Tsoi Shuk C, Barrientos Alicia C, Vicario David S, Phan Mimi L, Pytte Carolyn L
CUNY Neuroscience Collaborative, Psychology and Biology Departments, The Graduate Center, City University of New York, New York, New York, United States of America.
Department of Psychology, Rutgers, The State University of New Jersey, Piscataway, New Jersey, United States of America.
PLoS One. 2025 Apr 28;20(4):e0314690. doi: 10.1371/journal.pone.0314690. eCollection 2025.
Statins are highly effective and widely prescribed cholesterol lowering drugs. However, statins cross the blood-brain barrier and decrease neural cholesterol in animal models, raising concern that long-term statin use may impact cholesterol-dependent structures and functions in the brain. Cholesterol is a fundamental component of cell membranes and experimentally decreasing membrane cholesterol has been shown to alter cell morphology in vitro. In addition, brain regions that undergo adult neurogenesis rely on local brain cholesterol for the manufacture of new neuronal membranes. Thus neurogenesis may be particularly vulnerable to long-term statin use. Here we asked whether oral statin treatment impacts neurogenesis in juveniles, either by decreasing numbers of new cells formed or altering the structure of new neurons. The use of statins in children and adolescents has received less attention than in older adults, with few studies on potential unintended effects in young brains. We examined neurons in the juvenile zebra finch songbird in telencephalic regions that function in song perception and memory (caudomedial nidopallium, NCM) and song production (HVC). Birds received either 40 mg/kg of atorvastatin in water or water vehicle once daily for 2-3 months until they reached adulthood. We labeled newborn cells using systemic injections of bromodeoxyuridine (BrdU) and quantified cells double-labeled with antibodies for BrdU and the neuron-specific protein Hu 30-32 days post mitosis. We also quantified a younger cohort of new neurons in the same birds using antibody to the neuronal protein doublecortin (DCX). We then compared numbers of new neurons and soma morphology of BrdU + /Hu+ neurons between statin-treated and control birds. We did not find an effect of statins on the density of newly formed neurons in either brain region, suggesting that statin treatment did not impact neurogenesis or young neuron survival in our paradigm. However, we found that neuronal soma morphology differed significantly between statin-treated and control birds. Somata of BrdU + /Hu+ (30-32 day old) neurons were flatter and had more furrowed contours in statin-treated birds relative to controls. In a larger, heterogeneous cohort of non-birthdated BrdU-/Hu+ neurons, largely born prior to statin treatment, somata were smaller in statin-treated birds than in controls. Our findings indicate that atorvastatin may affect neural cytoarchitecture in both newly formed and mature neurons, perhaps as a consequence of decreased cholesterol availability in the brain.
他汀类药物是非常有效的降胆固醇药物,被广泛应用于临床治疗。然而,在动物模型中,他汀类药物能够穿过血脑屏障并降低神经胆固醇水平,这引发了人们对长期使用他汀类药物可能影响大脑中依赖胆固醇的结构和功能的担忧。胆固醇是细胞膜的基本组成成分,实验表明,在体外降低膜胆固醇会改变细胞形态。此外,经历成年神经发生的脑区依赖局部脑胆固醇来制造新的神经元膜。因此,神经发生可能特别容易受到长期使用他汀类药物的影响。在这里,我们研究口服他汀类药物治疗是否会影响幼鸟的神经发生,无论是通过减少新形成细胞的数量还是改变新神经元的结构。与老年人相比,儿童和青少年使用他汀类药物受到的关注较少,关于对幼鸟潜在意外影响的研究也很少。我们在斑胸草雀幼鸟的端脑区域检查了神经元,这些区域在歌曲感知和记忆(内侧巢皮质,NCM)以及歌曲产生(HVC)中发挥作用。鸟类每天一次在水中接受40mg/kg的阿托伐他汀或仅接受水载体,持续2 - 3个月,直到成年。我们通过全身注射溴脱氧尿苷(BrdU)标记新生细胞,并在有丝分裂后30 - 32天用针对BrdU和神经元特异性蛋白Hu的抗体对细胞进行双标记定量。我们还用针对神经元蛋白双皮质素(DCX)的抗体对同一批鸟类中较年轻的新生神经元群体进行了定量。然后,我们比较了他汀类药物治疗组和对照组鸟类中新生神经元的数量以及BrdU+/Hu+神经元的体细胞形态。我们没有发现他汀类药物对任何一个脑区新形成神经元的密度有影响,这表明在我们的实验范式中,他汀类药物治疗没有影响神经发生或年轻神经元的存活。然而,我们发现他汀类药物治疗组和对照组鸟类的神经元体细胞形态存在显著差异。相对于对照组,他汀类药物治疗组中BrdU+/Hu+(30 - 32天大)神经元的体细胞更扁平,轮廓更有褶皱。在一个更大的、异质性的未标记出生时间的BrdU-/Hu+神经元群体中,这些神经元大多在他汀类药物治疗之前出生,他汀类药物治疗组的体细胞比对照组小。我们的研究结果表明,阿托伐他汀可能会影响新形成和成熟神经元的神经细胞结构,这可能是由于大脑中胆固醇供应减少所致。