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[1]鄭俊杰,陳冬冬,林佳生,等.褪黑素對(duì)骨質(zhì)疏松大鼠骨代謝及成骨細(xì)胞Wnt/β-catenin信號(hào)通路的影響[J].福建醫(yī)藥雜志,2023,45(04):111-114.
 ZHENG Junjie,CHEN Dongdong,LIN Jiasheng,et al.Effect of melatonin on bone metabolism and osteoblast Wnt/β-catenin signaling pathway in osteoporotic rats[J].FUJIAN MEDICAL JOURNAL,2023,45(04):111-114.
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褪黑素對(duì)骨質(zhì)疏松大鼠骨代謝及成骨細(xì)胞Wnt/β-catenin信號(hào)通路的影響()
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《福建醫(yī)藥雜志》[ISSN:1002-2600/CN:35-1071/R]

卷:
45
期數(shù):
2023年04期
頁(yè)碼:
111-114
欄目:
基礎(chǔ)研究
出版日期:
2023-08-15

文章信息/Info

Title:
Effect of melatonin on bone metabolism and osteoblast Wnt/β-catenin signaling pathway in osteoporotic rats
文章編號(hào):
1002-2600(2023)04-0111-04
作者:
鄭俊杰陳冬冬林佳生嚴(yán)偉洪嘉祥宋平陳嶸1
福建省福州市第二醫(yī)院骨與軟組織腫瘤科(福州 350007)
Author(s):
ZHENG Junjie CHEN Dongdong LIN Jiasheng YAN Wei HONG Jiaxiang SONG Ping CHEN Rong
Department of Bone and Soft Tissue Oncology, Fuzhou Second Hospital, Fuzhou, Fujian 350007, China
關(guān)鍵詞:
褪黑素 骨質(zhì)疏松 骨代謝 Wnt/β-catenin
Keywords:
melatonin osteoporosis bone metabolism Wnt/β-catenin
分類號(hào):
R58
文獻(xiàn)標(biāo)志碼:
B
摘要:
目的 探討褪黑素對(duì)骨質(zhì)疏松大鼠骨代謝及成骨細(xì)胞Wnt/β-catenin信號(hào)通路的影響。方法 按照隨機(jī)數(shù)字表法將60只大鼠分成空白組、模型組和褪黑素組。空白組使用與褪黑素同等劑量的生理鹽水進(jìn)行灌胃; 模型組在空白組的基礎(chǔ)上行雙側(cè)卵巢切除術(shù),構(gòu)建骨質(zhì)疏松大鼠模型; 褪黑素組在模型組的基礎(chǔ)上,采用靜脈注射的方式給予褪黑素治療。采用ELISA法檢測(cè)3組大鼠血清中堿性磷酸酶(ALP)、Ⅰ型前膠原氨基端原肽(PINP)、骨鈣素(OC)、I型膠原C端交聯(lián)肽(CTX-Ⅰ)的含量。采用RT-PCR及Western blot法檢測(cè)大鼠成骨細(xì)胞中Wnt/β-catenin信號(hào)通路相關(guān)因子細(xì)胞β-連環(huán)蛋白(β-catenin)、無(wú)翅型MMTV整合位點(diǎn)家族成員3A(Wnt3a)、無(wú)翅型MMTV整合位點(diǎn)家族成員7B(Wnt7b)、軸抑制蛋白2抗體(Axin2)的mRNA及蛋白表達(dá)。結(jié)果 與模型組比較,褪黑素組大鼠血清中的ALP、PINP、OC、CTX-Ⅰ含量得到提升,差異有統(tǒng)計(jì)學(xué)意義(P<0.05)。與模型組比較,褪黑素組大鼠成骨細(xì)胞的β-catenin、Wnt7b的mRNA和蛋白含量明顯升高(P<0.05),Axin2的mRNA和蛋白含量明顯降低(P<0.05)。結(jié)論 褪黑素能夠調(diào)節(jié)骨代謝平衡,并通過(guò)激活Wnt/β-catenin信號(hào)通路促進(jìn)成骨細(xì)胞的形成。
Abstract:
Objective To investigate the effect of melatonin on bone metabolism and osteoblast Wnt /β-catenin signaling pathway in osteoporotic rats. Methods According to the random number table method,60 rats were divided into blank group,model group and melatonin group. The blank group was intragastrically administered with the same dose of normal saline as melatonin; the model group underwent bilateral ovariectomy on the basis of the blank group to construct a rat model of osteoporosis; on the basis of the model group, the melatonin group was treated with melatonin by intravenous injection. The contents of alkaline phosphatase(ALP), type I procollagen amino terminal propeptide(PINP), osteocalcin(OC)and type I collagen C-terminal cross-linked peptide(CTX-I)in serum of rats in the three groups were detected by ELISA. The mRNA and protein expression of Wnt/β-catenin signaling pathway related factors β-catenin,Wnt3a,Wnt7b and Axin2 in rat osteoblasts were detected by RT-PCR and Western blot. Results Compared with the model group,the contents of ALP,PINP,OC and CTX-I in the serum of the melatonin group were increased significantly(P<0.05). Compared with the model group,the mRNA and protein levels of β-catenin and Wnt7b in osteoblasts of rats in the melatonin group were significantly increased(P<0.05),and the mRNA and protein levels of Axin2 were significantly decreased(P<0.05). Conclusion Melatonin can regulate the balance of bone metabolism and promote the formation of osteoblasts by activating the Wnt/β-catenin signaling pathway.

