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. 2016 Apr;39(2):534-42.
doi: 10.1007/s10753-015-0277-z.

Involvement of Prokineticin 2 and Prokineticin Receptor 1 in Lipopolysaccharide-Induced Testitis in Rats

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Involvement of Prokineticin 2 and Prokineticin Receptor 1 in Lipopolysaccharide-Induced Testitis in Rats

Biao Chen et al. Inflammation. 2016 Apr.

Abstract

Prokineticin 2, a newly discovered proinflammatory peptide, has been amply evidenced to be involved in the occurrence and progress of local and systematical inflammation. Although the presence of Prokineticn 2 in mammal testis has been documented clearly, research targeting the involvement of prokineticin 2 in testicular pathology, especially testitis, is rather scarce. Employing a lipopolysaccharide-induced testitis rat model, we for the first time demonstrated the expression and upregulation of prokineticin 2 in orchitis at several levels. Our effort also addressed the differential expression patterns of prokineticin 2 and interleukin-1β, a key inflammation indicator, during testitis suggesting Prokineticn 2 serves more than a proinflammatory factor in the context of testitis. Given one of the cognate receptors of prokineticin 2, prokineticin receptor 1 (PKR1) was also significantly upregulated in orchitis as discussed in the current study, it is very likely that PK2/PKR1 signaling contribute to the development of inflammation-related testicular diseases.

Keywords: BV8; male infertility; orchitis; prokineticin; testitis.

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References

    1. Biochem Biophys Res Commun. 2002 Apr 26;293(1):396-402 - PubMed
    1. J Clin Endocrinol Metab. 2004 May;89(5):2463-9 - PubMed
    1. Mol Pharmacol. 2004 Mar;65(3):582-8 - PubMed
    1. J Reprod Immunol. 2002 Oct-Nov;57(1-2):19-34 - PubMed
    1. Am J Physiol Regul Integr Comp Physiol. 2005 Jun;288(6):R1744-55 - PubMed

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