Mouse model of UVB-induced hyperpigmentation and SF treatment.

MK Michelle L. Kerns
RM Robert J. Miller
MM Momina Mazhar
AB Angel S. Byrd
NA Nathan K. Archer
BP Bret L. Pinkser
LL Lance Lew
CD Carly A. Dillen
RW Ruizhi Wang
LM Lloyd S. Miller
AC Anna L. Chien
SK Sewon Kang
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For topical SF treatment, 6-month-old WT and Nrf2–/– C57BL/6 male mice were exposed to 80 mJ/cm2 UVB (range 290–315 nm) using a Philips TL Broadband UVB lamp (TL 20W/12 RS SLV/25, Philips) in ventilated cabinets equipped with UVB lamps once daily 5 times a week for 4 weeks. For the next 4 weeks of UVB treatment, just prior to the UVB treatment, mice were anesthetized (2% isoflurane), and SF (1 μM; LKT Laboratories Inc.) was topically applied to the right ear (UVB+SF), while the left ear received either vehicle oil (jojoba oil, MP Biomedical LLC) (UVB+Oil) or no topical treatment (UVB). For the topical SF preventative treatment, 6-week-old WT, Nrf2–/–, or K14-Cre-ERT2IL-6Rαfl/fl (previously treated with tamoxifen [1 mM] i.p. daily for 5 days) C57BL/6 male mice were exposed to 80 mJ/cm2 UVB daily 5 times a week for 4 weeks and, in the anesthetized mice just prior to UVB exposure, topical SF was applied to the right ear (UVB+SF), while the left ear received either vehicle oil (jojoba oil, MP Biomedical LLC) (UVB+Oil) or no topical treatment (UVB). In all experiments, an additional Un control group of age-matched male mice that received no UVB treatment and no topical treatment was included.

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