Other language title :
اﺛﺮ ﮔﻠﻮﻛﻮ ﻛﻮرﺗﻴﻜﻮﺋﻴﺪ ﺑﺮ ﻧﺸﺎﻧﮕﺮﻫﺎي ﻣﺘﺎﺑﻮﻟﻴﺴﻢ اﺳﺘﺨﻮان و ﭼﮕﺎﻟﻲ ﻣﻌﺪﻧﻲ اﺳﺘﺨﻮان Rat
Title of article :
Effects of Glucocorticoid on Bone Metabolism Markers and Bone Mineral Density in Rats
Author/Authors :
Sobhani, A Department of Anatomy - Faculty of Medicine - Tehran University of Medical Sciences , Moradi, F Department of Anatomy - Faculty of Medicine - Tehran University of Medical Sciences , Pasbakhsh, P Department of Anatomy - Faculty of Medicine - Tehran University of Medical Sciences , Ansari, M Department of Biochemistry - Faculty of Medicine - Tehran University of Medical Sciences , Moghadasi, M Department of Rheumatology - Sina Hospital - Faculty of Medicine - Tehran University of Medical , Ragard Kashani, I Department of Anatomy - Faculty of Medicine - Tehran University of Medical Sciences
Abstract :
Statement of Problem: Glucocorticoid-induced osteoporosis is characterized by a decrease in osteoblast numbers and a marked impairment of new bone formation. Purpose: The ain of present study was to evaluate the effect of methylprednisolone acetate on bone metabolism and bone mineral density in rats. Materials and Methods: Eighteen male Sprague Dawley rats (8 weeks old, weighting 180 gm) were randomly divided into three groups: Group A (n=6), was a baseline control consisting of normal animals. Group B (n=6), was treated only by normal saline injection (0.9%) and group C (n=6), injected Methylprednisolone acetate (0.2 mg/kg/s.c. 3 times/week for 4 weeks). Changes in biochemical agents of serum calcium were evaluated by measuring acid phosphatase and osteocalcin, before and after treatment. Bone mineral density (BMD) of the lumbar vertebrae was also measured by dual energy x-ray absorptiometry (DEXA). Results: The results showed that, serum calcium levels were not affected by methylprednisolone acetate (p>0.05), but acid phosphatase levels of serum increased significantly (p≤0.05). In addition, the serum osteocalcin levels and bone mineral density of lumbar vertebrae decreased significantly (p≤0.05) in the methylprednisolone acetate-treated group as compared to the other groups. Conclusions: The findings indicate that administration of methylprednisolone acetate decreases bone formation and increases bone resorption in the lumbar vertebrae.
Farsi abstract :
ﺑﻴﺎن ﻣﺴﺄﻟﻪ: ﺍﺳﺘﺌﻮﭘﺮﻭﺯ ﻧﺎﺷﻲ ﺍﺯ ﮔﻠﻮﻛﻮ ﻛﻮﺭﺗﻴﻜﻮﺋﻴـﺪﻫﺎ ﺑـﻪ ﺻـﻮﺭﺕ ﻛـﺎﻫﺶ ﺩﺭ ﺗﻌـﺪﺍﺩ ﺍﺳﺘﺌﻮﺑﻼﺳـﺖ ﻫـﺎ ﻭ ﻧﻘـﺎﻳﺺ ﻣـﺸﺨﺺ ﺳـﺎﺧﺘﻤﺎﻧﻲ ﺩﺭ ﺍﺳﺘﺨﻮﺍﻧﻬﺎﻱ ﺟﺪﻳﺪ ﻣﺸﺨﺺ ﻣﻲ ﺷﻮﺩ.
ﻫﺪف: ﻣﻄﺎﻟﻌﻪ ﺣﺎﺿﺮ ﺑﺎ ﻫﺪﻑ ﺗﻌﻴﻴﻦ ﺍﺛﺮ ﻣﺘﻴﻞ ﭘﺮﺩﻧﻴﺰﻭﻟﻮﻥ ﺍﺳﺘﺎﺕ ﺑﺮ ﻣﺘﺎﺑﻮﻟﻴﺴﻢ ﻭ ﭼﮕﺎﻟﻲ ﻣﻌﺪﻧﻲ ﺍﺳﺘﺨﻮﺍﻥ Rat ﺍﻧﺠﺎﻡ ﺷﺪ.
