Natrus Larysa, Osadchuk Yuliia, Lisakovska Olha, Roch Toralf, Babel Nina, Klys Yuliia, Labudzynskyi Dmytro, Chaikovsky Yuri
Department of Modern Technologies of Medical Diagnostics & Treatment, Bogomolets National Medical University, 34 Peremoha Avenue, Kyiv 03115, Ukraine.
Department of Histology and Embryology, Bogomolets National Medical University, 34 Peremoha Avenue, Kyiv 03115, Ukraine.
Heliyon. 2022 Nov 14;8(11):e11529. doi: 10.1016/j.heliyon.2022.e11529. eCollection 2022 Nov.
Hypothalamic dysregulation may cause abnormal glucose metabolism and type 2 diabetes mellitus (T2DM). The balance between autophagy and apoptosis is important for maintaining cellular/tissue homeostasis and may be disrupted in T2DM.
Since propionic acid (PA) exerts neuroprotective effects, the aim was to investigate its effects on apoptosis/autophagy switch in the ventromedial hypothalamus (VMH) of T2DM rats.
Male Wistar rats were divided: 1) control; 2) T2DM; groups that received (14 days, orally): 3) metformin (60 mg/kg); 4) sodium salt of PA (60 mg/kg); 5) PA + metformin. Western blotting (Bax, Bcl-xl, LC3, Beclin-1, caspase-3), RT-PCR (Bax, Bcl-xl, LC3, Beclin-1), transmission electron microscopy and immunohistochemical staining (Bax, Bcl-xl) were performed on the VMH samples.
T2DM-induced apoptosis and mitoptosis, enlarged endoplasmic reticulum (ER) tubules/cisterns were observed in VMH, and accompanied by an imbalance of pro- and anti-apoptotic factors: elevation of pro-apoptotic markers Bax and caspase-3, decrease in autophagy protein LC3 and anti-apoptotic Bcl-xl. Metformin and PA administration partially improved VMH ultrastructural changes by reducing mitochondrial swelling and diminishing the number of apoptotic neurons. Metformin inhibited neuronal apoptosis, however, caused reactive astrogliosis and accumulation of lipofuscin granules. Elevated number of autophagosomes was associated with the LC3, Beclin-1 and Bcl-xl increase and decrease in Bax and caspase-3 vs. T2DM. PA switched cell fate from apoptosis to autophagy by elevating LC3 and Beclin-1 levels, increasing Bcl-xl content that altogether may represent adaptive response to T2DM-induced apoptosis. PA + metformin administration lowered relative area of ER membranes/cisterns vs. control, T2DM and metformin, and was optimal considering ratio between the pro-apoptotic, anti-apoptotic and autophagy markers.
T2DM was associated with apoptosis activation leading to impairments in VMH. PA in combination with metformin may be effective against diabetes-induced cell death by switching apoptosis to autophagy in VMH.
下丘脑功能失调可能导致葡萄糖代谢异常及2型糖尿病(T2DM)。自噬与凋亡之间的平衡对于维持细胞/组织稳态至关重要,而在T2DM中可能会被破坏。
鉴于丙酸(PA)具有神经保护作用,本研究旨在探讨其对T2DM大鼠腹内侧下丘脑(VMH)中凋亡/自噬转换的影响。
将雄性Wistar大鼠分为:1)对照组;2)T2DM组;给药组(口服14天):3)二甲双胍(60 mg/kg);4)PA钠盐(60 mg/kg);5)PA + 二甲双胍。对VMH样本进行蛋白质免疫印迹法(检测Bax、Bcl-xl、LC3、Beclin-1、caspase-3)、逆转录聚合酶链反应(检测Bax、Bcl-xl、LC3、Beclin-1)、透射电子显微镜检查及免疫组织化学染色(检测Bax和Bcl-xl)。
在VMH中观察到T2DM诱导的凋亡和有丝分裂性细胞死亡、内质网(ER)小管/池扩大,同时伴有促凋亡和抗凋亡因子失衡:促凋亡标志物Bax和caspase-3升高,自噬蛋白LC3和抗凋亡蛋白Bcl-xl降低。二甲双胍和PA给药通过减轻线粒体肿胀和减少凋亡神经元数量部分改善了VMH超微结构变化。二甲双胍抑制神经元凋亡,但导致反应性星形胶质细胞增生和脂褐素颗粒积累。与T2DM相比,自噬体数量增加与LC3、Beclin-1和Bcl-xl升高以及Bax和caspase-3降低有关。PA通过提高LC3和Beclin-1水平、增加Bcl-xl含量将细胞命运从凋亡转换为自噬,这可能共同代表了对T2DM诱导的凋亡的适应性反应。与对照组、T2DM组和二甲双胍组相比,PA + 二甲双胍给药降低了ER膜/池的相对面积,并且在促凋亡、抗凋亡和自噬标志物之间的比例方面是最佳的。
T2DM与导致VMH损伤的凋亡激活有关。PA与二甲双胍联合使用可能通过将VMH中的凋亡转换为自噬有效对抗糖尿病诱导的细胞死亡。