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Melatonin and the pathophysiology of

Year 2010, Volume: 14 Issue: 1, 1 - 9, 03.03.2014

Abstract

References

  • Tan DX, Chen LD, Poeggeler B, Manchester LC, Reiter RJ. Melatonin: a potent, endogenous hydroxyl radical scav- enger. Endocrine J, 1: 57-60, 1993.
  • Reiter RJ. Functional pleotrophy of the neurohormone melatonin: antioxidant protection and neuroendocrine regulation. Front Neuroendocrinol, 16: 383-415, 1995.
  • Reiter RJ, Tan DX, Kim SJ, Qi W. Melatonin as a pharma- cological agent against oxidative damage to lipids and DNA. Proc West Pharmacol Soc, 41: 229-236, 1998.
  • Manda K, Ueno M, Anzai K. AFMK, a melatonin metabo- lite, attenuates X-ray-induced oxidative damage to DNA, proteins and lipids in mice. J Pineal Res, 42: 386-393, 2007.
  • Maldonado MD, Murillo-Cabezas F, Terron MP, Flores LJ, Tan DX, Manchester LC, Reiter RJ.The potential of mela- tonin in reducing morbidity-mortality after craniocerebral trauma. J Pineal Res, 42: 1-11, 2007.
  • Tengattini, S, Reiter RJ, Tan DX, Terron MP, Rodella LF. Cardiovascular diseases: protective effects of melatonin. J Pineal Res, 44: 16-25, 2008.
  • Tan DX, Manchester LC, Reiter RJ, Plummer BF, Limson J, Weintraub ST, Qi W. Melatonin directly scavenges hy- drogen peroxide: a potentially new metabolic pathway of melatonin biotransformation. Free Radic Biol Med, 29: 1177-1185, 2000.
  • Tan DX, Manchester LC, Terron MP, Flores LJ, Reiter RJ. One molecule, many derivatives: a never ending interac- tion of melatonin with reactive oxygen and nitrogen spe- cies? J Pineal Res, 42: 28-42, 2007.
  • Pappolla MA, Chyan YJ, Poeggeler B, Frangione B, Wil- son G, Ghiso J, et al. An assessment of the antioxidant and antiamyloidogenic properties of melatonin: implications for Alzheimer’s disease. J Neural Transm, 107: 203-231, 2000.
  • Reiter RJ, Tan DX, Manchester LC, Qi W. Biochemical re- activity of melatonin with reactive oxygen and nitrogen species: a review of the evidence. Cell Biochem Biophys, 34: 237-256, 2001.
  • Reiter RJ, Tan DX, Manchester LC, El-Sawi MR. Melatonin reduces oxidative damage and promotes mitochondrial respiration: implications for aging. Ann NY Acad Sci, 959: 238-250, 2002.
  • Allegra M, Reiter RJ, Tan DX, Gentile C, Tesoriere L, Liv- rea MA. The chemistry of melatonin’s interaction with re- active species. J Pineal Res, 34:1-10, 2003.
  • Hardeland R. Antioxidative protection by melatonin: multiplicity of mechanisms from radical detoxification to radical avoidance. Endocrine, 27: 119-130, 2005.
  • Hardeland R, Backhaus C, Fadavi A. Reactions of the NO redox forms NO+, .NO and HNO (protonated NO-) with the melatonin metabolite N1-acetyl-5-methoxyky- puramine. J Pineal Res, 43: 382-388, 2007.
  • Zavodnik IB, Domanski AV, Lapshina EA, Bryszewska M, Reiter RJ. Melatonin directly scavenges peroxyl and alkoxyl radicals generated in red blood cells and a cell- free system: chemiluminescence measurements and theo- retical calculations. Life Sci, 79: 391-400, 2006.
  • Peyrot N, Ducrocq C. Potential role of tryptophan deriva- tives in stress responses characterized by the generation of reactive oxygen and nitrogen species. J Pineal Res, 45: 235-246. 2008.
  • Tan DX, Reiter RJ, Manchester LC, Yan MT, El-Sawi M, Sainz RM, Mayo JC, Kohen R, Allegra M, Hardeland R. Chemical and physical properties and potential mecha- nisms: melatonin as a broad spectrum antioxidant and free radical scavenger. Curr Topics Med Chem, 2: 181- 198, 2002.
  • Tan DX, Manchester LC, Sainz RM, Mayo JC, Alvarez F, Reiter RJ. Antioxidant strategies in protection against neurodegenerative disorders. Expert Opin Ther Patents, 13: 1513-1542, 2003.
  • Pablos MI, Agapito MT, Gutierrez R, Recio JM, Reiter RJ, Barlow-Walden L, Acuña-Castroviejo D, Menendez- Pelaez A. Melatonin stimulates the activity of the detoxi- fying enzyme glutathione peroxidase in several tissues of chicks. J Pineal Res, 19: 111-115, 1995.
  • Reiter RJ, Tan DX, Osuna C, Gitto E. Actions of melaton- in in the reduction of oxidative stress: a review. J Biomed Res, 7: 444-458, 2000.
  • Rodriguez C, Mayo JC, Sainz RM, Antolín I, Herrera F, Martín V, Reiter RJ. Regulation of antioxidant enzymes: a significant role for melatonin. J Pineal Res, 36: 1-9, 2004.
