RANKL-derived peptide MHP1-AcN attenuates ovariectomy-induced osteoporosis by targeting RANK and TNFR1 in mice

MHP1-AcN effectively inhibits osteoclastogenesis and sclerostin-mediated suppression of bone formation while considerably preserving osteoblast function. These findings suggest that MHP1-AcN, which targets dual pathways critical for bone homeostasis, is a promising uncoupling therapeutic agent for osteoporosis.

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Publication Details

Journal
Bone
Published
2025-03-01
DOI
https://doi.org/10.1016/j.bone.2025.117440
Citations
7
Primary Topic
Bone Metabolism and Diseases
Type
article
Field-Weighted Citation Impact
5.64
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RANKL-derived peptide MHP1-AcN attenuates ovariectomy-induced osteoporosis by targeting RANK and TNFR1 in mice

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article

RANKL-derived peptide MHP1-AcN attenuates ovariectomy-induced osteoporosis by targeting RANK and TNFR1 in mice

Nagahiro Ochiai, Atsushi Sugimoto, Yuji Fukuda, Yuki Etani, Takaaki Noguchi, Taihei Miura, Ken Nakata, Kosuke Ebina, Munehisa Shimamura, Makoto Hirao, Seiji Okada, Atsushi Goshima, Nan Ju, Takashi Kanamoto, Satoshi Yamakawa, Takuya Kurihara
article en
7 citations

Abstract

MHP1-AcN effectively inhibits osteoclastogenesis and sclerostin-mediated suppression of bone formation while considerably preserving osteoblast function. These findings suggest that MHP1-AcN, which targets dual pathways critical for bone homeostasis, is a promising uncoupling therapeutic agent for osteoporosis.

BoneVol. 194
Kisarazu Hospital (JP), Osaka Rosai Hospital (JP), Osaka Minami Medical Center (JP), The University of Osaka (JP)
Zero hunger
Openalex Percentile: Top 4%
Bone Metabolism and Diseases
5.64
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