首页> 美国卫生研究院文献>Brain Sciences >Hypothesis: Astrocyte Foot Processes Detachment from the Neurovascular Unit in Female Diabetic Mice May Impair Modulation of Information Processing—Six Degrees of Separation
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Hypothesis: Astrocyte Foot Processes Detachment from the Neurovascular Unit in Female Diabetic Mice May Impair Modulation of Information Processing—Six Degrees of Separation

机译:假设:雌性糖尿病小鼠中神经血管单位的星形胶质细胞足突脱离可能会损害信息处理的调节-六个分离度

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摘要

Astrocytes via their foot processes (ACfp) are specialized connecting cells, and they structurally connect the neurovascular unit (NVU) mural cells to neurons. Astrocytes provide homeostatic mechanisms for structural connections and provide communication between the NVU and regional neurons for functional hyperemia in regions of increased neuronal activity (neurovascular coupling). Previously, our group has demonstrated a detachment, separation, and retraction of ACfp in diabetic db/db females (DBC). It was hypothesized that a loss of adherent ACfp/NVU could result in the known impaired cognition in DBC. Additionally hypothesized was that empagliflozin treatment could protect DBC ACfp/NVU remodeling. This study demonstrates a significant loss of ACfp/NVU numbers in DBC and a protection of this loss by empagliflozin treatment (DBE). The number of intact ACfp/NVU was 6.45 ± 1.1 in control heterozygous (CKC) vs. 1.88 ± 0.72 in DBC (p < 0.05) and 5.86 ± 0.88 in DBE vs. DBC (p < 0.05) by visually hand-counting the capillary NVUs (22 in CKC, 25 in DBC, and 22 in DBE). These findings suggest that empagliflozin provides neuroprotection via the prevention of ACfp separation in DBE as compared to diabetic DBC. Furthermore, a loss of ACfp/NVU numbers in DBC may correspond with a negative modulation of informational processing, and the protection of ACfp/NVU numbers could provide a protective modulation in DBE models.
机译:星形胶质细胞通过它们的足突(ACfp)是专门的连接细胞,并且它们在结构上将神经血管单位(NVU)壁细胞连接到神经元。星形胶质细胞为结构连接提供了稳态机制,并在神经元活动增加的区域(神经血管耦合)为功能性充血提供了NVU和区域神经元之间的交流。以前,我们的研究组已证明糖尿病性db / db女性(DBC)中ACfp的脱离,分离和收缩。假设丧失附着的ACfp / NVU可能导致已知的DBC认知受损。另外假设是依帕列净治疗可以保护DBC ACfp / NVU重塑。这项研究表明,DBC中ACfp / NVU数量显着减少,并通过恩帕格列净治疗(DBE)来保护这种损失。对照杂合子(CKC)的完整ACfp / NVU数量为6.45±1.1,而DBC与DBC的完整ACfp / NVU数量为1.88±0.72(p <0.05),通过目测毛细血管计数,DBE vs.DBC的完整ACfp / NVU数量为5.86±0.88(p <0.05) NVU(CKC中为22个,DBC中为25个,DBE中为22个)。这些发现表明,与糖尿病性DBC相比,依帕格列净通过防止DBE中ACfp分离提供神经保护作用。此外,DBC中ACfp / NVU编号的丢失可能与信息处理的负调制相对应,并且ACfp / NVU编号的保护可以在DBE模型中提供保护性调制。

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