參考文獻(xiàn)/References:

[1] Compston J E,McClung M R,Leslie W D.Osteoporosis[J].Lancet,2019,393(10169):364-376.
[2] Levin V A,Jiang X,Kagan R.Estrogen therapy for osteoporosis in the modern era[J].Osteoporos Int,2018,29(5):1049-1055.
[3] Hardeland R.Aging,melatonin,and the pro-and anti-inflammatory networks[J].Int J Mol Sci,2019,20(5):1223.
[4] Liu W,Yu M,XIE D,et al.Melatonin-stimulated MSC-derived exosomes improve diabetic wound healing through regulating macrophage M1 and M2 polarization by targeting the PTEN/AKT pathway[J].Stem Cell Res Ther,2020,11(1):259.
[5] Thompson D D,Simmons H A,Pirie C M,et al.FDA Guidelines and animal models for osteoporosis[J].Bone,1995; 17(S4):125-133.
[6] Ott S M.Osteoporosis drugs may improve BMD and reduce fractures in some patients with CKD[J].Annals of Internal Medicine,2017,167(4):JC19.
[7] 王旭東,黃東生.褪黑素防治骨質(zhì)疏松癥的研究現(xiàn)狀[J].中國(guó)骨質(zhì)疏松雜志,2020,26(5):741-745.
[8] Reiter R,Tan D,Rosales-Corral S,et al.Melatonin mitigates mitochondrial meltdown:Interactions with SIRT3[J].International Journal of Molecular Sciences,2018,19(8):2439.
[9] Sharan K,Lewis K,Furukawa T,et al.Regulation of bone mass throughpineal-derived melatonin-MT2 receptor pathway [J].J Pineal Res,2017,63(2):1-12.
[10] Ping Z C,Hu X Y,Wang L L,et al.Melatonin attenuates titanium particle-induced osteolysis via activation of Wnt/β-catenin signaling pathway [J].Acta Biomaterialia,2017(51):513-525.
[11] 馮宜蒀,來(lái)積芳,宋敏,等.固本增骨方聯(lián)合高壓氧療對(duì)骨質(zhì)疏松癥模型大鼠骨代謝平衡的影響[J].中醫(yī)雜志,2021,62(5):433-438.
[12] 邵榮學(xué),張亮,楊賀杰,等.泛素-蛋白酶體抑制劑MG132上調(diào)Wnt/β-catenin信號(hào)通路改善骨質(zhì)疏松的實(shí)驗(yàn)研究[J].中國(guó)骨傷,2022,35(1):59-64.

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備注/Memo

備注/Memo:
基金項(xiàng)目:福建省科技創(chuàng)新平臺(tái)項(xiàng)目“2020年福建省創(chuàng)傷骨科急救與康復(fù)臨床醫(yī)學(xué)研究中心”(2020Y2014)
1 通信作者,Email:[email protected]
更新日期/Last Update: 2023-08-15