Τόμος 25 (2011) – Τεύχος 3 – Άρθρο 3 – Review of Clinical Pharmacology and Pharmacokinetics-Διεθνής Έκδοση – Volume 25 (2011) – Issue 3 – Article 3 – Review of Clinical Pharmacology and Pharmacokinetics -International Edition

1. Division of Aesthetics and Cosmetology, School of Health and Caring Professions, Technological Educational Institution of Athens, Ag. Spyridonos Str., GR-12210 Egaleo, Athens, Greece

2. Department of Biology, National and Kapodistrian University of Athens, Panepistimioupolis Zografou Gr-15784, Athens, Greece

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2. Coesel S., Obornik M., Varela J., Falciatore A., Bowler C.: Evolutionary origins and functions of the carotenoid biosynthetic pathway in marine diatoms. PLoS ONE: 3(8): e2896 (2008)

3. Agar N., Halliday G., Barnetson R., Ananthaswamy H., Wheeler M., Jones A.: The basal layer in human squamous tumors harbors more UVA than UVB fingerprint mutations: A role for UVA in human skin carcinogenesis. Proc. Natl. Acad. Sci. USA 101: 4954-4959 (2004)

4. Ryu B., Qian Z.J., Kim M.M., Nam K.W., Kim S.K.: Anti-photoaging activity and inhibition of matrixmetalloproteinase (MMP) by marine red alga, Corallina pilulifera methanol extract. Radiat. Phys. Chem. 78: 98-105 (2009)

5. Kondo S.: The roles of cytokines in photoaging. J. Dermatol. Sci. 23: 30-36 (2002)

6. Rittie L., Fisher G.J.: UV-light-induced signal cascades and skin aging. Ageing Res. Rev. 1: 705-720 (2002)

7. Kehrer J.P.: Free radicals as mediators of tissue injury and disease. CRC Crit. Rev. Toxicol. 23: 21-48 (1993)

8. Aruoma O.I.: Nutrition and health aspects of free radicals and antioxidant. Food Chem. Toxicol. 62: 671-683 (1994)

9. Fiers W., Bevaert R., Declercq W., Vandenabeele P.: More than one way to die: Apoptosis and necrosis and reactive oxygen damage. Oncogene 18: 7719-7730 (1999)

10. Record I.R., Dreosti I.E., Konstantinopoulos M., Buckley R.A.: The influence of topical and systemic vitamin E on ultraviolet light-induced skin damage in hairless mice. Nutr. Cancer 16: 219-226 (1991)

11. Kawaguchi Y., Tanaka H., Okada T., Konishi H., Takahashi M., Ito M., Asai J.: The effects of ultraviolet A and reactive oxygen species on the mRNA expression of 72-kDa type IV collagenase and its tissue inhibitor in cultured human dermal fibroblasts. Arch. Dermatol. Res. 288: 39-44 (1996)

12. Bode W., Fernandez-Catalan C., Tschesche H., Grams F., Nagase H., Maskos K.: Structural properties of matrix metalloproteinases. Cell Mol. Life Sci. 55: 639-652 (1999)

13. Kang S., Chung J.H., Lee J.H., Fisher G.J., Wan Y.S., Duell E.A., Voorhees J.J.: Topical Nacetyl cysteine and genistein prevent ultraviolet-light-induced signaling that leads to photoaging in human skin in vivo. J. Invest. Dermatol. 120: 835-841 (2003)

14. Inomata S., Matsunaga Y., Amano S., Takada K., Kobayashi K., Tsunenaga M., Nishiyama T., Kohno Y., Fukuda M.: Possible involvement of gelatinases in basement membrane damage and wrinkle formation in chronically ultraviolet B-exposed hairless mouse. J. Invest. Dermatol. 120: 128-134 (2003)

15. Sinha R.P., Klisch M., Gröniger A., Häder D.P.: Ultra-violet-absorbing/screening substances in cyanobacteria, phytoplankton and macroalgae, J. Photochem. Photobiol. B Biol. 47: 83-94 (1998)

16. Sinha R.P., Singh S.P., Häder D.P.: Database on mycosporines and mycosporine-like amino acids (MAAs) in fungi, cyanobacteria, macroalgae, phytoplankton and animals. J. Photochem. Photobiol. B Biol. 89: 29-35 (2007)

