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DOI 10.3969/j.issn.1673-4254.2017.01.06

Медицинская библиотека · Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2017

[Establishment of a SD rat model of vulvar lichen simplex chronicus and detection of the expression of protease activated receptor 2].

Yang Huan, Fu Zhen-Hua, Tang Hua-Jun, Li Cheng-Zhi

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Аннотация

OBJECTIVE

To establish a SD rat model of vulvar lichen simplex chronicus (LSC) and investigate the expression of protease activated receptor 2 (PAR2) in the genital skin.

METHODS

Seventy female SD rats were randomly divided into group A (blank control group, n=10), group B (with application of acetone solution 3 times per week for 10 weeks, n=10), group C (with chronic mechanical irritation 3 times per week for 10 weeks, n=10), and group D (with topical treatment with 0.5= 7,12-Dimethylbenzanthracene [DMBA] in acetone solution and chronic mechanical irritation 3 times per week for 10 weeks, n=40). The changes of the genital skin changes were observed regularly and the expression of PAR2 in groups A and D was detected with immunohistochemistry, Western blotting and qRT-PCR.

RESULTS

In group D, LSC occurred in 23 rats (57.5=) at 8 weeks and in 38 rats (95=) at 10 weeks; 8 rats (20=) showed papilloma at 12 weeks. Acetone treatment or chronic mechanical irritation did not cause LSC in the rats. Immunohistochemistry, Western blotting and qRT-PCR showed significantly increased expressions of PAR2 in group D at both the protein and mRNA levels as compared with those in group A (P<0.05).

CONCLUSION

0.5= DMBA in acetone solution along with chronic mechanical irritation can induce LSC in female SD rats, and PAR2 is closely related with the occurrence and progression of LSC.

Для цитирования: Yang Huan, Fu Zhen-Hua, Tang Hua-Jun, Li Cheng-Zhi. [Establishment of a SD rat model of vulvar lichen simplex chronicus and detection of the expression of protease activated receptor 2].. Nan fang yi ke da xue xue bao = Journal of Southern Medical University. 2017. DOI: 10.3969/j.issn.1673-4254.2017.01.06.

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