Du-Zhong (Eucommia ulmoides Oliv.) Cortex Extract Alleviates Lead Acetate-Induced Bone Loss in Rats

被引:0
|
作者
Shanshan Qi
Hongxing Zheng
Chen Chen
Hai Jiang
机构
[1] Shaanxi University of Technology,Vitamin D Research Institute
[2] Shaanxi University of Technology,College of Biological Science and Engineering
[3] Shaanxi University of Technology,Chinese
来源
关键词
Oliv; Lead; BMD; Bone histomorphology; Rats;
D O I
暂无
中图分类号
学科分类号
摘要
The purpose of this study was to evaluate the protective effect of Du-Zhong cortex extract (DZCE) on lead acetate-induced bone loss in rats. Forty female Sprague-Dawley rats were randomly divided into four groups: group I (control) was provided with distilled water. Group II (PbAc) received 500 ppm lead acetate in drinking water for 60 days. Group III (PbAc+DZCE) received 500 ppm lead acetate in drinking water, and given intragastric DZCE (100 mg/kg body weight) for 60 days. Group IV (DZCE) was given intragastric DZCE (100 mg/kg body weight) for 60 days. The bone mineral density, serum biochemical markers, bone histomorphology, and bone marrow adipocyte parameters were analyzed using dual-energy X-ray absorptiometry, biochemistry, histomorphometry, and histopathology, respectively. The results showed that the lumbar spine and femur bone mineral density was significantly decreased in PbAc group compared with the control (P < 0.05); however, this decrease was inhibited by the intake of Du-Zhong cortex extract (P < 0.05, vs. PbAc group; P > 0.05, vs. control and DZCE group). Serum calcium and serum phosphorus in the PbAc+DZCE group were greater than that in the PbAc group (P < 0.05). The PbAc group had higher ALP, osteocalcin, and RANKL than the control group (P < 0.01), and they were significantly lower in the PbAc+DZCE group compared with the PbAc group. There were no significant differences of ALP, osteocalcin, and RANKL among the PbAc+DZCE, control, and DZCE groups (P > 0.05). Serum OPG and OPG/RANKL ration were significantly higher in the PbAc+DZCE group than that in the PbAc group (P < 0.05). The bone histomorphometric analyses showed that bone volume and trabecular thickness in the femoral trabecular bone were significantly lower in the PbAc group than that in the control group, but those were restored in the PbAc+DZCE groups. The bone marrow adipocyte number, percent adipocyte volume per tissue volume (AV/TV), and mean adipocyte diameter were significantly increased in the PbAc group compared to the control (P < 0.01), and those were restored in the PbAc+DZCE group. The differences of those parameters between PbAc+DZCE, DZCE, and the control group were not significant. The results above indicate that the Du-Zhong cortex extract has protective effects on both stimulation of bone formation and suppression of bone resorption in lead-exposed rats, therefore, Du-Zhong cortex extract has the potential to prevent or treat osteoporosis resulting from lead expose.
引用
收藏
页码:172 / 180
页数:8
相关论文
共 43 条
  • [21] Mechanism of the Inhibitory Effects of Eucommia ulmoides Oliv. Cortex Extracts (EUCE) in the CCl4-Induced Acute Liver Lipid Accumulation in Rats
    Jin, Chang-Feng
    Li, Bo
    Lin, Shun-Mei
    Yadav, Raj-Kumar
    Kim, Hyung-Ryong
    Chae, Han-Jung
    INTERNATIONAL JOURNAL OF ENDOCRINOLOGY, 2013, 2013
  • [22] Endothelium-dependent vascular relaxation induced by Eucommia ulmoides Oliv. bark extract is mediated by NO and EDHF in small vessels
    Kwan, CY
    Zhang, WB
    Deyama, T
    Nishibe, S
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2004, 369 (02) : 206 - 211
  • [23] Endothelium-dependent vascular relaxation induced by Eucommia ulmoides Oliv. bark extract is mediated by NO and EDHF in small vessels
    Chiu-Yin Kwan
    Wen-Bo Zhang
    Takeshi Deyama
    Sansei Nishibe
    Naunyn-Schmiedeberg's Archives of Pharmacology, 2004, 369 : 206 - 211
  • [24] An alcohol extract prepared from the male flower of Eucommia ulmoides Oliv. promotes synoviocyte apoptosis and ameliorates bone destruction in rheumatoid arthritis
    Yan Zhang
    Jian-Ying Wang
    Hao Wang
    Xiao-Yun Chen
    Lei Zhang
    Ying Yuan
    Chinese Medicine, 16
  • [25] Ameliorative effect of Eucommia ulmoides Oliv. leaves extract (ELE) on insulin resistance and abnormal perivascular innervation in fructose-drinking rats
    Jin, Xin
    Amitani, Keisuke
    Zamami, Yoshito
    Takatori, Shingo
    Hobara, Narumi
    Kawamura, Naomi
    Hirata, Tetsuya
    Wada, Atsunori
    Kitamura, Yoshihisa
    Kawasaki, Hiromu
    JOURNAL OF ETHNOPHARMACOLOGY, 2010, 128 (03) : 672 - 678
  • [26] An alcohol extract prepared from the male flower of Eucommia ulmoides Oliv. promotes synoviocyte apoptosis and ameliorates bone destruction in rheumatoid arthritis
    Zhang, Yan
    Wang, Jian-Ying
    Wang, Hao
    Chen, Xiao-Yun
    Zhang, Lei
    Yuan, Ying
    CHINESE MEDICINE, 2021, 16 (01)
  • [27] Hypoglycemic and hypolipidemic action of Du-zhong (Eucommia ulmoides Oliver) leaves water extract in C57BL/KsJ-db/db mice
    Park, Sun Ae
    Choi, Myung-Sook
    Kim, Myung-Joo
    Jung, Un Ju
    Kim, Hye-Jin
    Park, Kwan-Kyu
    Noh, Hey Jeong
    Park, Hae-Mo
    Park, Yong Bok
    Lee, Jeong-Sook
    Lee, Mi-Kyung
    JOURNAL OF ETHNOPHARMACOLOGY, 2006, 107 (03) : 412 - 417
  • [28] Polysaccharides from Eucommia ulmoides Oliv. leaves alleviates alcohol-induced mouse brain injury and BV-2 microglial dysfunction
    Li, Yingzhi
    Wang, Luchen
    Wang, Huimei
    Leng, Xueping
    Gao, Jiaming
    Huang, Danfei
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2024, 273
  • [29] EUCOMMIA ULMOIDES OLIV. EXTRACT REGULATES AGEs-INDUCED INJURY IN TUBULAR ENDOTHELIAL CELLS VIA THE RAGE-NRF2 PATHWAY
    Hur, Jinyoung
    Do, Moon Ho
    Kim, Mina
    Choi, Jiwon
    Kim, Yoonsook
    Ha, Sang Keun
    ACTA POLONIAE PHARMACEUTICA, 2019, 76 (04): : 683 - 690
  • [30] Protective effects of Etlingera elatior extract on lead acetate-induced changes in oxidative biomarkers in bone marrow of rats
    Haleagrahara, Nagaraja
    Jackie, Tan
    Chakravarthi, Srikumar
    Rao, Mallikarjuna
    Pasupathi, Thanikachalam
    FOOD AND CHEMICAL TOXICOLOGY, 2010, 48 (10) : 2688 - 2694