prevention of seizures. Systemic pharmacological AATs using either ADK inhibitors or adenosine A receptor agonists are effective in seizure suppression, however accompanied by wide-spread, largely cardiovascular, side-effects that can only be avoided via focal delivery approaches. As therapeutic tools to achieve focal AAT, stem cells have been engineered to release therapeutic amounts of adenosine using RNA interference or gene targeting technology. In rodent models, stem cell-derived brain-implants provide robust protection from induced and spontaneous seizures through the paracrine delivery of adenosine. Most recently, silk-based polymers have been bioengineered to release adenosine with the goal to translate focal AATs into clinical applications.
腺苷是一种内源性抗惊厥剂,受基于星形胶质细胞的腺苷循环及其关键负调节因子腺苷激酶(ADK)的表达水平控制。星形胶质细胞增生是癫痫脑的一个病理标志,普遍伴有ADK的过度表达和由此导致的腺苷缺乏。因此,失调的ADK在癫痫中提供了星形胶质细胞增生与神经元功能障碍之间的分子联系。由于ADK的过度表达和由此导致的腺苷缺乏足以引发自发性反复癫痫发作,局部腺苷增强疗法(AATs)构成了一种抑制和预防癫痫发作的合理方法。使用ADK抑制剂或腺苷A受体激动剂的全身性药理AATs在癫痫发作抑制方面有效,然而伴有广泛的、主要是心血管方面的副作用,这些副作用只能通过局部递送方法来避免。作为实现局部AAT的治疗工具,干细胞已被设计利用RNA干扰或基因靶向技术释放治疗量的腺苷。在啮齿动物模型中,干细胞衍生的脑植入物通过旁分泌递送腺苷,为诱导性和自发性癫痫发作提供了强大的保护。最近,基于丝的聚合物已被生物工程改造以释放腺苷,目的是将局部AATs转化为临床应用。