  • Tomas-Zapico C, Coto-Montes A. A proposed mecha- nism to explain the stimulatory effect of melatonin on antioxidative enzymes. J Pineal Res, 39: 99-104, 2005.
  • Leon J, Escames G, Rodriguez MI, López LC, Tapias V, Entrena A, Camacho E, Carrión MD, Gallo MA, Espinosa A, Tan DX, Reiter RJ, Acuña-Castroviejo D. Inhibition of neuronal nitric oxide synthase activity by N1-acetyl- 5methoxykynuramine, a brain metabolite of melatonin. J Neurochem, 98: 2023-2033, 2006.
  • Urata Y, Honma S, Goto S, Todoroki S, Iida T, Cho S, Hon- ma K, Kondo T. Melatonin induces gamma-glutamyl- cysteine synthase mediated by activator protein-1 in hu- man vascular endothelial cells. Free Radic Biol Med, 27: 838-847, 1999.
  • Winiarska K, Fraczyk T, Molinska D, Drozak J, Bryla J. Melatonin attenuates diabetes-induced oxidative stress in rabbits. J Pineal Res, 40: 168-176, 2006.
  • Sainz RM, Reiter RJ, Tan DX, Roldan F, Natarajan M, Quiros I, Hevia D, Rodriguez C, Mayo JC. Critical role of glutathione in melatonin enhancement of tumor necrosis factor and ionizing radiation-induced apoptosis in pros- tate cancer cells in vitro. J Pineal Res, 45: 258-270, 2008.
  • Okatani Y, Wakasuki A, Reiter RJ. Hepatic mitochondri- al dysfunction in senescence-accelerated mice: correction by long-term, orally administered physiological levels of melatonin. J Pineal Res, 33: 127-133, 2002.
  • Martin M, Macias M, Escames G, Reiter RJ, Agapito MT, Ortiz GG, Acuña-Castroviejo D. Melatonin-induced in- creased activity of the respiratory complexes I and IV can prevent mitochondrial damage induced by ruthe- nium red in vivo. J Pineal Res, 28: 242-248, 2000.
  • Leon J, Acuna-Castroviejo D, Escames G, Tan DX, Re- iter RJ. Melatonin mitigates mitochondrial malfunction. J Pineal Res, 38: 1-9, 2005.
  • Reiter RJ, Paredes SD, Korkmaz A, Jou MJ, Tan DX. Me- latonin combats molecular terrorism at the mitochondri- al level. Interdisc Toxicol, 1: 137-149, 2008.
  • Jou MJ, Peng TI, Yu PZ, Jou SB, Reiter RJ, Chen JY, Wu HY, Chen CC, Hsu LF. Melatonin protects against com- mon deletion of mitochondria DNA-augmented mito- chondrial oxidative stress and apoptosis. J Pineal Res, 43: 389-403, 2007.
  • Jou, MJ, Peng TI, Reiter RJ, Jou SB, Wu HY, Wen ST. Visualization of the antioxidative effects of melatonin at the mitochondrial level during oxidative stress-induced apoptosis of rat brain astrocytes. J Pineal Res, 37: 55-70, 2004.
  • Cervantes M, Morali G, Letechipia-Vallejo G. Melatonin and ischemia-reperfusion injury. J Pineal Res, 45: 1-7, 2008.
  • De Filippis D, Iuvone T, Esposito G, Steardo L, Arnold GH, Paul AP, De Man Joris G, De Winter Benedicte Y. Melatonin reverses lipopolysaccharide-induced gastro- intestinal mobility disturbances through the inhibition of oxidative stress. J Pineal Res, 44: 45-51, 2008.
  • Tamura H, Takasaki A, Miwa I, Taniguchi K, Maekawa R, Asada H, Taketani T, Matsuoka A, Yamagata Y, Shi- mamura K, Morioka H, Ishikawa H, Reiter RJ, Sugino N. Oxidative stress impairs oocyte quality and melatonin protects oocytes from free radical damage and improves fertilization rate. J Pineal Res, 44: 280-287, 2008.
  • Gitto E, Pelligrino S, Gitto P, Barberi I, Reiter RJ. Oxida- tive stress of the newborn in the pre-and post-natal pe- riod and the clinical utility of melatonin. J Pineal Res, 46: 128-139, 2009.
  • Gitto E, Karbownik M, Reiter RJ, Tan DX, Cuzzocrea S, Chiurazzi P, Cordaro S, Corona G, Trimarchi G, Barberi I. Effects of melatonin treatment in septic newborns. Pediatr Res, 50: 756-760, 2000.
  • Fulia F, Gitto E, Cuzzocrea S, Reiter RJ, Dugo L, Gitto P, Barberi S, Cordaro S, Barberi I. Increased levels of malondialdehyde and nitrite/nitrate in the blood of as- phyxiated newborns: reduction by melatonin. J Pineal Res, 31: 343-349, 2001.
  • Kucukakin B, Lykkesfeldt J, Nielsen HJ, Reiter RJ, Rosen- berg J, Gogenur I. Utility of melatonin to treat surgical stress after major vascular surgery – a safety study. J Pin- eal Res, 44: 426-431, 2008.
  • Melchiorri D, Reiter RJ, Sewerynek E, Chen LD, Nistico G. Melatonin reduces kainate-induced lipid peroxida- tion in homogenates of different brain regions. FASEB J, 9:1205-1210, 1995.
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Melatonin and the pathophysiology of cellular membranes

