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新型 RARα 激动剂 BT75 在体外培养小胶质细胞和阿尔茨海默病实验小鼠模型中的抗炎作用。

Anti-inflammatory Action of BT75, a Novel RARα Agonist, in Cultured Microglia and in an Experimental Mouse Model of Alzheimer's Disease.

机构信息

Division of Neurochemistry, Nathan Kline Institute for Psychiatric Research, 140 Old Orangeburg Rd, Orangeburg, NY, 10962, USA.

Emotional Brain Institute, Nathan Kline Institute for Psychiatric Research, Orangeburg, NY, USA.

出版信息

Neurochem Res. 2023 Jun;48(6):1958-1970. doi: 10.1007/s11064-023-03888-x. Epub 2023 Feb 13.

Abstract

BT75, a boron-containing retinoid, is a novel retinoic acid receptor (RAR)α agonist synthesized by our group. Previous studies indicated that activation of retinoic acid (RA) signaling may attenuate progression of Alzheimer's disease (AD). Presently, we aimed to examine the anti-inflammatory effect of BT75 and explore the possible mechanism using cultured cells and an AD mouse model. Pretreatment with BT75 (1-25 µM) suppressed the release of nitric oxide (NO) and IL-1β in the culture medium of mouse microglial SIM-A9 cells activated by LPS. BMS195614, an RARα antagonist, partially blocked the inhibition of NO production by BT75. Moreover, BT75 attenuated phospho-Akt and phospho-NF-κB p65 expression augmented by LPS. In addition, BT75 elevated arginase 1, IL-10, and CD206, and inhibited inducible nitric oxide synthase (iNOS) and IL-6 formation in LPS-treated SIM-A9 cells, suggesting the promotion of M1-M2 microglial phenotypic polarization. C57BL/6 mice were injected intracerebroventricularly (icv) with streptozotocin (STZ) (3 mg/kg) to provide an AD-like mouse model. BT75 (5 mg/kg) or the vehicle was intraperitoneally (ip) injected to icv-STZ mice once a day for 3 weeks. Immunohistochemical analyses indicated that GFAP-positive cells and rod or amoeboid-like Iba1-positive cells, which increased in the hippocampal fimbria of icv-STZ mice, were reduced by BT75 treatment. Western blot results showed that BT75 decreased levels of neuronal nitric oxide synthase (nNOS), GFAP, and phosphorylated Tau, and increased levels of synaptophysin in the hippocampus of icv-STZ mice. BT75 may attenuate neuroinflammation by affecting the Akt/NF-κB pathway and microglial M1-M2 polarization in LPS-stimulated SIM-A9 cells. BT75 also reduced AD-like pathology including glial activation in the icv-STZ mice. Thus, BT75 may be a promising anti-inflammatory and neuroprotective agent worthy of further AD studies.

摘要

BT75 是一种含硼的维甲酸,是本集团合成的新型视黄酸受体 (RAR)α 激动剂。先前的研究表明,激活维甲酸 (RA) 信号可能会减轻阿尔茨海默病 (AD) 的进展。目前,我们旨在使用培养的细胞和 AD 小鼠模型来研究 BT75 的抗炎作用,并探讨其可能的机制。BT75(1-25μM)预处理可抑制 LPS 激活的小鼠小胶质细胞 SIM-A9 细胞培养基中一氧化氮 (NO) 和白细胞介素 1β (IL-1β) 的释放。RARα 拮抗剂 BMS195614 部分阻断了 BT75 对 NO 产生的抑制作用。此外,BT75 减弱了 LPS 增强的磷酸化 Akt 和磷酸化 NF-κB p65 的表达。此外,BT75 升高了 LPS 处理的 SIM-A9 细胞中的精氨酸酶 1、IL-10 和 CD206,并抑制了诱导型一氧化氮合酶 (iNOS) 和 IL-6 的形成,表明促进了 M1-M2 小胶质细胞表型极化。C57BL/6 小鼠通过侧脑室 (icv) 注射链脲佐菌素 (STZ)(3mg/kg)建立 AD 样小鼠模型。BT75(5mg/kg)或载体每天腹腔 (ip) 注射一次,共 3 周。免疫组织化学分析表明,BT75 处理可减少海马弓状纤维中 icv-STZ 小鼠中增加的 GFAP 阳性细胞和杆状或阿米巴样 Iba1 阳性细胞。Western blot 结果表明,BT75 降低了海马神经元型一氧化氮合酶 (nNOS)、GFAP 和磷酸化 Tau 的水平,增加了 icv-STZ 小鼠海马中的突触小体蛋白水平。BT75 通过影响 LPS 刺激的 SIM-A9 细胞中的 Akt/NF-κB 通路和小胶质细胞 M1-M2 极化来减轻神经炎症。BT75 还减少了包括 icv-STZ 小鼠中神经胶质激活在内的 AD 样病理学。因此,BT75 可能是一种有前途的抗炎和神经保护剂,值得进一步研究 AD。

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