The metabolic response to stress: an overview and update

Abstract

Recent investigation has demonstrated that the response to stress is mediated by complex interactions between the nervous, endocrine, immune, and hematopoietic systems. Not only is the neuroendocrine system operative but monokines and lymphokines, such as IL-1, IL-6, and TNF, also play important roles. The discovery of these mediators, along with that of macrophage-derived substances that operate at the local wound level, such as platelet-derived, basic fibroblast, transforming, and epidermal growth factors, coupled with advances in molecular biology portends much for the future. The ability to alter the endocrine response with techniques such as epidural anesthesia, the ability to specifically block certain aspects of the response (e.g., with adrenergic and prostaglandin antagonists), and the ability to synthesize potential beneficial mediators with recombinant DNA techniques (e.g., GH) may allow for modulating the response to decrease debility and complications.