scholarly journals Contribution of Cholesterol and Oxysterols in the Physiopathology of Cataract: Implication for the Development of Pharmacological Treatments

2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
Anne Vejux ◽  
Mohammad Samadi ◽  
Gérard Lizard

The development of cataract is associated with some lipid changes in human lens fibers, especially with increased accumulation and redistribution of cholesterol inside these cells. Some direct and indirect lines of evidence, also suggest an involvement of cholesterol oxide derivatives (also named oxysterols) in the development of cataract. Oxysterol formation can result either from nonenzymatic or enzymatic processes, and some oxysterols can induce a wide range of cytotoxic effects (overproduction of reactive oxygen species (ROS); phospholipidosis) which might contribute to the initiation and progression of cataract. Thus, the conception of molecules capable of regulating cholesterol homeostasia and oxysterol levels in human lens fibers can have some interests and constitute an alternative to surgery at least at early stages of the disease.

2008 ◽  
Vol 177 (2) ◽  
pp. 97-107 ◽  
Author(s):  
Jyh-Ming Chow ◽  
Guan-Cheng Huang ◽  
Hui-Yi Lin ◽  
Shing-Chuan Shen ◽  
Liang-Yo Yang ◽  
...  

2006 ◽  
Vol 738 (1) ◽  
pp. 265-278 ◽  
Author(s):  
DAVID A. WINK ◽  
INGEBORG HANBAUER ◽  
FRANÇOISE LAVAL ◽  
JOHN A. COOK ◽  
MURALI C. KRISHNA ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-15 ◽  
Author(s):  
Manli Yang ◽  
Hassan Ahmed ◽  
Weidong Wu ◽  
Bijie Jiang ◽  
Zhenquan Jia

Atmospheric pollution has been a principal topic recently in the scientific and political community due to its role and impact on human and ecological health. 9,10-phenanthrenequinone (9,10-PQ) is a quinone molecule found in air pollution abundantly in the diesel exhaust particles (DEP). This compound has studied extensively and has been shown to develop cytotoxic effects both in vitro and in vivo. 9, 10-PQ has been proposed to play a critical role in the development of cytotoxicity via generation of reactive oxygen species (ROS) through redox cycling. This compound also reduces expression of glutathione (GSH), which is critical in Phase II detoxification reactions. Understanding the underlying cellular mechanisms involved in cytotoxicity can allow for the development of therapeutics designed to target specific molecules significantly involved in the 9,10-PQ-induced ROS toxicity. This review highlights the developments in the understanding of the cytotoxic effects of 9, 10-PQ with special emphasis on the possible mechanisms involved.


2020 ◽  
Vol 25 (2) ◽  
pp. 95
Author(s):  
Ameerah Tharek ◽  
Shaza Eva Mohamad ◽  
Koji Iwamoto ◽  
Iwane Suzuki ◽  
Hirofumi Hara ◽  
...  

Microalgae are known to be a potential resource of high-value metabolites that can be used in the growing field of biotechnology. These metabolites constitute valuable compounds with a wide range of applications that strongly enhance a bio-based economy. Among these metabolites, astaxanthin is considered the most important secondary metabolite, having superior antioxidant properties. For commercial feasibility, microalgae with enhanced astaxanthin production need to be developed. In this study, the tropical green microalgae strain, Coelastrum sp., isolated from the environment in Malaysia, was incubated with methyl viologen, a reactive oxygen species (ROS) reagent that generates superoxide anion radicals (O2-) as an enhancer to improve the accumulation of astaxanthin. The effect of different concentrations of methyl viologen on astaxanthin accumulation was investigated. The results suggested that the supplementation of methyl viologen at low concentration (0.001 mM) was successfully used as a ROS reagent in facilitating and thereby increasing the production of astaxanthin in Coelastrum sp. at a rate 1.3 times higher than in the control.


2009 ◽  
Vol 276 (1663) ◽  
pp. 1737-1745 ◽  
Author(s):  
Damian K. Dowling ◽  
Leigh W. Simmons

Evolutionary theory is firmly grounded on the existence of trade-offs between life-history traits, and recent interest has centred on the physiological mechanisms underlying such trade-offs. Several branches of evolutionary biology, particularly those focusing on ageing, immunological and sexual selection theory, have implicated reactive oxygen species (ROS) as profound evolutionary players. ROS are a highly reactive group of oxygen-containing molecules, generated as common by-products of vital oxidative enzyme complexes. Both animals and plants appear to intentionally harness ROS for use as molecular messengers to fulfil a wide range of essential biological processes. However, at high levels, ROS are known to exert very damaging effects through oxidative stress. For these reasons, ROS have been suggested to be important mediators of the cost of reproduction, and of trade-offs between metabolic rate and lifespan, and between immunity, sexual ornamentation and sperm quality. In this review, we integrate the above suggestions into one life-history framework, and review the evidence in support of the contention that ROS production will constitute a primary and universal constraint in life-history evolution.


