Pengaruh Pemberian Leuprolide Acetat Terhadap Kadar IL-17A pada Mencit Model Endometriosis

In: Jurnal Surya Medika · 2024 · vol. 10(3) , pp. 105–108 · doi:10.33084/jsm.v10i3.8972 · W4406166730
article OA: diamond CC0
AI-generated summary by claude@2026-06, 2026-06-13

This study investigated the effect of Leuprolide Acetate administration on IL-17A levels in a mouse model of endometriosis, finding that it influenced these levels.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by claude@2026-06, 2026-06-13 · read from full text

This study examined how administering leuprolide acetate affects IL-17A levels in a mouse model of endometriosis. Fifteen mice were divided into three groups—healthy controls, untreated endometriosis model mice, and endometriosis model mice treated with leuprolide acetate—and IL-17A was measured using ELISA. The authors report that leuprolide acetate had an effect on IL-17A levels in the endometriosis model mice. The paper does not explicitly describe additional limitations beyond the brief methods and abstract-level findings, and it does not provide details on magnitude of change or experimental parameters in the provided text. This paper is centrally about endometriosis — it specifically tests the effect of leuprolide acetate on IL-17A levels in endometriosis model mice.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

Endometriosis adalah kelainan umum yang dikaitkan dengan nyeri, gejala gastrointestinal dan saluran kemih, infertilitas, dan kelelahan. Endometriosis didefinisikan oleh adanya lesi mirip endometrium yang sebagian besar ditemukan di panggul. Mekanisme yang berkontribusi terhadap etiologi penyakit ini meliputi perubahan jalur hormonal, inflamasi, dan nyeri IL-17A. Leuprolide Acetat adalah analog sintetik dari hormon pelepas gonadotropin (GnRH) yang terjadi secara alami, yang bertindak sebagai penghambat kuat sekresi gonadotropin hipofisis bila diberikan terus menerus pada dosis terapeutik. Penelitian ini bertujuan untuk melihat pengaruh pemberian Leuprolide Acetat terhadap Kadar IL-17A pada mencit model endometriosis. Sebanyak 15 ekor mencit di bagi menjadi 3 kelompok yaitu mencit sehat, mencit Endometriosis, mencit Endometriosis diberikan Leuprolide Acetat. Kadar IL-17A diukur dengan enzyme-linked immunosorbent assay (ELISA) pada masing-masing kelompok pengamatan. Dari hasil penelitian ini menunjukkan bahwa terdapat pengaruh pemberian Leuprolide Acetat terhadap kadar IL-17A pada mencit model endometriosis.
Full text 4,686 characters · extracted from oa-doi-fallback · 2 sections · click to expand

Abstract

Endometriosis adalah kelainan umum yang dikaitkan dengan nyeri, gejala gastrointestinal dan saluran kemih, infertilitas, dan kelelahan. Endometriosis didefinisikan oleh adanya lesi mirip endometrium yang sebagian besar ditemukan di panggul. Mekanisme yang berkontribusi terhadap etiologi penyakit ini meliputi perubahan jalur hormonal, inflamasi, dan nyeri IL-17A. Leuprolide Acetat adalah analog sintetik dari hormon pelepas gonadotropin (GnRH) yang terjadi secara alami, yang bertindak sebagai penghambat kuat sekresi gonadotropin hipofisis bila diberikan terus menerus pada dosis terapeutik. Penelitian ini bertujuan untuk melihat pengaruh pemberian Leuprolide Acetat terhadap Kadar IL-17A pada mencit model endometriosis. Sebanyak 15 ekor mencit di bagi menjadi 3 kelompok yaitu mencit sehat, mencit Endometriosis, mencit Endometriosis diberikan Leuprolide Acetat. Kadar IL-17A diukur dengan enzyme-linked immunosorbent assay (ELISA) pada masing-masing kelompok pengamatan. Dari hasil penelitian ini menunjukkan bahwa terdapat pengaruh pemberian Leuprolide Acetat terhadap kadar IL-17A pada mencit model endometriosis. Downloads Article Details This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License. All rights reserved. This publication may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying, recording.

