Tian-shuang XIA, Liu-yue LIN, Qiao-yan ZHANG, 等. Humulus lupulus L. Extract Prevents Ovariectomy-Induced Osteoporosis in Mice and Regulates Activities of Osteoblasts and Osteoclasts[J]. Chinese Journal of Integrative Medicine, 2021,27(1):31-38.
Tian-shuang XIA, Liu-yue LIN, Qiao-yan ZHANG, et al. Humulus lupulus L. Extract Prevents Ovariectomy-Induced Osteoporosis in Mice and Regulates Activities of Osteoblasts and Osteoclasts[J]. Chinese Journal of Integrative Medicine, 2021,27(1):31-38.
Tian-shuang XIA, Liu-yue LIN, Qiao-yan ZHANG, 等. Humulus lupulus L. Extract Prevents Ovariectomy-Induced Osteoporosis in Mice and Regulates Activities of Osteoblasts and Osteoclasts[J]. Chinese Journal of Integrative Medicine, 2021,27(1):31-38. DOI: 10.1007/s11655-019-2700-z.
Tian-shuang XIA, Liu-yue LIN, Qiao-yan ZHANG, et al. Humulus lupulus L. Extract Prevents Ovariectomy-Induced Osteoporosis in Mice and Regulates Activities of Osteoblasts and Osteoclasts[J]. Chinese Journal of Integrative Medicine, 2021,27(1):31-38. DOI: 10.1007/s11655-019-2700-z.
Humulus lupulus L. Extract Prevents Ovariectomy-Induced Osteoporosis in Mice and Regulates Activities of Osteoblasts and Osteoclasts
摘要
Abstract
Objective:
2
To systematically evaluate the protective effects of
Humulus lupulus
L. extract (HLE) on osteoporosis mice.
Methods:
2
In vivo
experiment
a total of 35 12-week-old female ICR mice were equally divided into 5 groups: the sham control group (sham); the ovariectomy with vehicle group (OVX); the OVX with estradiol valerate [EV
0.2 mg/(kg•d)]; the OVX with low- or high-dose HLE groups [HLE
1 g/(kg•d) and 3 g/(kg•d)]
7 in each group. Treatment began 1 week after the ovariectomized surgery and lasted for 12 weeks. Bone mass and trabecular bone mircoarchitecture were evaluated by micro computed tomography
and bone turnover markers in serum were evaluated using enzyme-linked immunosorbent assay (ELISA) kits.
In vitro
experiment
osteoblasts and osteoclasts were treated with HLE at doses of 0
4
20 and 100 μg/mL. Biomarkers for bone formation in osteoblasts and bone resorption in osteoclasts were analyzed.
Results:
2
Compared with the OVX group
HLE exerted bone protective effects by the increase of estradiol (
P
<
0.05)
the improvement of cancellous bone structure
bone mineral density (
P
<
0.01) and the reduction of serum alkaline phosphatase (ALP)
tartrate resistant acid phosphatase (TRAP)
bone gla-protein
c-terminal telopeptides of type Ⅰ collagen (CTX-Ⅰ) and deoxypyridinoline levels (
P
<
0.01 for all).
In vitro
experiment
compared with the control group
HLE at 20 μg/mL promoted the cell proliferation (
P
<
0.01)
and increased the expression of bone morphogenetic protein-2 and osteopontin levels in osteoblasts (both
P
<
0.05). HLE at 100 μg/mL increased the osteoblastic ALP activities
and HLE at all dose enhanced the extracellular matrix mineralization (both
P
<
0.01). Furthermore
compared with the control group
HLE at 20 μg/mL and 100 μg/mL inhibited osteoclastic TRAP activity (
P
<
0.01)
and reduced the expression of matrix metalloproteinase-9 and cathepsin K (both
P
<
0.05).
Conclusion:
2
HLE may protect against bone loss
and have potentials in the treatment of osteoporosis.
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相关机构
Department of Pharmacy, Sun Yat-sen Memorial Hospital, Sun Yat-sen University
Good Clinical Practice Development, Guangdong Provincial Key Laboratory of Bone and Joint Degeneration Diseases, The Third Affiliated Hospital of Southern Medical University
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Taif University
Basic Medical Sciences Department, College of Medicine at King Saud bin Abdulaziz University for Health Sciences (KSAU-)
Medical Physiology Department, Faculty of Medicine, Mansoura, University