Wirth Galina, Juusola Greta, Laakso Hanne, Laham-Karam Nihay, Ylä-Herttuala Seppo, Korpisalo Petra
Heart Center, Kuopio University Hospital, Kuopio, Finland.
A. I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, Kuopio, Finland.
Front Bioeng Biotechnol. 2025 May 27;13:1512962. doi: 10.3389/fbioe.2025.1512962. eCollection 2025.
Hyperlipidemia is known to impair endothelial function. We have recently shown that hyperlipidemia also blunts native post-ischemic capillary enlargement that is important for efficient skeletal muscle recovery from ischemia as it supports the recovery of arterial driving pressure and through intussusception increases capillary density. The correction of capillary reactivity under hyperlipidemia could, therefore, improve post-ischemic skeletal muscle recovery. This study tested the ability of adenoviral (Ad) vascular endothelial growth factor (VEGF) gene therapy to rescue capillary enlargement and improve post-ischemic muscle repair in hyperlipidemic mice.
AdVEGF or AdLacZ-control vector were delivered into the calf muscles of aged, hyperlipidemic LDLRApoB mice (n = 58) after induction of acute ischemia. The effects of AdVEGF on capillary phenotype, tissue edema, restoration of blood flow parameters, microvascular hemoglobin oxygenation and tissue damage/regeneration were evaluated using immunohistological analyses, magnetic resonance imaging, contrast-enhanced ultrasound imaging, photoacoustic imaging and histological analyses, respectively, up to 29 days after induced ischemia and gene transfer.
It was found that AdVEGF gene therapy was able to promote capillary enlargement (P < 0.05) that led to recovery of arterial driving pressure in ischemic LDLRApoB muscles. However, capillary enlargement induced by AdVEGF in the hyperlipidemic mice was delayed, had a long-lasting effect (P < 0.05) and did not promote intussusception. Instead, side-effects of VEGF-induced capillary enlargement, i.e., tissue edema (P < 0.01) and subsequently delayed blood flow recovery (P < 0.05), aggravated ischemic tissue damage (P < 0.01).
Hyperlipidemia or old age did not seem to impair AdVEGF-induced capillary enlargement. However, regarding the side-effects of capillary enlargement, therapies trying to promote post-ischemic skeletal muscle recovery through angiogenesis should consider not only capillary size or density but also timing and dynamics of the capillary changes.
已知高脂血症会损害内皮功能。我们最近发现,高脂血症还会抑制缺血后天然毛细血管的扩张,而这种扩张对骨骼肌从缺血中有效恢复很重要,因为它有助于恢复动脉驱动压,并通过套叠增加毛细血管密度。因此,纠正高脂血症状态下的毛细血管反应性可能会改善缺血后骨骼肌的恢复。本研究测试了腺病毒(Ad)血管内皮生长因子(VEGF)基因治疗挽救高脂血症小鼠毛细血管扩张并改善缺血后肌肉修复的能力。
在诱导急性缺血后,将AdVEGF或AdLacZ对照载体注射到老年高脂血症LDLRApoB小鼠(n = 58)的小腿肌肉中。分别使用免疫组织学分析、磁共振成像、对比增强超声成像、光声成像和组织学分析,评估AdVEGF对毛细血管表型、组织水肿、血流参数恢复、微血管血红蛋白氧合以及组织损伤/再生的影响,直至缺血和基因转移后29天。
发现AdVEGF基因治疗能够促进毛细血管扩张(P < 0.05),从而使缺血的LDLRApoB肌肉中的动脉驱动压恢复。然而,AdVEGF在高脂血症小鼠中诱导的毛细血管扩张延迟,具有持久效应(P < 0.05),且不促进套叠。相反,VEGF诱导的毛细血管扩张的副作用,即组织水肿(P < 0.01)以及随后延迟的血流恢复(P < 0.05),加重了缺血组织损伤(P < 0.01)。
高脂血症或衰老似乎并未损害AdVEGF诱导的毛细血管扩张。然而,考虑到毛细血管扩张的副作用,试图通过血管生成促进缺血后骨骼肌恢复的治疗不仅应考虑毛细血管的大小或密度,还应考虑毛细血管变化的时间和动态。