Year 2010, Volume: 14 Issue: 1, 1 - 9, 03.03.2014

Abstract

ABSTRACT: The ability of melatonin to influence the physiology of cell membranes is reviewed
in this report. Publications related to this field from 1993 – present. Melatonin is a
ubiquitously acting indoleamine which is associated with a variety of important functions
within both unicellular and multicellular organisms. By virtue of its ability to protect lipids
from free radical damage, melatonin is remarkably beneficial in preserving the morphological
and functional integrity of cell membranes. In doing so, it reduces the quantity of oxidized
lipids in membranes and maintains them at optimal fluidity, i.e., prevents them from
becoming rigid. This contributes significantly to the function of proteins (receptors, channels,
pores, etc.) in the cell membranes and helps in preserving the normal physiology of the
cells. In addition to these indirect effects of melatonin on membrane function, there is evidence
that this indoleamine also may act directly on channels assisting membranes in maintaining
proper ion gradients and current. The role of melatonin in the functioning of membrane
channels and pores is an area of research that should be experimentally exploited.
KEY WORDS: Melatonin, cell membranes, lipid peroxidation, membrane channels, membrane
pores, cell membrane receptors

References

  • Tan DX, Chen LD, Poeggeler B, Manchester LC, Reiter RJ. Melatonin: a potent, endogenous hydroxyl radical scav- enger. Endocrine J, 1: 57-60, 1993.
  • Reiter RJ. Functional pleotrophy of the neurohormone melatonin: antioxidant protection and neuroendocrine regulation. Front Neuroendocrinol, 16: 383-415, 1995.
  • Reiter RJ, Tan DX, Kim SJ, Qi W. Melatonin as a pharma- cological agent against oxidative damage to lipids and DNA. Proc West Pharmacol Soc, 41: 229-236, 1998.
  • Manda K, Ueno M, Anzai K. AFMK, a melatonin metabo- lite, attenuates X-ray-induced oxidative damage to DNA, proteins and lipids in mice. J Pineal Res, 42: 386-393, 2007.
  • Maldonado MD, Murillo-Cabezas F, Terron MP, Flores LJ, Tan DX, Manchester LC, Reiter RJ.The potential of mela- tonin in reducing morbidity-mortality after craniocerebral trauma. J Pineal Res, 42: 1-11, 2007.
  • Tengattini, S, Reiter RJ, Tan DX, Terron MP, Rodella LF. Cardiovascular diseases: protective effects of melatonin. J Pineal Res, 44: 16-25, 2008.
  • Tan DX, Manchester LC, Reiter RJ, Plummer BF, Limson J, Weintraub ST, Qi W. Melatonin directly scavenges hy- drogen peroxide: a potentially new metabolic pathway of melatonin biotransformation. Free Radic Biol Med, 29: 1177-1185, 2000.
  • Tan DX, Manchester LC, Terron MP, Flores LJ, Reiter RJ. One molecule, many derivatives: a never ending interac- tion of melatonin with reactive oxygen and nitrogen spe- cies? J Pineal Res, 42: 28-42, 2007.
  • Pappolla MA, Chyan YJ, Poeggeler B, Frangione B, Wil- son G, Ghiso J, et al. An assessment of the antioxidant and antiamyloidogenic properties of melatonin: implications for Alzheimer’s disease. J Neural Transm, 107: 203-231, 2000.
  • Reiter RJ, Tan DX, Manchester LC, Qi W. Biochemical re- activity of melatonin with reactive oxygen and nitrogen species: a review of the evidence. Cell Biochem Biophys, 34: 237-256, 2001.
