Abstract

A dose-response relationship to stressors, according to the hormesis theory, is characterized by low-dose stimulation and high-dose inhibition. It is non-linear with a low-dose optimum. Stress responses by cells lead to adapted vitality and fitness. Physical stress can be exerted through heat, radiation, or physical exercise. Chemical stressors include reactive species from oxygen (ROS), nitrogen (RNS), and carbon (RCS), carcinogens, elements, such as lithium (Li) and silicon (Si), and metals, such as silver (Ag), cadmium (Cd), and lead (Pb). Anthropogenic chemicals are agrochemicals (phytotoxins, herbicides), industrial chemicals, and pharmaceuticals. Biochemical stress can be exerted through toxins, medical drugs (e.g., cytostatics, psychopharmaceuticals, non-steroidal inhibitors of inflammation), and through fasting (dietary restriction). Key-lock interactions between enzymes and substrates, antigens and antibodies, antigen-presenting cells, and cognate T cells are the basics of biology, biochemistry, and immunology. Their rules do not obey linear dose-response relationships. The review provides examples of biologic stressors: oncolytic viruses (e.g., immuno-virotherapy of cancer) and hormones (e.g., melatonin, stress hormones). Molecular mechanisms of cellular stress adaptation involve the protein quality control system (PQS) and homeostasis of proteasome, endoplasmic reticulum, and mitochondria. Important components are transcription factors (e.g., Nrf2), micro-RNAs, heat shock proteins, ionic calcium, and enzymes (e.g., glutathion redox enzymes, DNA methyltransferases, and DNA repair enzymes). Cellular growth control, intercellular communication, and resistance to stress from microbial infections involve growth factors, cytokines, chemokines, interferons, and their respective receptors. The effects of hormesis during evolution are multifarious: cell protection and survival, evolutionary flexibility, and epigenetic memory. According to the hormesis theory, this is true for the entire biosphere, e.g., archaia, bacteria, fungi, plants, and the animal kingdoms.

Highlights

  • Hormesis describes a dose-response relationship to stressors with a low-dose stimulation and high-dose inhibition

  • This review has reported the positive hormetic effects of transient dietary restriction (DR) and intermittent metabolic switching (IMS)

  • Hormesis is an important principle in the global biosphere with implications in many fields

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Summary

Introduction

Hormesis describes a dose-response relationship to stressors with a low-dose stimulation and high-dose inhibition. Hormesis is an evolutionary ancient biphasic dose-response of cells and it is a highly generalizable phenomenon [2]. A hormesis database from 2005 contains 5600 dose-response relationships over about 900 broadly diversified chemicals and physical agents [3]. The linear non-threshold model (LNTM) extrapolates the late effects of high-dose exposure to ionizing radiation to the low-dose range and it is the cornerstone of. Hormesis has emerged as a central concept of risk assessment for carcinogens and non-carcinogens. It has significant implications for clinical medicine [6]. Hormesis effects are described in plant cells with implications for agriculture. This review sheds light on the archaic origin of the adaptive stress response and elucidates its global validity

The Beginnings
Nrf2 and Its Role in Anti-Oxidative and Anti-Inflammatory Cellular Responses
Inhibition of nuclear translocation via Nrf2
LDR and Innate Immunity
LDR and Adaptive Immunity
Other Hormetic Effects in the Immune System
Protection by Immunological Memory
Hormetic Effects on the Immune System by Sportive Exercise
Low Stimulatory Effects of Toxic Compounds
Psychiatry
Neurodegenerative Diseases
Metabolic Syndrom
Autoimmune Diseases
Multidrug Interaction
Historic Aspects
Hormetic Aspects of Antigen Recognition by the Immune System
Low-Dose T Cell Triggering and Cytotoxic Effector Function
Peptide-Based Vaccines
Hormesis Effects in Plants
Archaic Environmental Stress Response as an Example of Hormesis
Global Aspects
Findings
10. Discussion
11. Summary and Conclusions
Full Text
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