References

Ahn, S. H., Edwards, A. K., Singh, S. S., Young, S. L., Lessey, B. A., & Tayade, C. 2015. IL-17A Contributes to the Pathogenesis of Endometriosis by Triggering Proinflammatory Cytokines and Angiogenic Growth Factors. Journal of Immunology (Baltimore, Md. : 1950), 195(6), 2591–2600. https://doi.org/10.4049/jimmunol.1501138 Barnard, N. D., Holtz, D. N., Schmidt, N., Kolipaka, S., Hata, E., Sutton, M., Znayenko-Miller, T., Hazen, N. D., Cobb, C., & Kahleova, H. 2023. Nutrition in the prevention and treatment of endometriosis: A review. Frontiers in Nutrition, 10. https://www.frontiersin.org/journals/nutrition/articles/10.3389/fnut.2023.1089891 Griffiths, M. J., Horne, A. W., Gibson, D. A., Roberts, N., & Saunders, P. T. K. 2024. Endometriosis: recent advances that could accelerate diagnosis and improve care. Trends in Molecular Medicine, 30(9), 875–889. https://doi.org/10.1016/j.molmed.2024.06.008 Harada, T., Osuga, Y., Suzuki, Y., Fujisawa, M., Fukui, M., & Kitawaki, J. 2022. Relugolix, an oral gonadotropin-releasing hormone receptor antagonist, reduces endometriosis-associated pain compared with leuprorelin in Japanese women: a phase 3, randomized, double-blind, noninferiority study. Fertility and Sterility, 117(3), 583–592. https://doi.org/10.1016/j.fertnstert.2021.11.013 Horne, A. W., & Missmer, S. A. 2022. Pathophysiology, diagnosis, and management of endometriosis. BMJ (Clinical Research Ed.), 379, e070750. https://doi.org/10.1136/bmj-2022-070750 Hoseininasab, F., Mehrjardi, Y. V., Javaheri, A., Tajamolian, M., & Samadi, M. 2024. Study on gene expression of IL-17A in eutopic and ectopic tissue sample of endometriosis patients and comparison with control group. Biomedical Research and Therapy, 11(6), 6482–6487. Krina T. Zondervan, D.Phil., Christian M. Becker, M. D., & and Stacey A. Missmer, S. D. 2020. Endometriosis, Review Article. N Engl J Med, 382(1244), 56. https://doi.org/10.1056/NEJMra1810764 Magon, N. 2011. Gonadotropin releasing hormone agonists: Expanding vistas. Indian Journal of Endocrinology and Metabolism, 15(4), 261–267. https://doi.org/10.4103/2230-8210.85575 Prentice, A., Aj, D., Farquhar, C., & Sk, S. 2011. Gonadotrophin-releasing hormone analogues for pain associated with endometriosis: Commentary. Obstetrics and Gynecology, 117(3), 727–728. https://doi.org/10.1097/AOG.0b013e31820cb0fd Shi, J. L., Zheng, Z. M., Chen, M., Shen, H. H., Li, M. Q., & Shao, J. 2022. IL-17: an important pathogenic factor in endometriosis. International Journal of Medical Sciences, 19(4), 769–778. https://doi.org/10.7150/ijms.71972 Sutrisno, S., Miryani, I., Dwijayasa, P. M., Suprobo, N. R., & Wiyasa, I. W. A. 2022. Genistein administration increases the level of superoxide dismutase and glutathione peroxidase in the endometriosis mice model: An experimental study. International Journal of Reproductive BioMedicine, 20(10), 873–882. https://doi.org/10.18502/ijrm.v20i10.12271 Zhou, W., Yang, H., Shao, J., Mei, J., Chang, K., Zhu, R., & Li, M. 2019. sitokin anti inflamasi pada endometriosis. 0123456789

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Condition tags

endometriosis

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2024) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

Source provenance

openalex
last seen: 2026-06-10T17:14:06.276822+00:00
License: CC0 · commercial use OK