  • Reiter RJ, Tan DX, Manchester LC, El-Sawi MR. Melatonin reduces oxidative damage and promotes mitochondrial respiration: implications for aging. Ann NY Acad Sci, 959: 238-250, 2002.
  • Allegra M, Reiter RJ, Tan DX, Gentile C, Tesoriere L, Liv- rea MA. The chemistry of melatonin’s interaction with re- active species. J Pineal Res, 34:1-10, 2003.
  • Hardeland R. Antioxidative protection by melatonin: multiplicity of mechanisms from radical detoxification to radical avoidance. Endocrine, 27: 119-130, 2005.
  • Hardeland R, Backhaus C, Fadavi A. Reactions of the NO redox forms NO+, .NO and HNO (protonated NO-) with the melatonin metabolite N1-acetyl-5-methoxyky- puramine. J Pineal Res, 43: 382-388, 2007.
  • Zavodnik IB, Domanski AV, Lapshina EA, Bryszewska M, Reiter RJ. Melatonin directly scavenges peroxyl and alkoxyl radicals generated in red blood cells and a cell- free system: chemiluminescence measurements and theo- retical calculations. Life Sci, 79: 391-400, 2006.
  • Peyrot N, Ducrocq C. Potential role of tryptophan deriva- tives in stress responses characterized by the generation of reactive oxygen and nitrogen species. J Pineal Res, 45: 235-246. 2008.
  • Tan DX, Reiter RJ, Manchester LC, Yan MT, El-Sawi M, Sainz RM, Mayo JC, Kohen R, Allegra M, Hardeland R. Chemical and physical properties and potential mecha- nisms: melatonin as a broad spectrum antioxidant and free radical scavenger. Curr Topics Med Chem, 2: 181- 198, 2002.
  • Tan DX, Manchester LC, Sainz RM, Mayo JC, Alvarez F, Reiter RJ. Antioxidant strategies in protection against neurodegenerative disorders. Expert Opin Ther Patents, 13: 1513-1542, 2003.
  • Pablos MI, Agapito MT, Gutierrez R, Recio JM, Reiter RJ, Barlow-Walden L, Acuña-Castroviejo D, Menendez- Pelaez A. Melatonin stimulates the activity of the detoxi- fying enzyme glutathione peroxidase in several tissues of chicks. J Pineal Res, 19: 111-115, 1995.
  • Reiter RJ, Tan DX, Osuna C, Gitto E. Actions of melaton- in in the reduction of oxidative stress: a review. J Biomed Res, 7: 444-458, 2000.
  • Rodriguez C, Mayo JC, Sainz RM, Antolín I, Herrera F, Martín V, Reiter RJ. Regulation of antioxidant enzymes: a significant role for melatonin. J Pineal Res, 36: 1-9, 2004.
  • Tomas-Zapico C, Coto-Montes A. A proposed mecha- nism to explain the stimulatory effect of melatonin on antioxidative enzymes. J Pineal Res, 39: 99-104, 2005.
  • Leon J, Escames G, Rodriguez MI, López LC, Tapias V, Entrena A, Camacho E, Carrión MD, Gallo MA, Espinosa A, Tan DX, Reiter RJ, Acuña-Castroviejo D. Inhibition of neuronal nitric oxide synthase activity by N1-acetyl- 5methoxykynuramine, a brain metabolite of melatonin. J Neurochem, 98: 2023-2033, 2006.
  • Urata Y, Honma S, Goto S, Todoroki S, Iida T, Cho S, Hon- ma K, Kondo T. Melatonin induces gamma-glutamyl- cysteine synthase mediated by activator protein-1 in hu- man vascular endothelial cells. Free Radic Biol Med, 27: 838-847, 1999.
  • Winiarska K, Fraczyk T, Molinska D, Drozak J, Bryla J. Melatonin attenuates diabetes-induced oxidative stress in rabbits. J Pineal Res, 40: 168-176, 2006.
