# Anti-Obesity Effects of a Standardized Prunus persica Flower Extract (HT099) Through the Regulation of Lipid Metabolism in High-Fat Diet-Induced Obese Mice

**Authors:** Se-Young Kim, Minju Kim, Young-Woong Choi, Mi-Yeon Kim, Kun Yun, Young-Sik Kim, Hocheol Kim

PMC · DOI: 10.3390/metabo16020132 · 2026-02-13

## TL;DR

This study shows that a peach blossom extract called HT099 helps reduce obesity and improve metabolism in mice fed a high-fat diet.

## Contribution

The novel contribution is the identification of HT099 as a natural compound with anti-obesity effects through regulation of lipid metabolism and gene expression.

## Key findings

- HT099 reduced body weight gain and white adipose tissue accumulation in obese mice.
- The extract improved glucose tolerance and serum lipid profiles, including lower triglycerides and higher HDL cholesterol.
- HT099 modulated gene expression related to lipid metabolism, increasing AMPKα1 and decreasing adipogenic and lipogenic genes.

## Abstract

Background: Obesity is one of the most prevalent metabolic disorders worldwide, and its long-term management remains challenging due to the limited efficacy and adverse effects of current pharmacological treatments. Accordingly, there is growing interest in safe and effective anti-obesity strategies based on natural compounds. This study aimed to evaluate the anti-obesity effects of HT099, an extract derived from Prunus persica (peach blossom), and to investigate molecular changes associated with its metabolic effects in a high-fat diet (HFD)-induced obesity mouse model. Methods: Male C57BL/6N mice were fed an HFD and orally administered HT099 (50 or 100 mg/kg) or the positive control orlistat (40 mg/kg) for 12 weeks. Body weight, adipose tissue accumulation, food efficiency ratio, glucose tolerance, serum lipid profiles, and hepatic gene expression related to lipid metabolism were evaluated. Results: HT099 supplementation significantly attenuated body weight gain and reduced white adipose tissue accumulation while improving food efficiency ratio. HT099 also ameliorated HFD-induced glucose intolerance and favorably modulated serum lipid profiles, including reduced triglyceride levels, increased HDL-cholesterol levels, and improved non-HDL cholesterol indices. At the molecular level, HT099 administration was associated with an increased hepatic AMPKα1 mRNA expression and decreased expression of adipogenic and lipogenic genes, including C/EBPα, PPARγ, FAS, and SREBP-1c. Conclusions: These findings indicate that HT099 exerts anti-obesity effects in HFD-induced obese mice, accompanied by improvements in lipid and glucose metabolism and changes in adipogenesis- and lipogenesis-related gene expression. Collectively, the results support the potential of HT099 as a natural bioactive agent for obesity management.

## Linked entities

- **Genes:** PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562], CEBPA (CCAAT enhancer binding protein alpha) [NCBI Gene 1050], PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468], FAS (Fas cell surface death receptor) [NCBI Gene 355], Srebf1 (sterol regulatory element binding transcription factor 1) [NCBI Gene 78968]
- **Diseases:** obesity (MONDO:0011122)

## Full-text entities

- **Genes:** Ppara (peroxisome proliferator activated receptor alpha) [NCBI Gene 19013] {aka 4933429D07Rik, Nr1c1, PPAR-alpha, PPARalpha, Ppar}, Cebpa (CCAAT/enhancer binding protein alpha) [NCBI Gene 12606] {aka C/ebpalpha, CBF-A, Cebp}, Srebf1 (sterol regulatory element binding transcription factor 1) [NCBI Gene 20787] {aka ADD1, SREBP1, bHLHd1}, Ucp1 (uncoupling protein 1 (mitochondrial, proton carrier)) [NCBI Gene 22227] {aka Slc25a7, Ucp}, Lep (leptin) [NCBI Gene 16846] {aka ob, obese}, Ppargc1a (peroxisome proliferative activated receptor, gamma, coactivator 1 alpha) [NCBI Gene 19017] {aka A830037N07Rik, Gm11133, PGC-1, PPARGC-1-alpha, Pgc-1alpha, Pgc1}, Adipoq (adiponectin, C1Q and collagen domain containing) [NCBI Gene 11450] {aka 30kDa, APN, Acdc, Acrp30, Ad, Adid}, Prkaa1 (protein kinase, AMP-activated, alpha 1 catalytic subunit) [NCBI Gene 105787] {aka AMPKalpha1, C130083N04Rik}, Pparg (peroxisome proliferator activated receptor gamma) [NCBI Gene 19016] {aka Nr1c3, PPAR-gamma, PPAR-gamma2, PPARgamma, PPARgamma2}
- **Diseases:** glucose intolerance (MESH:D018149), constipation (MESH:D003248), type 2 diabetes (MESH:D003924), abdominal adiposity (MESH:D000007), adiposity (MESH:D018205), weight (MESH:D015431), cardiovascular disease (MESH:D002318), metabolic disorders (MESH:D008659), OS (MESH:C567932), fat (MESH:D004620), overweight (MESH:D050177), weight gain (MESH:D015430), Obese (MESH:D009765), weight regain (MESH:D055191), edema (MESH:D004487), cardiovascular and central nervous system symptoms (MESH:D002493), dyslipidemia (MESH:D050171), injury to (MESH:D014947), Disease (MESH:D004194), metabolic disturbances (MESH:D024821)
- **Chemicals:** flavonoid (MESH:D005419), Chlorogenic acid (MESH:D002726), Glucose (MESH:D005947), CAS (MESH:D002118), caffeic acid (MESH:C040048), Lipid (MESH:D008055), p-coumaric acid (MESH:C495469), naringenin (MESH:C005273), Sodium carbonate (MESH:C005686), OS (MESH:D009992), polyphenol (MESH:D059808), neochlorogenic acid (MESH:C473200), phosphoric acid (MESH:C030242), multiflorin A (MESH:C087918), Orlistat (MESH:D000077403), Al (MESH:D000535), Folin-Ciocalteu's phenol (-), cholesterol (MESH:D002784), Blood glucose (MESH:D001786), isoflurane (MESH:D007530), phenolic acids (MESH:C017616), ferulic acid (MESH:C004999), DW (MESH:D014867), phentermine (MESH:D010645), kaempferol (MESH:C006552), acetonitrile (MESH:C032159), TG (MESH:D014280), rutin (MESH:D012431), Gallic acid (MESH:D005707), Fat (MESH:D005223), saline (MESH:D012965), methanol (MESH:D000432)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Prunus persica (peach, species) [taxon 3760]
- **Mutations:** G7111A, G7129A, C150P, G7155A
- **Cell lines:** HT099 — Homo sapiens (Human), Induced pluripotent stem cell (CVCL_JT93), C57BL/6N — Mus musculus (Mouse), Embryonic stem cell (CVCL_2H81)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942175/full.md

---
Source: https://tomesphere.com/paper/PMC12942175