Bradykinin system is involved in endometriosis-related pain through endothelin-1 production

Yoshino O, O Yoshino, Osamu Yoshino, K Yamada-Nomoto, Kaori Yamada‐Nomoto, Yamada-Nomoto K, Mutsumi Kobayashi, M Kobayashi, Kobayashi M, Andoh T, Tsugunobu Andoh, T Andoh, Makiko Hongo, Hongo M, M Hongo, Y Ono, Ono Y, Yosuke Ono, A Hasegawa-Idemitsu, A. Hasegawa‐Idemitsu, Hasegawa-Idemitsu A, Atsushi Sakai, A Sakai, Sakai A, Yutaka Osuga, Osuga Y, Y Osuga, S. Saito, Shigeru Saito, Saito S
European journal of pain (London, England) · 2017 · vol. 22(3) , pp. 501–510 · doi:10.1002/ejp.1133 · PMID:29034546 · W2765850679
Lab / animal OA: closed CC0 ⤵ 13 in-corpus citations
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The bradykinin system and endothelin-1 production are involved in endometriosis-related pain, with bradykinin activation inducing endothelin-1 expression in endometriotic stromal cells.

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Abstract

BACKGROUND: Endometriosis is a gynaecological disease exhibiting severe pelvic pain, but the mechanism of pain production remains unknown. Bradykinin (BK) is known as an inflammatory mediator, and shows elevated levels in inflammatory diseases such as rheumatoid arthritis. In the present study, we evaluated whether BK is involved in endometriosis-related pain. METHODS: Endometriotic lesions were used for immunohistochemistry. Primary cultures of endometriotic stromal cells (ESC) were stimulated with IL-1β and/or BK. Quantitative RT-PCR was used to evaluate the mRNA expressions of BK receptors (BKR) and endothelin-1 in ESC. The concentration of endothelin-1 in cystic fluid of endometrioma or non-endometrioma was measured with ELISA. The conditioned medium of ESC stimulated with IL-1β and/or BK was injected intraplantarly in mice, and evaluated whether pain-related licking behaviour was elicited. RESULTS: The expressions of BK and BKR in endometriotic lesions were observed by immunohistochemistry. In vitro experiments showed that IL-1β induced BKR-B1 and B2 on ESC. Activation of these receptors by BK significantly induced endothelin-1 expression in ESC, which was negated completely by HOE-140, a BKR-B2 antagonist. The cystic fluid of endometrioma contained higher amount of endothelin-1 compared to non-endometrioma. Intraplantar injection of the conditioned medium of ESC treated with IL-1β and BK significantly induced licking behaviour, which was suppressed with BQ-123, an endothelin type-A receptor antagonist. CONCLUSIONS: The present study demonstrated the presence and the function of the BK axis in endometriosis, and established a potential new therapy target for endometriosis-related pain. SIGNIFICANCE: The present study demonstrated (1) the presence and the function of the BK system in endometriosis, (2) activation of BKR induced endothelin-1 in endometriotic lesion and (3) blocking endothelin-1 was effective to decrease pain.

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Condition tags

endometriosisendometrioma

MeSH descriptors

Bradykinin Endometriosis Endothelin-1 Pain Receptors, Bradykinin Stromal Cells Animals Animals Behavior, Animal Behavior, Animal Behavior, Animal Bradykinin Bradykinin Bradykinin Bradykinin Bradykinin B2 Receptor Antagonists Bradykinin B2 Receptor Antagonists Bradykinin B2 Receptor Antagonists Case-Control Studies Case-Control Studies

Citation neighborhood (2-hop)

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

References (34)

Cited by (14)

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