  • Sainz RM, Reiter RJ, Tan DX, Roldan F, Natarajan M, Quiros I, Hevia D, Rodriguez C, Mayo JC. Critical role of glutathione in melatonin enhancement of tumor necrosis factor and ionizing radiation-induced apoptosis in pros- tate cancer cells in vitro. J Pineal Res, 45: 258-270, 2008.
  • Okatani Y, Wakasuki A, Reiter RJ. Hepatic mitochondri- al dysfunction in senescence-accelerated mice: correction by long-term, orally administered physiological levels of melatonin. J Pineal Res, 33: 127-133, 2002.
  • Martin M, Macias M, Escames G, Reiter RJ, Agapito MT, Ortiz GG, Acuña-Castroviejo D. Melatonin-induced in- creased activity of the respiratory complexes I and IV can prevent mitochondrial damage induced by ruthe- nium red in vivo. J Pineal Res, 28: 242-248, 2000.
  • Leon J, Acuna-Castroviejo D, Escames G, Tan DX, Re- iter RJ. Melatonin mitigates mitochondrial malfunction. J Pineal Res, 38: 1-9, 2005.
  • Reiter RJ, Paredes SD, Korkmaz A, Jou MJ, Tan DX. Me- latonin combats molecular terrorism at the mitochondri- al level. Interdisc Toxicol, 1: 137-149, 2008.
  • Jou MJ, Peng TI, Yu PZ, Jou SB, Reiter RJ, Chen JY, Wu HY, Chen CC, Hsu LF. Melatonin protects against com- mon deletion of mitochondria DNA-augmented mito- chondrial oxidative stress and apoptosis. J Pineal Res, 43: 389-403, 2007.
  • Jou, MJ, Peng TI, Reiter RJ, Jou SB, Wu HY, Wen ST. Visualization of the antioxidative effects of melatonin at the mitochondrial level during oxidative stress-induced apoptosis of rat brain astrocytes. J Pineal Res, 37: 55-70, 2004.
  • Cervantes M, Morali G, Letechipia-Vallejo G. Melatonin and ischemia-reperfusion injury. J Pineal Res, 45: 1-7, 2008.
  • De Filippis D, Iuvone T, Esposito G, Steardo L, Arnold GH, Paul AP, De Man Joris G, De Winter Benedicte Y. Melatonin reverses lipopolysaccharide-induced gastro- intestinal mobility disturbances through the inhibition of oxidative stress. J Pineal Res, 44: 45-51, 2008.
  • Tamura H, Takasaki A, Miwa I, Taniguchi K, Maekawa R, Asada H, Taketani T, Matsuoka A, Yamagata Y, Shi- mamura K, Morioka H, Ishikawa H, Reiter RJ, Sugino N. Oxidative stress impairs oocyte quality and melatonin protects oocytes from free radical damage and improves fertilization rate. J Pineal Res, 44: 280-287, 2008.
  • Gitto E, Pelligrino S, Gitto P, Barberi I, Reiter RJ. Oxida- tive stress of the newborn in the pre-and post-natal pe- riod and the clinical utility of melatonin. J Pineal Res, 46: 128-139, 2009.
  • Gitto E, Karbownik M, Reiter RJ, Tan DX, Cuzzocrea S, Chiurazzi P, Cordaro S, Corona G, Trimarchi G, Barberi I. Effects of melatonin treatment in septic newborns. Pediatr Res, 50: 756-760, 2000.
  • Fulia F, Gitto E, Cuzzocrea S, Reiter RJ, Dugo L, Gitto P, Barberi S, Cordaro S, Barberi I. Increased levels of malondialdehyde and nitrite/nitrate in the blood of as- phyxiated newborns: reduction by melatonin. J Pineal Res, 31: 343-349, 2001.
  • Kucukakin B, Lykkesfeldt J, Nielsen HJ, Reiter RJ, Rosen- berg J, Gogenur I. Utility of melatonin to treat surgical stress after major vascular surgery – a safety study. J Pin- eal Res, 44: 426-431, 2008.
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There are 80 citations in total.