17. Edwards H.G.M., Moeller R., Villar S.E.J., Horneck G., Stackebrandt E.: Raman: spectroscopic study of the photoprotection of extremophilic microbes against ultraviolet radiation. Int. J. Astrobiol. 5: 313-318 (2006)

18. Kumar R., Patel D.D., Bansal D.D., Mishra S., Mo-hammed S., Arora R., Sharma A., Sharma R.K., Tripathi R.P.: Extremophiles: Sustainable resource of natural compounds-extremolytes. In: Sustainable Biotechnology, Sources of Renewable Energy (Singh O.V., Harvey S.P., eds). Pp. 279-294, Springer: Dordrecht, Netherlands, 2009

19. Cahyana A.H., Shuto Y., Kinoshita Y.: Pyropheo-phytin A as an antioxidative substance from the marine alga, Arame (Eicenia bicyclis). Biosci. Biotechnol. Agro-chem. 56: 1533-1535 (1992)

20. Yan X., Chuda Y., Suzuki M., Nagata T.: Fucoxan-thin as the major antioxidant in Hijikia fusiformis, a common edible seaweed. Biosci. Biotechnol. Biochem. 63: 605-607 (1999)

21. Kang H.S., Chung H.Y., Jung H.A., Son B.W., Choi J.S.: A new phlorotannins from the brown alga Ecklonia stolonifera. Chem. Pharm. Bull. 51: 1012-1014 (2003)

22. Heo S.J., Ko S.C., Cha S.H., Kang D.H., Park H.S., Choi Y.U., Kim D., Jung W.K., Jeon Y.J.: Effect of phlorotannins isolated from Ecklonia cava on melanogenesis and their protective effect against photo-oxidative stress induced by UV-B radiation. Toxicol. In Vitro 23: 1123-1130 (2009)

23. Hur S., Lee H., Kim Y., Lee B.H., Shin J., Kim T.Y.: Sargaquinoic acid and sargachromenol, extracts of Sargassum sagamianum, induce apoptosis in HaCaT cells and mice skin: Its potentiation of UVB-induced apoptosis. Eur. J. Pharmacol. 582: 1-11 (2008)

24. Tsang C.K., Ina A., Goto T., Kamei Y.: Sargachromenol, a novel nerve growth factorpotentiating substance isolated from Sargassum macrocarpum, pro-motes neurite outgrowth and survival via distinct signaling pathways in PC12D cells. Neuroscience 132: 633-643 (2005)

25. De la Coba F., Aguilera J., de Gálvez M.V., Álvarez M., Gallego E., Figueroa F.L., Herrera E.: Prevention of the ultraviolet effects on clinical and histopathological changes, as well as the heat shock protein-70 expression in mouse skin by topical application of algal UV-absorbing compounds. J. Dermatol. Sci. 55: 161-169 (2009)

26. Lyons N.M., O’Brien N.M.: Modulatory effects of an algal extract containing astaxanthin on Airradiated cells in culture. J. Dermatol. Sci. 30: 73-84 (2002)

27. Heo S.J., Jeon Y.J.: Protective effect of fucoxanthin isolated from Sargassum siliquastrum on UV-B induced cell damage. J. Photochem. Photobiol. B Biol. 95: 101-107 (2009)

28. Bradbury J.: Nature’s Nanotechnologists: Unveiling the secrets of diatoms. Public Lib. Sci. Biol. 2: 1512-1515 (2004)

29. Li S., Nosenko T., Hackett J.D., Bhattacharya D.: Phylogenomic analysis identifies red algal genes of endosymbiotic origin in the chromalveolates. Mol. Biol. Evol. 23: 663-674 (2006)

30. Patron N.J., Rogers M.B., Keeling P.J.: Gene re-placement of fructose-1,6-bisphosphate aldolase sup-ports the hypothesis of a single photosynthetic ancestor of chromalveolates. Eukaryo. Cell. 3: 1169-1175 (2004)

31.Yoon H.S., Hackett J.D., Ciniglia C., Pinto G., Bhattacharya D.: A molecular timeline for the origin of photosynthetic eukaryotes. Mol. Biol. Evol. 21: 809-818 (2004)

