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Oxidative stress nitric oxide

Freese R, Basu S, Hietanen E, Nair J, Nakachi K, Bartsch H, Mutanen M. 1999. Green tea extract decreases plasma malondialdehyde concentration but does not affect other indicators of oxidative stress, nitric oxide production, or hemostatic factors during a high-linoleic acid diet in healthy females. Eur J Nutr 38 149-157. [Pg.152]

Li, H., Horke, S., Forstermann, U., 2014. Vascular oxidative stress, nitric oxide and atherosclerosis. Atherosclerosis 237, 208—219. [Pg.200]

Kudo FA, Warycha B, Juran PJ, Asada H, Teso D, Aziz F (2005) Differential responsiveness of early- and late-passage endothehal cells to shear stress. Am J Surg 190(5) 763-769 Lee RH, Efron D, Tantry U, Barbul A (2001) Nitric oxide in the healing wound a time-course study. J Surg Res 101(1) 104-108... [Pg.349]

The vascular endothelium produces a number of substances that are released basally into the blood vessel wall to alter vascular smooth muscle tone. One such substance is endothelin (ET-1). Endothelin exerts its effects throughout the body, causing vasoconstriction as well as positive inotropic and chronotropic effects on the heart. The resulting increases in TPR and CO contribute to an increase in MAP. Synthesis of endothelin appears to be enhanced by many stimuli, including Ag II, vasopressin, and the mechanical stress of blood flow on the endothelium. Synthesis is inhibited by vasodilator substances such as prostacyclin, nitric oxide, and atrial natriuretic peptide. There is evidence that endothelin is involved with the pathophysiology of many cardiovascular diseases, including hypertension, heart failure, and myocardial infarction. Endothelin receptor antagonists are currently available for research use only. [Pg.210]

D.L. Kellogg, J.L. Zhao, C. Friel and LJ. Roman, Nitric oxide concentration increases in the cutaneous interstitial space during heat stress in humans. J. Appl. Physiol. 94, 1971-1977 (2003). [Pg.52]

In conclusion, it should be stressed that the competition between pro- and antiapoptotic effects of nitric oxide must probably depends on its relevant levels [137] the low physiological levels of NO principally suppress the apoptotic pathway by several mechanisms, whereas the higher rates of NO production may overcome cellar protective mechanisms and stimulate apoptosis. Furthermore, the simultaneous formation of nitric oxide and superoxide increases the possibility of apoptosis activation due to the formation of peroxynitrite. [Pg.759]

Belkner et al. [32] demonstrated that 15-LOX oxidized preferably LDL cholesterol esters. Even in the presence of free linoleic acid, cholesteryl linoleate continued to be a major LOX substrate. It was also found that the depletion of LDL from a-tocopherol has not prevented the LDL oxidation. This is of a special interest in connection with the role of a-tocopherol in LDL oxidation. As the majority of cholesteryl esters is normally buried in the core of a lipoprotein particle and cannot be directly oxidized by LOX, it has been suggested that LDL oxidation might be initiated by a-tocopheryl radical formed during the oxidation of a-tocopherol [33,34]. Correspondingly, it was concluded that the oxidation of LDL by soybean and recombinant human 15-LOXs may occur by two pathways (a) LDL-free fatty acids are oxidized enzymatically with the formation of a-tocopheryl radical, and (b) the a-tocopheryl-mediated oxidation of cholesteryl esters occurs via a nonenzymatic way. Pro and con proofs related to the prooxidant role of a-tocopherol were considered in Chapter 25 in connection with the study of nonenzymatic lipid oxidation and in Chapter 29 dedicated to antioxidants. It should be stressed that comparison of the possible effects of a-tocopherol and nitric oxide on LDL oxidation does not support importance of a-tocopherol prooxidant activity. It should be mentioned that the above data describing the activity of cholesteryl esters in LDL oxidation are in contradiction with some earlier results. Thus in 1988, Sparrow et al. [35] suggested that the 15-LOX-catalyzed oxidation of LDL is accelerated in the presence of phospholipase A2, i.e., the hydrolysis of cholesterol esters is an important step in LDL oxidation. [Pg.810]

Wassmann S, Laufs U, Stamenkovic D, Linz W, Stasch JP, Ahlbory K, Rosen R, Bohm M, Nickening G (2002) Raloxifene improves endothelial dysfunction in hypertension by reduced oxidative stress and enhanced nitric oxide production. Circulation 105 2083-2091... [Pg.90]

Intramuscular injection of turpentine causes a biphasic HPA response [33], The first phase corresponds to the stress of injection with no detectable changes in plasma IL-6 concentrations. However, the second phase coincides with an inflammatory response to the turpentine, a response accompanied by increased plasma ACTH, corticosterone, and IL-6 levels. CRH, AVP, and PGs play stimulatory roles in this model, whereas nitric oxide dampens the pituitary response [33], IL-ip may be important for triggering the release of these signaling molecules, since mice lacking the gene for IL-ip have a blunted GC response to turpentine [34],... [Pg.496]

Redox reactions involving nitric oxide have important implications beyond their fundamental chemistry as demonstrated by the controversy in the biomedical literature regarding conditions under which generation of NO leads to the amelioration or the exacerbation of oxidative stress in mammalian systems (95). Oxidative stress is defined as a disturbance in the balance between production of reactive oxygen species (pro-oxidants) and antioxidant defenses (96). Reactive oxygen species include free radicals and peroxides as well as other reactants such as oxidative enzymes with metal ion sites in high oxidation states. The... [Pg.233]

Vardi A, Formiggini F, Casotti R, De Martino A, Ribalet F, Miralto A, Bowler C (2006) A stress surveillance system based on calcium and nitric oxide in marine diatoms. PLoS Biol 4 411 119 Vorwerk S, Somerville S, Somerville C (2004) The role of plant cell wall polysaccharide composition in disease resistance. Trends Plant Sci 9 203-209 Vreeland V, Laetsch WM (1990) A gelling carbohydrate in algal cell wall formation. In Adair WS, Mecham RP (eds) Organization and assembly of plant and animal extracellular matrix. Academic, San Diego, CA, ppl 37—171... [Pg.270]


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See also in sourсe #XX -- [ Pg.141 ]




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