相关实验视频
Updated: Jun 4, 2025

15:06
Synthesis of an Intein-mediated Artificial Protein Hydrogel
Published on: January 27, 2014
12.1K
深度学习驱动优化乳清蛋白水解剂的抗高血压特性:一种多酶方法
Shuai Jiang1, Fan Mo1, Wenhan Li2
1College of Food Science and Light Industry, Nanjing Tech University, Nanjing 211816, China.
Journal of agricultural and food chemistry
|December 25, 2024
概括
深度学习确定了乳清蛋白中抗高血压的最佳酶组合. 这种新方法显著降低了高血压大鼠的血压和炎症.
科学领域:
- 生物技术是生物技术.
- 营养科学 营养科学
- 计算生物学 计算生物学
背景情况:
- 高血压是一个全球性的健康问题.
- 饮食质为血压管理提供了一个有前途的途径.
- 优化的生产需要先进的方法.
研究的目的:
- 利用深度学习和大型语言模型 (LLM) 来优化乳清蛋白水解剂中的抗高血压.
- 为了评估优化组合的有效性和稳定性.
- 为了研究高血压大鼠模型中作用的潜在机制.
主要方法:
- 使用大型语言模型 (LLM) 来确定最佳的多酶组合 (MC5).
- 通过模拟消化评估了 ангиотензин转化酶 (ACE) 抑制率和生物稳定性.
- 对高血压大鼠进行了体内研究,测量血压,炎症标志物,抗氧化酶和关键血管活性物质.
- 进行分子对接以识别特定的高亲和度结合.
主要成果:
- MC5实现了89.08%的ACE抑制率,显著超过单酶水解.
- MC5表现出极好的生物稳定性,在消化后ACE抑制仅下降6.87%.
- 在体内研究表明,MC5降低了心压和腹压血压,分别为125.00和89.00 mmHg.
- MC5调节了炎症标志物,增强了抗氧化酶活性,并有利地改变了氨酸- ангиотензин-阿尔多斯特系统 (RAAS) 组成部分和氧化 (NO) 水平.
- 通过分子对接识别了四种强大的抗高血压 (LPEW,LKPTPEGDL,LNYW,LLL).
结论:
- 深度学习和LLM是优化化中的酶组合用于抗高血压应用的有效工具.
- 优化的乳清蛋白水解剂 (MC5) 显示出作为高血压的饮食干预措施的巨大潜力.
- 这种结合计算方法和酶解水解的综合方法为开发功能性食品和营养药品提供了一种新的策略.
相关概念视频
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
382
The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
382
Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors
473
Angiotensin-converting enzyme (ACE), a vital component of the renin-angiotensin-aldosterone system, is abundant in lung endothelial cells. ACE converts the inactive decapeptide, angiotensin I, into the active octapeptide, angiotensin II. This potent vasoconstrictor narrows blood vessels, increasing resistance to blood flow and elevating blood pressure. Angiotensin II also stimulates aldosterone production, encouraging kidney cells to reabsorb more sodium and water from urine, thereby increasing...
473
Antihypertensive Drugs: Direct Renin Inhibitors
487
The renin-angiotensin-aldosterone system (RAAS) is an intricate physiological pathway involving numerous enzymes and hormones, including renin, angiotensin-converting enzyme (ACE), angiotensin I and II, and aldosterone. Imbalances within this system increase the production of angiotensin II and aldosterone. Increased angiotensin II levels promote vasoconstriction and blood pressure elevation. Concurrently, higher aldosterone levels stimulate sodium and water reabsorption in the kidneys,...
487
Antihypertensive Drugs: Action of Diuretics
617
Diuretics are antihypertensive drugs used to treat hypertension resulting from sodium and water retention. Sodium, vital for fluid balance and nerve or muscle function, is regulated by the kidneys through millions of nephrons. Blood enters nephrons via afferent arterioles, which branch into capillaries called glomeruli. These filter blood plasma, allowing water and solutes, like sodium ions, to pass through capillary walls into Bowman's capsule. The filtrate then flows through various...
617
Heart Failure Drugs: Diuretics
339
Heart failure and kidney perfusion are interconnected in a complex way. Reduced renal perfusion and venous congestion are two significant factors that contribute to renal dysfunction in heart failure. The kidneys, primarily responsible for fluid balance in the body, are adversely affected due to compromised cardiac output and increased venous pressure. In response to reduced renal perfusion, the kidneys activate neurohumoral mechanisms to restore balance. However, these mechanisms can be...
339
Antihypertensive Drugs: Potassium-Sparing Diuretics
448
Liddle syndrome is a genetically inherited form of hypertension characterized by the overactivity of epithelial sodium channels in the nephron, the functional unit of the kidney. This heightened activity leads to increased sodium reabsorption and excessive excretion of potassium. To counteract this, potassium-sparing diuretics such as amiloride are used. They function by blocking these sodium channels, thereby reducing the influx of sodium into the epithelial cells and minimizing the loss of...
448

