# The Effects of a Novel Astragalus-Based Extract (Keyfobell Powder (KFB)) on Longitudinal Bone Growth via IGF-1 Upregulation: A Potential Growth Hormone Alternative

**Authors:** Myong Jin Lee, Daesik Jeong, Ji Hwan Lee, Jaeha Kang, Jihye Choi, Jaeok Seo, Hong Il Kim, Jisoo Seo, Kiseong Ko, Dong Hyuk Nam, Hye Lim Lee, Ki Sung Kang

PMC · DOI: 10.3390/nu17030416 · Nutrients · 2025-01-23

## TL;DR

This study explores a new Astragalus-based extract that may promote bone growth by boosting IGF-1, potentially serving as a natural alternative to growth hormone.

## Contribution

A novel Astragalus-based extract is proposed as a growth hormone alternative by upregulating IGF-1 for longitudinal bone growth.

## Key findings

- KFB increased body weight and bone growth in a dose-dependent manner in rats.
- KFB elevated IGF-1 and IGFBP-3 levels similarly to growth hormone treatment.
- Network analysis suggests KFB compounds may regulate key growth-related signaling pathways.

## Abstract

Background/Objectives: This study evaluated the effects of a novel Astragalus extract (Keyfobell powder [KFB]) composed of Astragalus membranaceus, red ginseng (Panax ginseng C. A. Meyer), and Cervi Parvum Cornu as a potential growth hormone (GH) alternative. The primary focus was placed on its impact on longitudinal bone growth through the upregulation of circulatory insulin-like growth factor (IGF)-1. Methods: We performed in vitro and in vivo experiments using a hypothalamic cell line and Sprague–Dawley (SD) rats. Quantitative RT-PCR was performed to determine growth hormone-releasing hormone (GHRH) and ghrelin mRNA expressions in GT1-7 cells. The treatment groups were administered KFB at various dosages, and the positive controls received recombinant human GH. Body weight, bone length, and density were assessed, along with serum levels of insulin-like growth factor binding protein (IGFBP)-3 and IGF-1. Results: KFB and somatropin exhibited no cytotoxic effect in GT1-7 cells and increased GHRH and ghrelin mRNA levels in a dose-dependent manner. KFB administration resulted in a significant dose-dependent increase in body weight and bone growth (femur and tibia). Changes in IGF-1 and IGFBP-3 levels were comparable to those observed in the GH-treated group. Based on network pharmacological analysis, multiple compounds in KFB ((20S)-20-hydroxypregn-4-en-3-one, 2-isopropyl-3-methoxypyrazine, caproic acid, daidzein, furfuryl alcohol, lauric acid, octanal, and salicylic acid) may synergistically regulate the PI3K-Akt, Ras, and Rap1 signaling pathways linked to growth control and cartilage formation, leading to a possible increase in height. Conclusions: Our results suggest that KFB can function as a GH-mimetic agent that promotes bone growth through IGF-1 upregulation.

## Linked entities

- **Proteins:** IGF1 (insulin like growth factor 1), IGFBP3 (insulin like growth factor binding protein 3), GHRH (growth hormone releasing hormone), GHRL (ghrelin and obestatin prepropeptide)
- **Chemicals:** (20S)-20-hydroxypregn-4-en-3-one (PubChem CID 8956), 2-isopropyl-3-methoxypyrazine (PubChem CID 33166), caproic acid (PubChem CID 8892), daidzein (PubChem CID 5281708), furfuryl alcohol (PubChem CID 7361), lauric acid (PubChem CID 3893), octanal (PubChem CID 454), salicylic acid (PubChem CID 338)
- **Species:** Astragalus membranaceus (taxon 649199)

## Full-text entities

- **Genes:** Akt1 (Akt serine/threonine kinase 1) [NCBI Gene 11651] {aka Akt, LTR-akt, PKB, PKB/Akt, PKBalpha, Rac}, Ghrl (ghrelin) [NCBI Gene 58991] {aka 2210006E23Rik, Ghr, MTLRP, MTLRPAP, m46}, Igfbp3 (insulin-like growth factor binding protein 3) [NCBI Gene 16009] {aka IGFBP-3, IGgfbp3}, Rap1a (Rap1a member of RAS oncogene family) [NCBI Gene 109905] {aka G-22K, Krev-1, Rap1}, Igf1 (insulin-like growth factor 1) [NCBI Gene 16000] {aka C730016P09Rik, Igf-1, Igf-I}, Ghrh (growth hormone releasing hormone) [NCBI Gene 14601] {aka GRF, Ghrf}, GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}
- **Diseases:** cytotoxic (MESH:D064420)
- **Chemicals:** daidzein (MESH:C004742), (20S)-20-hydroxypregn-4-en-3-one (-), somatropin (MESH:D019382), octanal (MESH:C031639), caproic acid (MESH:C037652), salicylic acid (MESH:D020156), lauric acid (MESH:C030358), 2-isopropyl-3-methoxypyrazine (MESH:C024267), furfuryl alcohol (MESH:C012986)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Astragalus membranaceus (species) [taxon 649199]
- **Cell lines:** GT1-7 — Mus musculus (Mouse), Transformed cell line (CVCL_0281)

## Full text

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## Figures

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## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC11820268/full.md

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Source: https://tomesphere.com/paper/PMC11820268