Details

Primary Language English
Journal Section Articles
Authors

Russel Reiter This is me

Lorena Fuentes-broto This is me

Sergio Paredes This is me

Dun-xian Tan This is me

Joaquin Garcia This is me

Publication Date March 3, 2014
Published in Issue Year 2010 Volume: 14 Issue: 1

Cite

APA Reiter, R., Fuentes-broto, L., Paredes, S., Tan, D.-x., et al. (2014). Melatonin and the pathophysiology of cellular membranes. Marmara Pharmaceutical Journal, 14(1), 1-9. https://doi.org/10.12991/mpj.06923
AMA Reiter R, Fuentes-broto L, Paredes S, Tan Dx, Garcia J. Melatonin and the pathophysiology of cellular membranes. J Res Pharm. March 2014;14(1):1-9. doi:10.12991/mpj.06923
Chicago Reiter, Russel, Lorena Fuentes-broto, Sergio Paredes, Dun-xian Tan, and Joaquin Garcia. “Melatonin and the Pathophysiology of Cellular Membranes”. Marmara Pharmaceutical Journal 14, no. 1 (March 2014): 1-9. https://doi.org/10.12991/mpj.06923.
EndNote Reiter R, Fuentes-broto L, Paredes S, Tan D-x, Garcia J (March 1, 2014) Melatonin and the pathophysiology of cellular membranes. Marmara Pharmaceutical Journal 14 1 1–9.
IEEE R. Reiter, L. Fuentes-broto, S. Paredes, D.-x. Tan, and J. Garcia, “Melatonin and the pathophysiology of cellular membranes”, J Res Pharm, vol. 14, no. 1, pp. 1–9, 2014, doi: 10.12991/mpj.06923.
ISNAD Reiter, Russel et al. “Melatonin and the Pathophysiology of Cellular Membranes”. Marmara Pharmaceutical Journal 14/1 (March 2014), 1-9. https://doi.org/10.12991/mpj.06923.
JAMA Reiter R, Fuentes-broto L, Paredes S, Tan D-x, Garcia J. Melatonin and the pathophysiology of cellular membranes. J Res Pharm. 2014;14:1–9.
MLA Reiter, Russel et al. “Melatonin and the Pathophysiology of Cellular Membranes”. Marmara Pharmaceutical Journal, vol. 14, no. 1, 2014, pp. 1-9, doi:10.12991/mpj.06923.
Vancouver Reiter R, Fuentes-broto L, Paredes S, Tan D-x, Garcia J. Melatonin and the pathophysiology of cellular membranes. J Res Pharm. 2014;14(1):1-9.

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