روش ﺗﺤﻘﻴﻖ: ﺗﻌﺪﺍﺩ 18 Rat ﻧﺮ ﺍﺯ ﻧﮋﺍﺩ Sprague Dawley (ﺑﺎ ﺳﻦ 8 ﻫﻔﺘﻪ ﻭ ﻭﺯﻥ ﺣﺪﻭﺩ 180 ﮔﺮﻡ) ﺑـﻪ ﻃـﻮﺭ ﺗـﺼﺎﺩﻓﻲ ﺑـﻪ ﺳـﻪ ﮔـﺮﻭﻩ 6 ﺗﺎﻳﻲ ﺗﻘﺴﻴﻢ ﺷﺪﻧﺪ. ﮔﺮﻭﻩ A )ﺷﺎﻫﺪ( ﺷﺎﻣﻞ ﻧﻤﻮﻧﻪ ﻫﺎﻱ ﺳﺎﻟﻢ ﺣﻴﻮﺍﻧﻲ ﺑﻮﺩ. ﺩﺭ ﮔﺮﻭﻩ B ﺗﺰﺭﻳﻖ ﻧﺮﻣـﺎﻝ ﺳـﺎﻟﻴﻦ ﺍﻧﺠـﺎﻡ ﺷـﺪ ﻭ ﺩﺭ ﮔـﺮﻭﻩC ﻧﻴـﺰ ﻣﺘﻴﻞ ﭘﺮﺩﻧﻴﺰﻭﻟﻮﻥ ﺯﻳﺮﭘﻮﺳﺘﻲ ﺑﻪ ﻣﺪﺕ4 ﻫﻔﺘﻪ ﻭ3 ﺑﺎﺭ ﺩﺭ ﻫﻔﺘﻪ ﺑﻪ ﻣﻴﺰﺍﻥ0/2 ﻣﻴﻠﻴﮕﺮﻡ ﺑﻪ ﺍﺯﺍﻱ ﻫﺮ ﻛﻴﻠﻮﮔﺮﻡ ﻭﺯﻥ ﺣﻴﻮﺍﻥ ﺗﺰﺭﻳﻖ ﺷـﺪ. ﺗﻐﻴﻴـﺮﺍﺕ ﻋﻮﺍﻣﻞ ﺑﻴﻮﺷﻴﻤﻴﺎﻳﻲ ﻛﻠ ﺴﻴﻢ ﺳﺮﻡ، ﺍﺳﻴﺪ ﻓﺴﻔﺎﺗﺎﺯ ﻭ ﺍﺳﺘﺌﻮﻛﻠﺴﻴﻦ ﺑﺎ ﺍﻧﺪﺍﺯﻩ ﮔﻴﺮﻱ ﻗﺒﻞ ﻭ ﺑﻌﺪ ﺍﺯ ﺩﺭﻣـﺎﻥ ﻣﻘﺎﻳـﺴﻪ ﺷـﺪ ﭼﮕـﺎﻟﻲ ﻣﻌـﺪﻧﻲ ﺍﺳـﺘﺨﻮﺍﻥ (BMD) ﻣﻬﺮﻩ ﻫﺎﻱ ﻛﻤﺮﻱ ﺑﺎ ﺍﺳﺘﻔﺎﺩﻩ ﺍﺯ ﺭﻭﺵ (Dual Energy X ray Absorptiometry (DEXA ﺗﻌﻴﻴﻦ ﺷﺪ.
ﻳﺎﻓﺘﻪ ﻫﺎ: ﺳﻄﺢ ﻛﻠﺴﻴﻢ ﺳﺮﻡ ، ﺗﺤﺖ ﺗﺄﺛﻴﺮ ﻣﺘﻴﻞ ﭘﺮﺩﻧﻴﺰﻭﻟﻮﻥ ﺍﺳﺘﺎﺕ ﺗﻐﻴﻴﺮ ﻧﻴﺎﻓﺖ (P>0/05)، ﺍﻣﺎ ﺍﺳﻴﺪ ﻓﺴﻔﺎﺗﺎﺯ ﺳﺮﻡ ﺑﻪ ﻃﻮﺭ ﻣﻌني ﺩﺍﺭﻱ ﺍﻓﺰﺍﻳﺶ ﻧﺸﺎﻥ ﺩﺍﺩ (P<0/05). ﺳﻄﺢ ﺍﺳﺘﺌﻮﻛﻠﺴﻴﻦ ﺳﺮﻣﻲ ﻭ ﭼﮕﺎﻟﻲ ﻣﻌﺪﻧﻲ ﺍﺳﺘﺨﻮﺍﻥ ﺩﺭ ﻧﺎﺣﻴﻪ ﻣﻬﺮﻩ ﻫﺎﻱ ﻛﻤﺮﻱ ﺑﻪ ﻃـﻮﺭ ﻣﻌﻨـﻲ ﺩﺍﺭﻱ ﺩﺭ ﮔـﺮﻭﻩ ﻣﺘﻴـﻞ ﭘﺮﺩﻧﻴﺰﻭﻟﻮﻥ ﺍﺳﺘﺎﺕ ﻛﺎﻫﺶ ﻳﺎﻓﺖ (P<0/05).
ﻧﺘﻴﺠﻪ ﮔﻴﺮي: ﺑﺮ ﺍﺳﺎﺱ ﻧﺘﺎﻳﺞ ﺣﺎﺻﻞ ﺍﺯ ﺍﻳﻦ ﺗﺤﻘﻴﻖ ﻣﻲ ﺗﻮﺍﻥ ﺍﺫﻋﺎﻥ ﻛﺮﺩ ﻛﻪ ﺗﺠﻮﻳﺰ ﻣﺘﻴﻞ ﭘﺮﺩﻧﻴﺰﻭﻟﻮﻥ ﺍﺳـﺘﺎﺕ، ﺳـﺒﺐ ﻛـﺎﻫﺶ ﺷـﻜﻞ گيـﺮﻱ ﺍﺳﺘﺨﻮﺍﻥ ﻭ ﺍﻓﺰﺍﻳﺶ ﺗﺤﻠﻴﻞ ﺍﺳﺘﺨﻮﺍﻥ ﻣﻬﺮﻩ ﻫﺎﻱ ﻛﻤﺮﻱ ﻣﻲ ﺷﻮﺩ.
Keywords :
Glucocorticoid , Osteoporosis , Bone metabolism markers , BMD
Journal title :
Astroparticle Physics