scholarly journals Nutrition, hormetic stress and health

2005 ◽  
Vol 18 (2) ◽  
pp. 249-258 ◽  
Author(s):  
David G. Lindsay

Hormesis defines an effect where exposure to a low dose of a toxic agent results in a beneficial response. It has been described in organisms exposed to low-dose radiation, heat stress, and chemicals. The effect is characterised by a J-shaped dose–response as opposed to a linear dose–response. Confirmation of the general phenomena of hormesis has proved difficult due to the lack of appropriate methodology and the absence of well-defined mechanisms to support the experimental observations. In the nutritional field there are few reports of its existence. The clearest illustration of the effect is seen in animals that are energy restricted when there is a clear benefit in the reduction of age-related disease, and an extension of maximum lifespan. DNA microarray experiments have shown that there is a down regulation of the stress-response genes that are up regulated through the ageing process. Electrophilic phytochemicals, that have been shown to have beneficial health effects at low doses, up regulate the antioxidant–electrophile response element. This probably occurs through an alteration in the redox state of the target cells which causes activation of protein kinases, the activation of the Nrf2 transcription factor and the up regulation of the phase II enzymes, similar to responses that occur under mild chemical stress. This situation might enable organisms to adapt to stress such that the effects of a subsequent exposure to a harmful challenge are reduced. There may be a permanent alteration in cellular homeostasis, or redox state, if the low level exposure is maintained. It remains to be proven if such a situation occurs in response to chronic low-dose exposure to dietary phytochemicals such that the target cells are better able to respond to a subsequent stress challenge.

2013 ◽  
Vol 85 (4) ◽  
pp. 959-964 ◽  
Author(s):  
Eugene Chung ◽  
James R. Corbett ◽  
Jean M. Moran ◽  
Kent A. Griffith ◽  
Robin B. Marsh ◽  
...  

Author(s):  
Gusti Ngurah Sutapa ◽  
Ni Nyoman Ratini ◽  
Ni Kadek Nova Anggarani ◽  
I Gde Antha Kasmawan

One of the phenomena of the low-dose radiation effect is the radio adaptation response which is an important part of the response of molecules, cells, and body tissues to ionizing radiation. The phenomenon of radio adaptation response is a response that occurs when changes in gene expression can be induced by exposure to low doses of radiation (<0.5 Gy). Changes in the expression of this gene under certain circumstances serve to protect cells against the effects caused by subsequent exposure to higher doses of radiation, so this situation is known as an adaptive response or radio adaptation response. Cells can respond to very low doses of radiation with some changes in gene expression. Beginning with the administration of radiation to cells with a very low dose, known as the adaptation dose (AD), and then in a short period being given a larger dose of radiation, known as the challenge dose (CD), there was a decrease in the number of induced chromosome aberrations when compared to cells that were not irradiated at an adapted dose. The purpose of this study was to obtain a radiotherapy method that could show a reduction in the patient's dose.


2016 ◽  
Vol 31 (Suppl 1) ◽  
pp. S10 ◽  
Author(s):  
Ki Moon Seong ◽  
Songwon Seo ◽  
Dalnim Lee ◽  
Min-Jeong Kim ◽  
Seung-Sook Lee ◽  
...  

2020 ◽  
Vol 2020 (56) ◽  
pp. 97-113 ◽  
Author(s):  
Amy Berrington de Gonzalez ◽  
Robert D Daniels ◽  
Elisabeth Cardis ◽  
Harry M Cullings ◽  
Ethel Gilbert ◽  
...  

Abstract Whether low-dose ionizing radiation can cause cancer is a critical and long-debated question in radiation protection. Since the Biological Effects of Ionizing Radiation report by the National Academies in 2006, new publications from large, well-powered epidemiological studies of low doses have reported positive dose-response relationships. It has been suggested, however, that biases could explain these findings. We conducted a systematic review of epidemiological studies with mean doses less than 100 mGy published 2006–2017. We required individualized doses and dose-response estimates with confidence intervals. We identified 26 eligible studies (eight environmental, four medical, and 14 occupational), including 91 000 solid cancers and 13 000 leukemias. Mean doses ranged from 0.1 to 82 mGy. The excess relative risk at 100 mGy was positive for 16 of 22 solid cancer studies and 17 of 20 leukemia studies. The aim of this monograph was to systematically review the potential biases in these studies (including dose uncertainty, confounding, and outcome misclassification) and to assess whether the subset of minimally biased studies provides evidence for cancer risks from low-dose radiation. Here, we describe the framework for the systematic bias review and provide an overview of the eligible studies.


2003 ◽  
Vol 1 (1) ◽  
pp. 154014203908444 ◽  
Author(s):  
Shu-Zheng Liu

The health effects of low-dose radiation (LDR) have been the concern of the academic spheres, regulatory bodies, governments, and the public. Among these effects, the most important is carcinogenesis. In view of the importance of immune surveillance in cancer control, the dose-response relationship of the changes in different cell types of the immune system after whole-body irradiation is analyzed on the basis of systemic data from the author's laboratory in combination with recent reports in the literature. For T lymphocytes J- or inverted J-shaped curves are usually demonstrated after irradiation, while for macrophages dose-response curves of chiefly stimulation with irregular patterns are often observed. The intercellular reactions between the antigen presenting cell (APC) and T lymphocyte (TLC) in the immunologic synapse via expression of surface molecules and secretion of cytokines by the two cell types after different doses of radiation are illustrated. The different pathways of signal transduction thus facilitated in the T lymphocyte by different doses of radiation are analyzed to explain the mechanism of the phenomenon of low-dose stimulation and high-dose suppression of immunity. Experimental and clinical data are cited to show that LDR retards tumor growth, reduces metastasis, increases the efficacy of conventional radiotherapy and chemotherapy as well as alleviates the suppression of immunity due to tumor burden. The incidence of thymic lymphoma after high-dose radiation is lowered by preexposure to low-dose radiation, and its mechanism is supposed to be related to the stimulation of anticancer immunity induced by low-dose radiation. Recent reports on lowering of standardized cancer mortality rate and all cause death rate of cohorts occupationally exposed to low-dose radiation from the US, UK, and Canada are cited.


2003 ◽  
Vol 1 (1) ◽  
pp. 154014203908444 ◽  
Author(s):  
Bobby R. Scott ◽  
Dale M. Walker ◽  
Yohannes Tesfaigzi ◽  
Helmut Schöllnberger ◽  
Vernon Walker

The linear nonthreshold (LNT) model plays a central role in low-dose radiation risk assessment for humans. With the LNT model, any radiation exposure is assumed to increase one's risk of cancer. Based on the LNT model, others have predicted tens of thousands of deaths related to environmental exposure to radioactive material from nuclear accidents ( e.g., Chernobyl) and fallout from nuclear weapons testing. Here, we introduce a mechanism-based model for low-dose, radiation-induced, stochastic effects (genomic instability, apoptosis, mutations, neoplastic transformation) that leads to a LNT relationship between the risk for neoplastic transformation and dose only in special cases. It is shown that nonlinear dose-response relationships for risk of stochastic effects (problematic nonlethal mutations, neoplastic transformation) should be expected based on known biological mechanisms. Further, for low-dose, low-dose rate, low-LET radiation, large thresholds may exist for cancer induction. We summarize previously published data demonstrating large thresholds for cancer induction. We also provide evidence for low-dose-radiation-induced, protection (assumed via apoptosis) from neoplastic transformation. We speculate based on work of others ( Chung 2002 ) that such protection may also be induced to operate on existing cancer cells and may be amplified by apoptosis-inducing agents such as dietary isothiocyanates.


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