Piper sarmentosum Effects on 11β-Hydroxysteroid Dehydrogenase Type 1 Enzyme in Serum and Bone in Rat Model of Glucocorticoid-Induced Osteoporosis
Glucocorticoid-induced osteoporosis is one of the common causes of secondary osteoporosis. ( ) extract possesses antioxidant and anti-inflammatory activities. In this study, we determined the correlation between the effects of leaf water extract with the regulation of 11β-hydroxysteroid dehydrogenas...
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Published in | Molecules (Basel, Switzerland) Vol. 21; no. 11; p. 1523 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI
15.11.2016
MDPI AG |
Subjects | |
Online Access | Get full text |
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Summary: | Glucocorticoid-induced osteoporosis is one of the common causes of secondary osteoporosis.
(
) extract possesses antioxidant and anti-inflammatory activities. In this study, we determined the correlation between the effects of
leaf water extract with the regulation of 11β-hydroxysteroid dehydrogenase (HSD) type 1 enzyme activity in serum and bone of glucocorticoid-induced osteoporotic rats. Twenty-four Sprague-Dawley rats were grouped into following: G1: sham-operated group administered with intramuscular vehicle olive oil and vehicle normal saline orally; G2: adrenalectomized (adrx) control group given intramuscular dexamethasone (120 μg/kg/day) and vehicle normal saline orally; G3: adrx group given intramuscular dexamethasone (120 μg/kg/day) and water extract of
(125 mg/kg/day) orally. After two months, the femur and serum were taken for ELISA analysis. Results showed that
leaf water extract significantly reduced the femur corticosterone concentration (
< 0.05). This suggests that
leaf water extract was able to prevent bone loss due to long-term glucocorticoid therapy by acting locally on the bone cells by increasing the dehydrogenase action of 11β-HSD type 1. Thus,
may have the potential to be used as an alternative medicine against osteoporosis and osteoporotic fracture in patients on long-term glucocorticoid treatment. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1420-3049 1420-3049 |
DOI: | 10.3390/molecules21111523 |