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Oxidative stress, antioxidants and intestinal calcium absorption

World Journal of Gastroenterology 2017年第16期23卷 2841-2853页

作者： gabriela diaz de barboza Solange Guizzardi Luciana Moine Nori Tolosa de Talamoni Laboratorio“Dr.Fernando Canas” Cátedra de Bioquímica y Biología MolecularFacultad de Ciencias MédicasINICSA(CONICET-Universidad Nacional de Córdoba)Pabellón ArgentinaCiudad UniversitariaCórdoba 5000Argentina

The disequilibrium between the production of reactive oxygen(ROS) and nitrogen(RNS) species and their elimination by protective mechanisms leads to oxidative stress. Mitochondria are the main source of ROS as by-products of electron transport chain. Most of the time the intestine responds adequately against the oxidative stress, but with aging or under conditions that exacerbate the ROS and/or RNS production, the defenses are not enough and contribute to developing intestinal pathologies. The endogenous antioxidant defense system in gut includes glutathione(GSH) and GSH-dependent enzymes as major components. When the ROS and/or RNS production is exacerbated, oxidative stress occurs and the intestinal Ca2+ absorption is inhibited. GSH depleting drugs such as DLbuthionine-S,R-sulfoximine, menadione and sodium deoxycholate inhibit the Ca2+ transport from lumen to blood by alteration in the protein expression and/or activity of molecules involved in the Ca2+ transcellular and paracellular pathways through mechanisms of oxidative stress, apoptosis and/or autophagy. Quercetin, melatonin, lithocholic and ursodeoxycholic acids block the effect of those drugs in experimental animals by their antioxidant, anti-apoptotic and/or anti-autophagic properties. Therefore, they may become drugs of choice for treatment of deteriorated intestinal Ca2+ absorption under oxidant conditions such as aging, diabetes, gut inflammation and other intestinal disorders.

关键词： Transcellular and paracellular Ca2+pathways DL-buthionine-S R-sulfoximine Menadione Sodium deoxycholate Lithocholic acid Ursodeoxycholic acid Melatonin

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Molecular aspects of intestinal calcium absorption

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World Journal of Gastroenterology 2015年第23期21卷 7142-7154页

作者： gabriela diaz de barboza Solange Guizzardi Nori Tolosa de Talamoni Cátedra de Bioquímica y Biología Molecular Facultad de Ciencias Médicas Universidad Nacional de Córdoba

Intestinal Ca2+ absorption is a crucial physiological process for maintaining bone mineralization and Ca2+ homeostasis. It occurs through the transcellular and paracellular pathways. The first route comprises 3steps: the entrance of Ca2+ across the brush border membranes(BBM) of enterocytes through epithelial Ca2+ channels TRPV6, TRPV5, and Cav1.3; Ca2+ movement from the BBM to the basolateral membranes by binding proteins with high Ca2+ affinity(such as CB9k); and Ca2+ extrusion into the blood. Plasma membrane Ca2+ ATPase(PMCA1b) and sodium calcium exchanger(NCX1) are mainly involved in the exit of Ca2+ from enterocytes. A novel molecule, the 4.1R protein, seems to be a partner of PMCA1 b, since both molecules colocalize and interact. The paracellular pathway consists of Ca2+ transport through transmembrane proteins of tight junction structures, such as claudins 2, 12, and 15. There is evidence of crosstalk between the transcellular and paracellular pathways in intestinal Ca2+ transport. When intestinal oxidative stress is triggered, there is a decrease in the expression of several molecules of both pathways that inhibit intestinal Ca2+ absorption. Normalization of redox status in the intestine with drugs such as quercetin, ursodeoxycholic acid, or melatonin return intestinal Ca2+ transport to control values. Calcitriol [1,25(OH)2D3] is the major controlling hormone of intestinal Ca2+ transport. It increases the gene and protein expression of most of the molecules involved in both pathways. PTH, thyroid hormones, estrogens, p ro l a c t i n, g ro w t h h o r m o n e, a n d g l u c o c o r t i c o i d s apparently also regulate Ca2+ transport by direct action, indirect mechanism mediated by the increase of renal 1,25(OH)2D3 production, or both. Different physiological conditions, such as growth, pregnancy, lactation, and aging, adjust intestinal Ca2+ absorption according to Ca2+ demands. Better knowledge of the molecular details of intestinal Ca2+ absorption could l

关键词： Intestinal Ca2+ absorption Transcellularpathway Paracellular route 1,25(OH)2D3 PTH Prolactin Estrogen Lactation Pregnancy Aging

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Glutathione depleting drugs, antioxidants and intestinal calcium absorption

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World Journal of Gastroenterology 2018年第44期24卷 4979-4988页

