Daily oral administration of probiotics engineered to constantly secrete short-chain fatty acids effectively prevents myocardial injury from subsequent ischaemic heart disease.

IF 10.2 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiovascular Research Pub Date : 2024-11-25 DOI:10.1093/cvr/cvae128
Quynh Hoa Pham, Thi Van Anh Bui, Woo-Sup Sim, King Hoo Lim, Carmen Oi Kwan Law, Wanyu Tan, Ri Youn Kim, Kwan Ting Chow, Hun-Jun Park, Kiwon Ban, Terrence Chi Kong Lau
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Abstract

Aims: Given the extremely limited regeneration potential of the heart, one of the most effective strategies to reduce the prevalence and mortality of coronary artery disease is prevention. Short-chain fatty acids (SCFAs), which are by-products of beneficial probiotics, have been reported to possess cardioprotective effects. Despite their beneficial roles, delivering SCFAs and maintaining their effective concentration in plasma present major challenges. Therefore, in the present study, we aimed to devise a strategy to prevent coronary heart disease effectively by using engineered probiotics to continuously release SCFAs in vivo.

Methods and results: We engineered a novel probiotic cocktail, namely EcN_TL, from the commercially available Escherichia coli Nissle 1917 (EcN) strain to continuously secrete SCFAs by introducing the propionate and butyrate biosynthetic pathways. Oral administration of EcN_TL enhanced and maintained an effective concentration of SCFAs in the plasma. As a preventative strategy, we observed that daily intake of EcN_TL for 14 days prior to ischaemia-reperfusion injury significantly reduced myocardial injury and improved cardiac performance compared with EcN administration. We uncovered that EcN_TL's protective mechanisms included reducing neutrophil infiltration into the infarct site and promoting the polarization of wound healing macrophages. We further revealed that SCFAs at plasma concentration protected cardiomyocytes from inflammation by suppressing the NF-κB activation pathway.

Conclusion: These data provide strong evidence to support the use of SCFA-secreting probiotics to prevent coronary heart disease. Since SCFAs also play a key role in other metabolic diseases, EcN_TL can potentially be used to treat a variety of other diseases.

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每天口服能持续分泌短链脂肪酸的益生菌,能有效预防缺血性心脏病造成的心肌损伤。
目的:鉴于心脏的再生能力极为有限,降低冠心病发病率和死亡率的最有效策略之一就是预防。据报道,有益益生菌的副产品--短链脂肪酸(SCFAs)具有保护心脏的作用。尽管短链脂肪酸对人体有益,但如何输送短链脂肪酸并保持其在血浆中的有效浓度却是一大挑战。因此,在本研究中,我们旨在设计一种策略,利用工程益生菌在体内持续释放 SCFAs,从而有效预防冠心病:我们从市售的大肠杆菌 Nissle 1917 菌株中引入丙酸盐和丁酸盐生物合成途径,设计出一种新型鸡尾酒益生菌 EcN_TL,可持续分泌 SCFAs。口服 EcN_TL 可提高并维持血浆中 SCFAs 的有效浓度。作为一种预防性策略,我们观察到,与服用 EcN 相比,在缺血再灌注损伤前 14 天每天服用 EcN_TL 可显著减轻心肌损伤并改善心脏性能。我们发现,EcN_TL 的保护机制包括减少中性粒细胞向梗死部位的浸润和促进伤口愈合巨噬细胞的极化。我们进一步发现,血浆浓度的 SCFAs 可通过抑制 NF-κB 激活途径保护心肌细胞免受炎症侵袭:这些数据为使用分泌 SCFA 的益生菌预防冠心病提供了强有力的证据。由于 SCFAs 在其他代谢性疾病中也起着关键作用,EcN_TL 有可能被用于治疗其他各种疾病。
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来源期刊
Cardiovascular Research
Cardiovascular Research 医学-心血管系统
CiteScore
21.50
自引率
3.70%
发文量
547
审稿时长
1 months
期刊介绍: Cardiovascular Research Journal Overview: International journal of the European Society of Cardiology Focuses on basic and translational research in cardiology and cardiovascular biology Aims to enhance insight into cardiovascular disease mechanisms and innovation prospects Submission Criteria: Welcomes papers covering molecular, sub-cellular, cellular, organ, and organism levels Accepts clinical proof-of-concept and translational studies Manuscripts expected to provide significant contribution to cardiovascular biology and diseases
期刊最新文献
Daily oral administration of probiotics engineered to constantly secrete short-chain fatty acids effectively prevents myocardial injury from subsequent ischaemic heart disease. Corrigendum to: Clinical Case 29-The role of transthoracic echocardiography on patients presenting with shock of unknown etiology. Corrigendum to: Lamin: Guardian against DNA damage by transcription stress. Cross-species single-cell RNA sequencing reveals divergent phenotypes and activation states of adaptive immunity in human carotid and experimental murine atherosclerosis. Crucial role for sensory nerves and Na/H exchanger inhibition in dapagliflozin- and empagliflozin-induced arterial relaxation.
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