2019 ◽  
Vol 6 (1) ◽  
pp. 43-47
Author(s):  
Azab Elsayed Azab ◽  
 Almokhtar A Adwas ◽  
Ata Sedik Ibrahim Elsayed ◽  
Almokhtar A Adwas ◽  
 Ata Sedik Ibrahim Elsayed ◽  
...  

The present review aims to high light on the oxidative stress, and prevention by internal antioxidants and external antioxidants by some natural products possessing antioxidant properties. Oxidative stress occurs when the balance between reactive oxygen species (ROS) formation and detoxification favors an increase in ROS levels, leading to disturbed cellular function. ROS causes damage to cellular macromolecules causing lipid peroxidation, nucleic acid, and protein alterations. Their formation is considered as a pathobiochemical mechanism involved in the initiation or progression phase of various diseases such as atherosclerosis, ischemic heart diseases, diabetes, and initiation of carcinogenesis or liver diseases. In order to maintain proper cell signaling, it is likely that a number of radical scavenging enzymes maintain a threshold level of ROS inside the cell. However, when the level of ROS exceeds this threshold, an increase in ROS production may lead to excessive signals to the cell, in addition to direct damage to key components in signaling pathways. ROS can also irreversibly damage essential macromolecules. Protein-bound thiol and non-protein-thiol are the major cytosolic low molecular weight sulfhydryl compound that acts as a cellular reducing and a protective reagent against numerous toxic substances including most inorganic pollutants, through the –SH group. Hence, thiol is often the first line of defense against oxidative stress. Flavonoids have been found to play important roles in the non-enzymatic protection against oxidative stress, especially in the case of cancer. Flavonoids have occurred widely in tea, fruit, red wine, vegetables, and cocoas. Flavonoids, including flavones, flavanone, flavonols, and isoflavones, are polyphenolic compounds which are widespread in foods and beverages, and possess a wide range of biological activities, of which anti-oxidation has been extensively explored. It can be concluded that oxidative stress causes irreversible damage in cellular macromolecules that leads to initiation of various diseases such as atherosclerosis, ischemic heart diseases, liver diseases, diabetes, and initiation of carcinogenesis. Antioxidants inhibit reactive oxygen species production and scavenging of free radicals. Therefore, the review recommends that high consumption of natural foods that are rich in antioxidants will provide more protection against toxic agents and related diseases.


Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 4300-4300
Author(s):  
Serge Côté ◽  
Nathalie Dussault ◽  
Carl Simard

Abstract Hematopoietic cells mature in the bone marrow under the control of a diversity of growth factors and the influence of various cell types producing superoxide and other reactive oxygen species (ROS). As ROS may regulate activities of redox-sensitive enzymes implicated in a wide range of cellular processes, we have exposed the human megakaryocytic cell line M-07e to hydrogen peroxide (H2O2) at concentrations that increased intracellular ROS and examined whether expression of the megakaryocytic programme could be enhanced. The growth-factor dependent M-07e cells display surface markers characteristic of both early myeloid progenitors and more committed members of the magakaryocyte (Mk) lineage, such as glycoproteins GPIIb-IIIa (CD41) and GPIb (CD42). H2O2 significantly reduced cell proliferation without affecting viability. After 4 days of exposure to this reagent, expression of the early Mk marker CD41 was 1.2 times higher than that of control cells. Although no change in the expression of the late Mk marker CD42 was detected, exposure to H2O2 was found to increase the incidence of multinucleate cells, polyploidy and abnormal microtubule organising centre numbers. Investigation of this phenomenon on synchronized M-07e cells revealed that H2O2 arrested cytokinesis at a late stage and that some nuclei were still able to incorporate bromodeoxyuridine (BrdU). Cell division was similarly impaired when M-07e cells were either exposed to botulin toxin C3 transferase or Y-27362 inhibitor, suggesting that H2O2 treatments affected members of the Rho family of small GTP-binding proteins and/or their effectors. Together, these findings indicate that endoreplication in Mk may be linked to changes in the cellular redox state of these cells and support the concept that differentiation and polyploidization are independently regulated events.


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