Division of Neuroscience, Faculty of Biology, Medicine & Health, School of Biological Science, The University of Manchester, 3.540 Stopford Building, Oxford Road, Manchester M13 9PT, UK.
Int J Mol Sci. 2024 Sep 23;25(18):10205. doi: 10.3390/ijms251810205.
Cerebrospinal fluid (CSF) is a fluid critical to brain development, function, and health. It is actively secreted by the choroid plexus, and it emanates from brain tissue due to osmolar exchange and the constant contribution of brain metabolism and astroglial fluid output to interstitial fluid into the ventricles of the brain. CSF acts as a growth medium for the developing cerebral cortex and a source of nutrients and signalling throughout life. Together with perivascular glymphatic and interstitial fluid movement through the brain and into CSF, it also acts to remove toxins and maintain metabolic balance. In this study, we focused on cerebral folate status, measuring CSF concentrations of folate receptor alpha (FOLR1); aldehyde dehydrogenase 1L1, also known as 10-formyl tetrahydrofolate dehydrogenase (ALDH1L1 and FDH); and total folate. These demonstrate the transport of folate from blood across the blood-CSF barrier and into CSF (FOLR1 + folate), and the transport of folate through the primary FDH pathway from CSF into brain FDH + ve astrocytes. Based on our hypothesis that CSF flow, drainage issues, or osmotic forces, resulting in fluid accumulation, would have an associated cerebral folate imbalance, we investigated folate status in CSF from neurological conditions that have a severity association with enlarged ventricles. We found that all the conditions we examined had a folate imbalance, but these folate imbalances were not all the same. Given that folate is essential for key cellular processes, including DNA/RNA synthesis, methylation, nitric oxide, and neurotransmitter synthesis, we conclude that ageing or some form of trauma in life can lead to CSF accumulation and ventricular enlargement and result in a specific folate imbalance/deficiency associated with the specific neurological condition. We believe that addressing cerebral folate imbalance may therefore alleviate many of the underlying deficits and symptoms in these conditions.
脑脊液(CSF)是对大脑发育、功能和健康至关重要的液体。它由脉络丛主动分泌,由于渗透压交换以及大脑代谢和星形胶质细胞液体输出不断向脑间质液进入脑室,CSF 从脑组织中逸出。CSF 充当发育中的大脑皮层的生长培养基,并在整个生命周期中为营养物质和信号提供来源。与脑内血管周围的神经胶质淋巴和间质液通过大脑并进入 CSF 的运动一起,它还有助于清除毒素并维持代谢平衡。在这项研究中,我们专注于大脑叶酸状态,测量 CSF 中叶酸受体 alpha(FOLR1);醛脱氢酶 1L1,也称为 10-甲酰四氢叶酸脱氢酶(ALDH1L1 和 FDH);以及总叶酸。这些表明叶酸从血液穿过血脑屏障进入 CSF(FOLR1+叶酸)的转运,以及叶酸通过 CSF 进入脑 FDH+ve 星形胶质细胞的主要 FDH 途径的转运。基于我们的假设,即 CSF 流动、引流问题或渗透压导致液体积聚,会导致相关的大脑叶酸失衡,我们研究了与脑室扩大严重程度相关的神经状况下 CSF 中的叶酸状态。我们发现,我们检查的所有情况都存在叶酸失衡,但这些叶酸失衡并不完全相同。鉴于叶酸对包括 DNA/RNA 合成、甲基化、一氧化氮和神经递质合成在内的关键细胞过程至关重要,我们得出结论,衰老或生活中的某种创伤会导致 CSF 积聚和脑室扩大,并导致与特定神经状况相关的特定叶酸失衡/缺乏。我们认为,解决大脑叶酸失衡可能会缓解这些情况下的许多潜在缺陷和症状。