A Polyunsaturated Fatty Acid (PUFA) Theory of Schizophrenia

Ari Rappoport
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Abstract

I present a theory of schizophrenia (SZ) that mechanistically explains its etiology, symptoms, pathophysiology, and treatment. SZ involves the chronic release of membrane polyunsaturated fatty acids (PUFAs) and their utilization for the synthesis of stress-induced plasticity agents such as endocannabinoids (ECBs). The causal event in SZ is prolonged stress during a sensitive period, which can induce prolonged and heritable changes. The physiological effect of the released PUFAs and their products is to disconnect neurons from their inputs and promote intrinsic excitability. I show that these effects can explain the positive, negative, cognitive, and mood symptoms of SZ, as well as the mechanisms of many known triggers of psychosis. The theory is supported by overwhelming evidence addressing lipids, immunity, ECBs, neuromodulators, hormones, neurotransmitters, and cortical parameters in SZ. It explains why antipsychotic drugs are effective against positive symptoms, and why they do not affect the other symptoms. Finally, I present promising treatment directions implied by the theory, including some that are immediately available.
精神分裂症的多不饱和脂肪酸 (PUFA) 理论
我提出的精神分裂症(SZ)理论从机理上解释了精神分裂症的病因、症状、病理生理学和治疗。精神分裂症涉及膜多不饱和脂肪酸(PUFAs)的慢性释放及其用于合成应激诱导的可塑性物质(如内源性大麻素(ECBs))。SZ 的致病因素是敏感期内的长期应激,这种应激可诱发长期的遗传性变化。释放的 PUFAs 及其产物的生理效应是切断神经元与其输入的联系,并促进内在兴奋性。我的研究表明,这些效应可以解释 SZ 的积极、消极、认知和情绪症状,以及许多已知的精神病诱因的机制。这一理论得到了大量证据的支持,这些证据涉及 SZ 中的血脂、免疫、ECB、神经调节剂、激素、神经递质和皮质参数。它解释了为什么抗精神病药物对阳性症状有效,而对其他症状无效。最后,我介绍了该理论所隐含的有希望的治疗方向,包括一些立即可用的治疗方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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