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Evaluating the therapeutic effect of Diallyl disulfide compared to that of Alderonate on Glucocorticoids induced osteoporosis in rats: Biochemical and histomorphometric analysis

Article

Last updated: 24 Dec 2024

Subjects

-

Tags

Comparative Physiology

Abstract

Introduction: The prevalence of Glucocorticoids (GC) use made Glucocorticoid induced osteoporosis (GIO) an important form of secondary osteoporosis. Bisphosphonates (Alderonate) are considered as pharmacological agents in prevention and treatment of GIO. Garlic containing Diallyl disulfide (DAS) has received special attention for its beneficial effects as an antioxidant. The present study attempted to evaluate the Alendronate, DAS, and the combination of Alderonate and DAS effect on bone gene expression of RANKL and OPG, serum biochemical parameters [Ca, P, alkaline phosphatase (ALP)] and histological assessment of tibia in animal model of GIO.

Material and Method: Fifty pathogen albino male rats were allocated in five groups:Control group(C), Methyl prednisolone group (M), methyl prednisolone Aldenronate group (A) Methyl prednisolone Diallyl disulfide (D), Diallyl disulfide Alendronate Methyl prednisolone (AD) group.Gene expression studies, biochemical parameters, histological and morphometric studies were assessed for all animals.

Results: Among the study groups, Methyl prednisolone exposure provoked decrease in OPG (0.26±0.16) increase in RANKL (3.57±.39) gene expression, decrease in serum ALP(85.38±6.3),Ca(6.41±0.89), P(1.9 ±0.35) levels and decrease in trabecular thickness (57.01±23.22).Alderonate and Dially disulfide concomitant administration was shown to increase OPG(2.84 ±0.53)and decrease in RANKL (0.63 ± 0.27) gene expression, increase serum ALP(187.75±24.93),Ca(10.330 ±.69)and P(3.16 ±0.43) levels,increase trabecular thickness(154.7±31.7)(p < 0.001).

Conclusion: Diallyl disulfide can add advantage to Alderonate in treatment of glucocorticoid induced osteoprosis.

DOI

10.21608/besps.2019.6704.1011

Keywords

Osteoporosis, Alendronate, Diallyl disulfide, OPG, RANKL

Authors

First Name

Noha

Last Name

Badae

MiddleName

-

Affiliation

Physiology,Faculty of medicine, Alexandria University

Email

dr.nohabadi3@yahoo.com

City

Alexandria

Orcid

-

First Name

Rasha

Last Name

Ghazala

MiddleName

Abdelmawla

Affiliation

Medical Biochemistry department, Faculty of Medicine, Alexandria University

Email

dr_rashaghazala@yahoo.com

City

-

Orcid

-

First Name

Eiman

Last Name

Zaki

MiddleName

Ibrahim

Affiliation

Histology and Cell Biology department, Faculty of Medicine, Alexandria University

Email

eimaniazaki@gmail.com

City

Alexandria

Orcid

-

First Name

Suzan

Last Name

Abdel-Ghani

MiddleName

Awad

Affiliation

Clinical pharmacology department, Faculty of Medicine, Alexandria University

Email

s.awad.morsy@gmail.com

City

Alexandria

Orcid

-

Volume

39

Article Issue

2

Related Issue

5052

Issue Date

2019-12-01

Receive Date

2018-12-16

Publish Date

2019-12-01

Page Start

129

Page End

142

Print ISSN

1110-0842

Online ISSN

2356-9514

Link

https://besps.journals.ekb.eg/article_28980.html

Detail API

https://besps.journals.ekb.eg/service?article_code=28980

Order

1

Type

Original Article

Type Code

567

Publication Type

Journal

Publication Title

Bulletin of Egyptian Society for Physiological Sciences

Publication Link

https://besps.journals.ekb.eg/

MainTitle

Evaluating the therapeutic effect of Diallyl disulfide compared to that of Alderonate on Glucocorticoids induced osteoporosis in rats: Biochemical and histomorphometric analysis

Details

Type

Article

Created At

22 Jan 2023