Tualang Honey Protects Keratinocytes from Ultraviolet Radiation-Induced Inflammation and DNA Damage

被引:35
作者
Ahmad, Israr [1 ,2 ]
Jimenez, Hugo [1 ,2 ]
Yaacob, Nik Soriani [4 ]
Yusuf, Nabiha [1 ,2 ,3 ,4 ]
机构
[1] Vet Affairs Med Ctr, Dept Dermatol, Birmingham, AL USA
[2] Vet Affairs Med Ctr, Skin Dis Res Ctr, Birmingham, AL USA
[3] Univ Alabama Birmingham, Ctr Comprehens Canc, Birmingham, AL 35294 USA
[4] Univ Sains Malaysia, Sch Med Sci, George Town, Malaysia
关键词
NF-KAPPA-B; HUMAN SKIN; IN-VITRO; MOUSE; EXPRESSION; CELLS; QUANTIFICATION; IDENTIFICATION; ACTIVATION; EXPOSURE;
D O I
10.1111/j.1751-1097.2012.01100.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Malaysian tualang honey possesses strong antioxidant and anti-inflammatory properties. Here, we evaluated the effect of tualang honey on early biomarkers of photocarcinogenesis employing PAM212 mouse keratinocyte cell line. Keratinocytes were treated with tualang honey (1.0%, v/v) before a single UVB (150 mJ cm-2) irradiation. We found that the treatment of tualang honey inhibited UVB-induced DNA damage, and enhanced repair of UVB-mediated formation of cyclobutane pyrimidine dimers and 8-oxo-7,8-dihydro-2'-deoxyguanosine. Treatment of tualang honey inhibited UVB-induced nuclear translocation of NF-?B and degradation of I?Ba in murine keratinocyte cell line. The treatment of tualang honey also inhibited UVB-induced inflammatory cytokines and inducible nitric oxide synthase protein expression. Furthermore, the treatment of tualang honey inhibited UVB-induced COX-2 expression and PGE2 production. Taken together, we provide evidence that the treatment of tualang honey to keratinocytes affords substantial protection from the adverse effects of UVB radiation via modulation in early biomarkers of photocarcinogenesis and provide suggestion for its photochemopreventive potential.
引用
收藏
页码:1198 / 1204
页数:7
相关论文
共 35 条
[1]   Suppression of ultraviolet B exposure-mediated activation of NF-κB in normal human keratinocytes by resveratrol [J].
Adhami, VM ;
Afaq, F ;
Ahmad, N .
NEOPLASIA, 2003, 5 (01) :74-82
[2]   Photochemoprevention of ultraviolet B signaling and photocarcinogenesis [J].
Afaq, F ;
Adhami, VM ;
Mukhtar, H .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2005, 571 (1-2) :153-173
[3]  
Ainul Hafiza A. H., 2005, SAINS MALAYS, V34, P17
[4]   Evaluation of the phenolic contents and antioxidant capacities of two Malaysian floral honeys [J].
Aljadi, AM ;
Kamaruddin, MY .
FOOD CHEMISTRY, 2004, 85 (04) :513-518
[5]   In situ profiling and quantification of cytokines released during ultraviolet B-induced inflammation by combining dermal microdialysis and protein microarrays [J].
Averbeck, M ;
Beilharz, S ;
Bauer, M ;
Gebhardt, C ;
Hartmann, A ;
Hochleitner, K ;
Kauer, F ;
Voith, U ;
Simon, JC ;
Termeer, C .
EXPERIMENTAL DERMATOLOGY, 2006, 15 (06) :447-454
[6]   Photoimmunology, DNA repair and photocarcinogenesis [J].
Berneburg, M ;
Krutmann, J .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2000, 54 (2-3) :87-93
[7]   Prevention of non-melanoma skin cancer by targeting ultraviolet-B-light signalling [J].
Bowden, GT .
NATURE REVIEWS CANCER, 2004, 4 (01) :23-35
[8]  
CAMPBELL C, 1993, CANCER RES, V53, P2697
[9]   Ultraviolet B Radiation Activates NF-κB and Induces iNOS Expression in HR-1 Hairless Mouse Skin: Role of IκB Kinase-β [J].
Chang, Eun-Jin ;
Kundu, Joydeb Kumar ;
Liu, Lijia ;
Shin, Jun-Wan ;
Surh, Young-Joon .
MOLECULAR CARCINOGENESIS, 2011, 50 (04) :310-317
[10]  
Che Ghazali F., 2009, Annals of Microscopy, V9, P93