Hyeon Du Jang’s research while affiliated with Kangwon National University and other places

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Publications (1)


Thin Layer Chromatography. (A) UV 254 nm, (B) 10% H2SO4, (C) ρ-Anisaldehyde H2SO4, (D) FeCl3. The eluent system used was chloroform/methanol/water = 70:30:4 (v/v/v). ① oregonin standard, ② hirsutanonol standard, ③ hirsutenone standard, ④ Alnus japonica 50% EtOH extract, ⑤ Alnus japonica hot water extract (AJHW).
(A) Calibration curve and equation for hirsutanonol and hirsutenone, hirsutanonol: Y = 13,167X − 385.69 (R² = 0.9999), hirsutenone: Y = 15,625X + 2161.2 (R² = 0.9999); (B) HPLC chromatogram of hirsutanonol and hirsutenone; (C) HPLC chromatogram of Alnus japonica 50% EtOH extract at 1000 μg/mL; (D) HPLC chromatogram of AJHW at 1000 μg/mL.
Negative mode LC-MS/MS of AJHW: (A) extracted ion chromatogram of AJHW, (B) total ion chromatogram, where the highlighted section corresponds to the mass value of hirsutanonol, and (C) total ion chromatogram, where the highlighted section corresponds to the mass value of hirsutenone.
Effects of AJHW administration on exercise capacity and grip strength in mice with dexamethasone-induced muscle atrophy. (A) Endurance time to exhaustion, (B) exercise capacity, and (C) grip strength. All mice had an initial age of 8 weeks. G2–G6 were treated daily with dexamethasone (5 mg/kg) for 2 weeks. AJHW was administered daily for 4 weeks at 20 mg/kg (G3), 50 mg/kg (G4), 100 mg/kg (G5), and 200 mg/kg (G6). A total of ten animals was utilized in each group. Data are expressed as the mean ± SEM. *** p < 0.001 is significantly different from that of the G1 group. (G2). # p < 0.05, ## p < 0.01, are significantly different from that of G2 group. (G3, G4, G5, G6).
Effects of AJHW administration on fat and lean body percentage in mice with dexamethasone-induced muscle atrophy. (A) Fat percentage, (B) lean body percentage. All mice had an initial age of 8 weeks. G2–G6 were treated daily with dexamethasone (5 mg/kg) for 2 weeks. AJHW was administered daily for 4 weeks at 20 mg/kg (G3), 50 mg/kg (G4), 100 mg/kg (G5), and 200 mg/kg (G6). A total of ten animals was utilized in each group. Values are expressed as the mean ± SEM. ** p < 0.01 is significantly different from that of the G1 group. (G2). # p < 0.05, ## p < 0.01 are significantly different from that of G2 group. (G3, G4, G5, G6).

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Effects of Alnus japonica Pilot Scale Hot Water Extracts on a Model of Dexamethasone-Induced Muscle Loss and Muscle Atrophy in C57BL/6 Mice
  • Article
  • Full-text available

April 2025

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9 Reads

Hyeon Du Jang

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Chan Ho Lee

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Ye Eun Kwon

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[...]

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Sun Eun Choi

This study investigates the effects of pilot scale Alnus japonica hot water extract (AJHW) on muscle loss and muscle atrophy. Building on previous in vitro studies, in vivo experiments were conducted to evaluate muscle strength, mass, fiber size, protein synthesis, and antioxidant activity. The results showed that AJHW significantly restored muscle strength, increased muscle mass, enhanced the expression of muscle synthesis markers, such as Akt and mTOR, and apoptosis inhibition markers, such as Bcl-2, compared to the muscle atrophy control. Muscle degradation markers, such as Atrogin1, MuRF1, FoxO3α, and the apoptosis activation marker Bax, were decreased compared to the muscle atrophy control. Additionally, AJHW significantly boosted the activity of antioxidant factors like SOD, catalase, and Gpx, suggesting its protective role against oxidative stress-induced muscle damage. The enhanced effects were attributed to the high content of hirsutanonol and hirsutenone, which synergized with oregonin, compounds, identified through phytochemical analysis. While these findings support the potential of AJHW as a candidate for preventing muscle loss, further studies are needed to confirm its efficacy across diverse atrophy models and to elucidate its exact mechanisms.

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