Mitochondrial-derived peptides in cardiovascular disease: Novel insights and therapeutic opportunities.
Li. Yang Y; Li. Zhuozhuo Z; Ren. Yuanyuan Y; Lei. Ying Y; Yang. Silong S; Shi. Yuqi Y; Peng. Han H; Yang. Weijie W; Guo. Tiantian T; Yu. Yi Y; Xiong. Yuyan Y
Key Findings
- Mitochondrial‑derived peptides (including humanin) regulate apoptosis, inflammation, and oxidative stress
- Humanin and related peptides decline with aging and cardiovascular disease, making them potential biomarkers
- Pre‑clinical data suggest these peptides could be therapeutic targets for heart disease, but human trials are still early
Practical Outcomes
- For biohackers, the main takeaway is that boosting or preserving humanin levels might support heart health, but there’s no proven supplement protocol yet. Keep an eye on emerging clinical trials and consider lifestyle strategies that support mitochondrial health, such as regular exercise, adequate sleep, and possibly nutraceuticals that enhance mitochondrial function.
Summary
This review explains that tiny proteins made by mitochondria, like humanin, help control cell death, inflammation, and oxidative stress. Their levels drop as we age and when heart disease is present, so they could serve as early warning signals and maybe even be used as treatments, but the paper doesn’t give specific ways to use them yet.
Abstract
Mitochondria-derived peptides (MDPs) represent a recently discovered family of peptides encoded by short open reading frames (ORFs) found within mitochondrial genes. This group includes notable members including humanin (HN), mitochondrial ORF of the 12S rDNA type-c (MOTS-c), and small humanin-like peptides 1-6 (SHLP1-6). MDPs assume pivotal roles in the regulation of diverse cellular processes, encompassing apoptosis, inflammation, and oxidative stress, which are all essential for sustaining cellular viability and normal physiological functions. Their emerging significance extends beyond this, prompting a deeper exploration into their multifaceted roles and potential applications. This review aims to comprehensively explore the biogenesis, various types, and diverse functions of MDPs. It seeks to elucidate the central roles and underlying mechanisms by which MDPs participate in the onset and development of cardiovascular diseases (CVDs), bridging the connections between cell apoptosis, inflammation, and oxidative stress. Furthermore, the review highlights recent advancements in clinical research related to the utilization of MDPs in CVD diagnosis and treatment. MDPs levels are diminished with aging and in the presence of CVDs, rendering them potential new indicators for the diagnosis of CVDs. Also, MDPs may represent a novel and promising strategy for CVD therapy. In this review, we delve into the biogenesis, various types, and diverse functions of MDPs. We aim to shed light on the pivotal roles and the underlying mechanisms through which MDPs contribute to the onset and advancement of CVDs connecting cell apoptosis, inflammation, and oxidative stress. We also provide insights into the current advancements in clinical research related to the utilization of MDPs in the treatment of CVDs. This review may provide valuable information with MDPs for CVD diagnosis and treatment.
Study Information
pubmed
2023
2023-11-24T00:00:00.000Z
10.1016/j.jare.2023.11.018
24
152