作者： Luciana Moine María Rivoira gabriela Díaz de barboza Adriana Pérez Nori Tolosa de Talamoni Laboratorio "Dr. Fernando Canas" Cátedra de Bioquímica y Biología Molecular Facultad de Ciencias Médicas INICSA (CONICET-Universidad Nacional de Córdoba) Córdoba 5000 Argentina

Glutathione （GSH） is a tripeptide that constitutes one of the main intracellular reducing compounds. The normal content of GSH in the intestine is essential to optimize the intestinal Ca2＋ absorption. The use of GSH depleting drugs such as DL-buthionine-S,R-sulfoximine, menadione or vitamin K3, sodium deoxycholate or diets enriched in fructose, which induce several features of the metabolic syndrome, produce inhibition of the intestinal Ca2＋ ab-sorption. The GSH depleting drugs switch the redox state towards an oxidant condition provoking oxida-tive/nitrosative stress and inflammation, which lead to apoptosis and/or autophagy of the enterocytes. Either the transcellular Ca transport or the paracellular Ca route are altered by GSH depleting drugs. The gene and/or protein expression of transporters involved in the transcellular Ca2＋ pathway are decreased. The favonoids quercetin and naringin highly abrogate the inhibition of intestinal Ca2＋ absorption, not only by restoration of the GSH levels in the intestine but also by their anti-apoptotic properties. Ursodeoxycholic acid, melatonin and glutamine also block the inhibition of Ca2＋ transport caused by GSH depleting drugs. The use of any of these antioxidants to ameliorate the intestinal Ca2＋ absorption under oxidant conditions associated with different pathologies in humans requires more investigation with regards to the safety,pharmacokinetics and pharmacodynamics of them.

关键词： Glutathione Transcellular and paracellular Ca^2+pathways DL-buthionine-S,R-sulfoximine Fructose rich diet Menadione Sodium deoxycholate Glutamine Ursodeoxycholic acid Melatonin Quercetin Naringin

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Nitrification inhibitor nitrapyrin does not affect yield-scaled nitrous oxide emissions in a tropical grassland

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Pedosphere 2021年第2期31卷 265-278页

作者： Ana gabriela PÉREZ-CASTILLO Cristina CHINCHILLA-SOTO Jorge Alberto ELIZONDO-SALAZAR Ronny barboza Dong-Gill KIM Christoph MÜLLER Alberto SANZ-COBENA Azam BORZOUEI Khadim DAWAR Mohammad ZAMAN Environmental Pollution Research Center(CICA) University of Costa RicaMontes de Oca 11501(Costa Rica) Alfredo Volio Mata Experimental Station University of Costa RicaOchomogo 30304(Costa Rica) Wondo Genet College of Forestry and Natural Resources Hawassa UniversityP.O.Box 128Shashemene(Ethiopia) Institute of Plant Ecology Justus Liebig University GiessenHeinrich-Buff Ring 26Giessen 35392(Germany) School of Biology and Environmental Science University College DublinBelfieldDublin 4(Ireland) Research Center for the Management of Environmental and Agricultural Risks(CEIGRAM) Department of Chemistry and Food Technology(ETSIAAB)Universidad Politécnica de MadridMadrid 28040(Spain) Nuclear Agriculture Research School Nuclear Science and Technology Research Institute(NSTRI)Karaj 31465-1498(Iran) department of Soil and Environmental Sciences The University of AgriculturePeshawar 25000(Pakistan) Soil and Water Management&Crop Nutrition Section Joint Food and Agriculture Organization(FAO)/International Atomic Energy Agency(IAEA)Division of Nuclear Techniques in Food and AgricultureDepartment of Nuclear Sciences and ApplicationsIAEAVienna International CentreP.O.Box 100Vienna 1400(Austria)

Urea is the most common nitrogen(N)fertilizer used in the tropics but it has the risk of high gaseous nitrogen(N)*** of nitrification inhibitor has been suggested as a potential mitigation measure for gaseous N losses in N fertilizer-applied *** a field trial on a tropical Andosol pastureland in Costa Rica,gaseous emissions of ammonia(NH_(3))and nitrous oxide(N_(2)O)and grass yield were quantified from plots treated with urea(U;41.7 kg N ha^(-1)application^(-1))and urea plus the nitrification inhibitor nitrapyrin(U+NI;41.7 kg N ha^(-1)application^(-1)and 350 g of nitrapyrin for each 100 kg of N applied)and control plots(without U and NI)over a six-month period(rainy season).Volatilization of NH_(3)(August to November)in U(7.4%±1.3%of N applied)and U+NI(8.1%±0.9%of N applied)were not significantly different(P>0.05).Emissions of N_(2)O in U and U+NI from June to November were significantly different(Pde protein production of grass were significantly higher(Pder typical N fertilizer application practices of pasturelands at the study site.

关键词： ammonia volatilization Andosol Costa Rica field trial gaseous N loss greenhouse gas emission urea

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