Sumneang Natticha, Kobroob Anongporn, Phungphong Sukanya, Boonhoh Worakan, Punsawad Chuchard, Kangwan Napapan
Department of Medical Science, School of Medicine, Walailak University, Nakhon Si Thammarat 80160, Thailand.
Research Center in Tropical Pathobiology, Walailak University, Nakhon Si Thammarat 80160, Thailand.
Nutrients. 2025 Jan 29;17(3):501. doi: 10.3390/nu17030501.
BACKGROUND/OBJECTIVES: Sepsis-induced cardiac dysfunction is a major problem that often leads to severe complications and a poor prognosis. Despite the growing awareness of its impact, effective treatment options for sepsis-induced cardiac dysfunction remain limited. To date, fermented products of (HC), known for its rich bioactive properties, have shown potential in modulating inflammatory and oxidative stress pathways. However, treatment with fermented HC juice (FHJ) in lipopolysaccharide (LPS)-induced sepsis in rats has not been investigated.
Rats were pretreated with FHJ at doses of 200 mg/kg and 400 mg/kg for 2 weeks. After that, the rats were injected with a single dose of LPS (10 mg/kg), and 12 h after injection, they developed sepsis-induced cardiac dysfunction. Then, cardiac function, oxidative stress, inflammation, apoptosis, and cardiac injury markers were determined.
Pretreatment with FHJ at doses of 200 mg/kg and 400 mg/kg prevented LPS-induced cardiac dysfunction in rats by attenuating cardiac inflammation (IL-1β, TLR-4, and NF-κB levels), oxidative stress (MDA levels), and apoptosis (cleaved-caspase 3 and Bax/Bcl-2 expression) and reducing markers of cardiac injury (LDH and CK-MB levels).
These results suggest that FHJ could be a potential therapeutic agent for sepsis-induced heart disease.
背景/目的:脓毒症诱发的心脏功能障碍是一个重大问题,常导致严重并发症及预后不良。尽管人们越来越意识到其影响,但针对脓毒症诱发的心脏功能障碍的有效治疗选择仍然有限。迄今为止,以其丰富的生物活性特性而闻名的(此处原文缺失具体物质名称,假设为HC)发酵产物已显示出调节炎症和氧化应激途径的潜力。然而,发酵的HC汁(FHJ)对脂多糖(LPS)诱导的大鼠脓毒症的治疗作用尚未得到研究。
大鼠分别用200mg/kg和400mg/kg剂量的FHJ预处理2周。之后,给大鼠注射单剂量的LPS(10mg/kg),注射后12小时,它们出现了脓毒症诱发的心脏功能障碍。然后,测定心脏功能、氧化应激、炎症、细胞凋亡和心脏损伤标志物。
200mg/kg和400mg/kg剂量的FHJ预处理通过减轻心脏炎症(IL-1β、TLR-4和NF-κB水平)、氧化应激(MDA水平)和细胞凋亡(裂解的半胱天冬酶3和Bax/Bcl-2表达)以及降低心脏损伤标志物(LDH和CK-MB水平),预防了LPS诱导的大鼠心脏功能障碍。
这些结果表明,FHJ可能是治疗脓毒症诱发心脏病的一种潜在治疗剂。