Whole milk protein powder separated by low-temperature nanofiltration membrane administration alleviates sepsis-induced myopathy

• Published in: Nutrition & metabolism Vol. 21; no. 1; pp. 85 - 16
• Main Authors: Li, Na, Lan, Junyu, Yang, Jianjun, Ding, Huan
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 25.10.2024; BioMed Central; BMC
• Subjects: AMPK/mTOR signal pathway; Analysis; Care and treatment; Collagen; Complications and side effects; Health aspects; Medical examination; Milk proteins; Mitochondria function; Muscles; Physiology, Pathological; Sepsis; Sepsis-induced myopathy; Whole milk protein powder; China; Whole milk protein powder; Mitochondria function; AMPK/mTOR signal pathway; Sepsis-induced myopathy
• ISSN: 1743-7075; 1743-7075
• DOI: 10.1186/s12986-024-00862-4

Sepsis-induced myopathy (SIM) has been recognized as a critical risk factor for the development of acquired muscle weakness among patients in the intensive care unit. These individuals frequently encounter inadequate dietary intake and malnutrition. With the aggravation of the severity of the person's condition, leading to increased skeletal muscle protein breakdown and reduced synthesis, which is an urgent problem to be solved in clinical nutritional treatment. Whole milk protein powder (WMPP) has promising bioactive nutrients and holds promising potential for enhancing skeletal muscle mass. The study was designed to delve into the potential effects and mechanisms of WMPP intervention for increaseing skeletal muscle mass on SIM mice. Our results clearly show that the intervention with WMPP can significantly improve the exercise capacity and skeletal muscle mass in SIM mice. It significantly increases the diameter and cross-sectional area (CSA) of skeletal muscle fibers, while effectively reducing the excessive aggregation of collagen fibers and the abnormal accumulation of adipose tissue in the skeletal muscle of SIM mice. Moreover, WMPP intervention also significantly alleviated the oxidative stress status of mitochondria, which subsequently enhanced the expression of mitochondrial metabolic enzymes. The mechanism may be associated with decreased AMPK phosphorylation in skeletal muscle tissue and simultaneously increased phosphorylation of mTOR, p70S6K1, and 4EBP-1 in SIM mice. In summary, the WMPP intervention significantly enhances exercise capacity and skeletal muscle mass while mitigating the oxidative stress status of mitochondria. Furthermore, it regulates skeletal muscle anabolism via the AMPK/mTOR signaling pathway in SIM mice.