Shin Seulgi, Jo Hyejung, Agura Tomoyo, Jeong Seoyoun, Ahn Hyovin, Pang Soyoung, Lee June, Park Jeong-Ho, Kim Yejin, Kang Jae Seung
Laboratory of Vitamin C and Antioxidant Immunology, Department of Anatomy and Cell Biology, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.
Institute of Allergy and Clinical Immunology, Seoul National University Medical Research Center, Seoul 08826, Republic of Korea.
Pharmaceuticals (Basel). 2024 Nov 24;17(12):1577. doi: 10.3390/ph17121577.
: Vitamin C is a well-known antioxidant with antiviral, anticancer, and anti-inflammatory properties. However, its therapeutic applications are limited by rapid oxidation due to heat and light sensitivity. Aptamin C, which employs aptamers to bind vitamin C, has demonstrated enhanced stability and efficacy. This study investigates the potential of Aptamin C to inhibit the progression of pulmonary fibrosis, a prominent inflammatory lung disease with no effective treatment. : Mice bearing bleomycin-induced pulmonary fibrosis were administered vitamin C or Aptamin C, and their weight changes and survival rates were monitored. Inflammatory cell infiltration was assessed in the bronchoalveolar lavage fluid (BALF), and the degree of alveolar fibrosis was measured by H&E and Masson's trichrome staining. To elucidate the mechanism of action of Aptamin C, Western blot analysis was performed in HaCaT and lung tissues from bleomycin-induced pulmonary fibrosis mice. : The Aptamin C-treated group showed a notably higher survival rate at 50%, whereas all subjects in the vitamin C-treated group died. Histological examination of lung tissue showed that inflammation was significantly suppressed in the Aptamin C-supplemented group compared to the vitamin C-supplemented group, with a 10% greater reduction in cell infiltrations, along with noticeably less tissue damage. Additionally, it was observed that Aptamin C increased SVCT-1 expression in the HaCaT cells and the lung tissues. : Taken together, Aptamin C not only increases the stability of vitamin C but also induces an increase in SVCT-1 expression, facilitating greater vitamin C absorption into cells and tissues, thereby inhibiting the progression of symptoms and associated inflammatory responses in pulmonary fibrosis.
维生素C是一种著名的抗氧化剂,具有抗病毒、抗癌和抗炎特性。然而,由于其对热和光敏感,会迅速氧化,限制了其治疗应用。Aptamin C利用适配体与维生素C结合,已证明具有更高的稳定性和疗效。本研究调查了Aptamin C抑制肺纤维化进展的潜力,肺纤维化是一种突出的炎症性肺病,目前尚无有效治疗方法。
对博来霉素诱导的肺纤维化小鼠给予维生素C或Aptamin C,并监测其体重变化和存活率。评估支气管肺泡灌洗液(BALF)中的炎性细胞浸润情况,通过苏木精-伊红(H&E)染色和马松三色染色测量肺泡纤维化程度。为阐明Aptamin C的作用机制,对HaCaT细胞和博来霉素诱导的肺纤维化小鼠的肺组织进行蛋白质印迹分析。
Aptamin C治疗组的存活率显著更高,为50%,而维生素C治疗组的所有小鼠均死亡。肺组织的组织学检查表明,与补充维生素C的组相比,补充Aptamin C的组炎症得到显著抑制,细胞浸润减少10%,组织损伤也明显减轻。此外,观察到Aptamin C增加了HaCaT细胞和肺组织中SVCT-1的表达。
综上所述,Aptamin C不仅提高了维生素C的稳定性,还诱导了SVCT-1表达的增加,促进更多的维生素C吸收到细胞和组织中,从而抑制肺纤维化症状的进展及相关炎症反应。