32. Cavalier-Smith T.: Eukaryote kingdoms: seven or nine? Biosystems 14: 461-481 (1981)

33. MacIntyre H.L., Kana T.M., Geider R.J.: The effect of water motion on short-term rates of photosynthesis by marine phytoplankton. Trends Plant Sci. 5: 12-17 (2000)

34. Strzepek R.F., Harrison P.J.: Photosynthetic architecture differs in coastal and oceanic diatoms. Nature 431: 689-692 (2004)

35. Wagner H., Jakob T., Wilhelm C.: Balancing the energy flow from captured light to biomass under fluctuating light conditions. New Phytol. 169: 95-108 (2006)

36. Ruban A., Lavaud J., Rousseau B., Guglielmi G., Horton P., et al.: The super-excess energy dissipation in diatom algae: comparative analysis with higher plants. Photosynth. Res. 82: 165-175 (2004)

37. Lavaud J., Rousseau B., Etienne A.L.: Enrichment of the light-harvesting complex in diadinoxanthin and implications for the nonphotochemical fluorescence quenching in diatoms. Biochemistry 42: 5802-5808 (2003)

38. Falkowski P.G., Laroche J.: Acclimation to spectral irradiance in algae. J. Phycol. 27: 8-14 (1991)

39. Muller P., Li X.P., Niyogi K.K.: Non-photochemical quenching. A response to excess light energy. Plant Physiol. 125: 1558-1566 (2001)

40. Holt N.E., Fleming G.R., Niyogi K.K.: Toward an understanding of the mechanism of nonphotochemical quenching in green plants. Biochemistry 43: 8281-8289 (2004)

41. Niyogi K.K., Li X.P., Rosenberg V., Jung H.S.: Is PsbS the site of non-photochemical quenching in photosynthesis? J. Exp. Bot. 56: 375-382 (2005)

42. Hager A.: Lichtbedingte pH-erniedrigung in einem chloroplastem-kompatiment als ursache der enzymatische violaxanthin zu Zeaxanthinumwandlung; Beziehungen zur photophosphorylierung. Planta 89: 224-243 (1969)

43. Olaizola M., La Roche J., Kolber Z., Falkowski P.: Non-photochemical fluorescence quenching and the diadinoxanthin cycle in a marine diatom. Photosynth. Res. 41: 357-370 (1994)

44. Zudaire L., Roy S.: Photoprotection and long-term acclimation to UV radiation in the marine diatom Thalassiosira weissflogii. J. Photochem. Photobiol. B Biol. 62: 26-34 (2001)

45. Hasle G., Syvertsen E.E.: Marine diatoms. In: Identifying Marine Diatoms and Dinoflagellates (Tomas C.R., ed.) Pp. 5-385, Academic Press: San Diego, CA, USA, 1996

46. Helbling E.W., Chalker B.E., Dunlap W.C., Holm-Hansen, O., Villafañe V.E.: Photoacclimation of Antarctic marine diatoms to solar ultraviolet radiation. J. Exp. Mar. Biol. Ecol. 204: 85-101 (1996)

47. El-Sayed S.Z., Stephens F.C., Bidigare R.R., Ondrusek M.E.: Effect of ultraviolet radiation on Antarctic marine phytoplankton. In: 5th SCAR Symposium on the Ecological Changes and the Conservation of Antarctic Ecosystems (Kerry K.R., Hempel G., Eds). Pp. 379-385, Springer-Verlag: Berlin, Germany, 1990

48. Karentz D.: Ultraviolet tolerance mechanisms in Antarctic marine organisms, in Ultraviolet radiation in Antarctica: Measurements and biological effects. Antarctic Res. Ser. 62: 93-110 (1994)

49. Hannach G., Sigleo A.C.: Photoinduction of UV-absorbing compounds in six species of marine phytoplankton. Mar. Ecol. Prog. Ser. 174: 207-222 (1998)

50. Torres A., Hochberg M., Pergament I., Smoum R., Niddam V., Dembitsky V.M., Temina M., Dor I., Lev O., Srebnik M., Enk C.D.: A new UV-B absorbing mycosporine with photo protective activity from the lichenized ascomycete Collema cristatum. Eur. J. Biochem. 271: 780-784 (2004)

51. Kogej T., Gostincar C., Volkmann M., Gorbushina A.A., Gunde-Cimerman N.: Mycosporines in extremophilic fungi-novel complementary osmolytes? Environ. Chem. 3: 105-110 (2006)

