TY - JOUR
T1 - Inhibitory effects of dietary spirulina platensis on UVB-induced skin inflammatory responses and carcinogenesis
AU - Yogianti, Flandiana
AU - Kunisada, Makoto
AU - Nakano, Eiji
AU - Ono, Ryusuke
AU - Sakumi, Kunihiko
AU - Oka, Sugako
AU - Nakabeppu, Yusaku
AU - Nishigori, Chikako
N1 - Funding Information:
This work was supported by Grant-in-Aid 19390296 from the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT), Grant-in-Aid from the Program for “Raising Young Research Leaders in Biomedical Science of Kobe University”, the Foundation of International Dermatology of Charitable Trust, Global Centre of Excellence Program for “Education and Research on Signal Transduction Medicine in the Coming Generation” (GCOE Program “Signal”) of MEXT, the Kanae Foundation for the Promotion of Medical Science, and the Cosmetology Research Foundation. We thank DIC LIFTECH (Tokyo, Japan) for kindly providing us the S. platensis and PCB powder.
PY - 2014/1/1
Y1 - 2014/1/1
N2 - Reactive oxygen species produced in response to UVR are important in skin tumor development. We have previously reported that deficiency of the Ogg1 gene, encoding the repair enzyme for 8-oxo-7,8-dihydroguanine (8-oxoG), increases skin tumor incidence in mice upon repetitive UVB exposure and modulation of UVB-induced inflammatory response. Spirulina platensis is used as a human food supplement because it contains abundant nutritional and antioxidant components. Therefore, we investigated the inhibitory effects of S. platensis on UVB-induced skin tumor development in Ogg1 knockout-(KO) mice and the wild-type (WT) counterpart. Dietary S. platensis suppressed tumor induction and development in both genotypes compared with our previous data without S. platensis. Induction of erythema and ear swelling, one of the hallmarks of UVB-induced inflammatory responses, was suppressed in the skin of Ogg1-KO mice and albino hairless mice fed with dietary S. platensis. Compared with untreated mice, S. platensis-administered mice showed significantly reduced 8-oxoG formation in the skin after UVB exposure. Moreover, we found that S. platensis effectively downregulated the signal proteins p38 mitogen-activated protein kinase, stress-activated protein kinase/c-Jun N-terminal kinase, and extracellular signal-regulated kinase after UVB exposure especially in Ogg1-KO mice. Our results suggest that S. platensis exerts antitumor effects against UVB irradiation in the skin through its anti-inflammatory and antioxidant effects.
AB - Reactive oxygen species produced in response to UVR are important in skin tumor development. We have previously reported that deficiency of the Ogg1 gene, encoding the repair enzyme for 8-oxo-7,8-dihydroguanine (8-oxoG), increases skin tumor incidence in mice upon repetitive UVB exposure and modulation of UVB-induced inflammatory response. Spirulina platensis is used as a human food supplement because it contains abundant nutritional and antioxidant components. Therefore, we investigated the inhibitory effects of S. platensis on UVB-induced skin tumor development in Ogg1 knockout-(KO) mice and the wild-type (WT) counterpart. Dietary S. platensis suppressed tumor induction and development in both genotypes compared with our previous data without S. platensis. Induction of erythema and ear swelling, one of the hallmarks of UVB-induced inflammatory responses, was suppressed in the skin of Ogg1-KO mice and albino hairless mice fed with dietary S. platensis. Compared with untreated mice, S. platensis-administered mice showed significantly reduced 8-oxoG formation in the skin after UVB exposure. Moreover, we found that S. platensis effectively downregulated the signal proteins p38 mitogen-activated protein kinase, stress-activated protein kinase/c-Jun N-terminal kinase, and extracellular signal-regulated kinase after UVB exposure especially in Ogg1-KO mice. Our results suggest that S. platensis exerts antitumor effects against UVB irradiation in the skin through its anti-inflammatory and antioxidant effects.
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U2 - 10.1038/jid.2014.188
DO - 10.1038/jid.2014.188
M3 - Article
C2 - 24732403
AN - SCOPUS:84922395153
SN - 0022-202X
VL - 134
SP - 2610
EP - 2619
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
IS - 10
ER -