52. Muller K.: Pharmaceutically relevant metabolites from lichens. Appl. Microbiol. Biotechnol. 56: 9-16 (2001)

53. Huneck S.: New results on the chemistry of lichen substances. Fortschritte der Chemie Organischer Naturstoffe 81: 1-276 (2001)

54. Geng J., Yu S.B., Wan X., Wang X.J., Shen P., Zhou, P., Chen X.D.: Protective action of bacterial melanin against DNA damage in full UV spectrums by a sensitive plasmid-based non-cellular system. J. Biochem. Bio-phys. Meth. 70: 1151-1155 (2008)

55. Stewart W.D.P.: Some aspects of structure and func-tion in N2-fixing cyanobacteria. Annu. Rev. Microbiol. 34: 497-536 (1980)

56. De Marsac N.T., Houmard J.: Adaptation of cyano-bacteria to environmental stimuli: New steps towards molecular mechanisms. FEMS Microbiol. Rev. 104: 119-190 (1993)

57. Haider D.P.: Phototensory behavior in prokaryotes. Microbiol. Rev. 51: 1-21 (1987)

58. Bedout B.M., Garcia-Pichel F.: UV-B induced vertical migrations of cyanobacteria in a microbial mat. Appl. Environ. Microbiol. 61: 4215-4222 (1995)

59. Burton G.W., Ingold K.U.: β-Carotene: An unusual type of lipid antioxidant. Science 224: 569-573 (1984)

60. Vincent W.F., Quesada A.: Ultraviolet radiation effects on cyanobacteria: Implication for Antarctic microbial ecosystems. In: Ultraviolet Radiation in Antarctica: Measurements and Biological Effects (Weiler C.S., Penhale P.A., eds). Antarctic Research Series, American Geophysical Union: Washington, DC, USA 62: 111-124 (1994)

61. Kim S.T., Sancar A.: Photorepair of nonadjacent pyrimidine dimmers by DNA photolyase. Photochem. Photobiol. 61: 171-174 (1995)

62. Christopher D.A., Mullet J.E.: Separate photosensory pathways coregulate blue light/ultraviolet-A-activated psbD-psbC transcription and light induced D2 and CP43 degradation in barley (Hordeum vulgare) chloroplasts. Plant Physiol. 104: 1119-1129 (1994)

63. De Marsac N.T.: Occurrence and nature of chromatic adaptation in cyanobacteria. J. Bacteriol. 130: 82-91 (1997)

64. Garcia-Pichel F., Wingard C.E., Castenholz R.W.: Evidence regarding the UV sunscreen role of a mycosporine-like compound in the cyanobacterium Gloe-ocapsa sp. Appl. Environ. Microbiol. 59: 170-176 (1993)

65. Chen H.Y., Chu X., Yan C.L., Chen X.H., Sun M., Wang Y.J., Wang C.B., Yu W.G.: Polypeptide from Chlamys farreri attenuates murine thymocytes damage induced by ultraviolet B. Acta Pharmacol. Sin. 28: 1665-1670 (2007)

66. Li J.L., Liu N., Chen X.H., Sun M., Wang C.B.: Inhibition of UVA-induced apoptotic signalling pathway by polypeptide from Chlamys farreri in human HaCaT keratinocytes. Radiat. Environ. Biophys. 46: 263-268 (2007)

67. Xing Y.X., Li P., Miao Y.X., Du W., Wang C.B.: Involvement of ROS/ASMase/JNK signalling pathway in inhibiting UVA-induced apoptosis of HaCaT cells by poly-peptide from Chlamys farreri. Free Radic. Res. 42: 12-19 (2008)

68. Bandaranayake W.M., des Rocher A.: Role of secondary metabolites and pigments in the epidermal tissues, ripe ovaries, viscera, gut contents and diet of the sea cucumber (Holothuria atra). Mar. Biol. 133: 163-169 (1999)

69. Oyamada C., Kaneniwa M., Ebitani K., Murata M., Ishihara, K.: Mycosporine-like amino acids extracted from scallop (Patinopecten yessoensis) ovaries: UV protection and growth stimulation activities on human cells. Mar. Biotechnol. 10: 141-150 (2008)