326783

Histological Study to Compare the Effect of Atomoxetine Versus Formetrol on Dexamethasone-Induced Skeletal Muscle Atrophy in Male Mice

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Last updated: 20 Jan 2025

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Abstract

Introduction: Atrophy of skeletal muscles is still a serious clinical problem. Formoterol, an agonist of the B2- adrenergic receptor, may prevent this atrophy. An FDA-approved inhibitor of reuptake of norepinephrine called atomoxetine was effective in the prevention of skeletal muscle atrophy.
Aim of Work: Compare the effect of atomoxetine versus formetrol on dexamethasone-induced skeletal muscle atrophy in male mice.
Material and Methods: Forty-eight adult male albino mice were divided into six groups (8 mice each): Group 1 (control group) animals were injected intraperitoneally with 0.5ml sterile saline daily for seven days. Group 2 (dexamethasone treated group) animals were injected intraperitoneally with 10mg/kg/day dexamethasone for seven days to induce muscle atrophy. Group 3 (atomoxetine only treated group): animals received atomoxetine at a dose of 6mg/kg/day orally using insulin syringe without needle for seven days. Group 4 (atomoxetine + dexamethasone treated group): animals received both dexamethasone and atomoxetine at same doses and routes of administrationin as groups 2 and 3 respectively. Group 5 (formertrol only treated group): animals were injected intraperitoneally with 0.6 mg/kg/day formetrol for seven days. Group 6 (formertrol + dexamethasone treated group): animals received both dexamethasone and formetrol at same doses and routes of administration as groups 2 and 5 respectively. Sections were stained with hematoxylin and eosin stain & Picro Sirius red (PSR) histochemical reaction. Immunohistochemical staining was done using nuclear factor kappa-B (NF-κB) and heat shock protein (Hsp70). Area percent of collagen fibers deposition, area percent of nuclear factor kappa-B immunoexpression, area percent of heat shock protein 70 immunoexpression and diameter of muscle fiber were measured.
Results: Group 4 (atomoxetine and dexamethasone treated group) and Group 6 (formertrol and dexamethasone treated group) showed increase in diameter of muscle fibers as compared to dexamethasone group.
Conclusion: Formetrol has a potential role in preventing skeletal muscle atrophy.

DOI

10.21608/ejh.2023.240872.1958

Keywords

Atomoxetine, dexamethasone, formetrol, skeletal muscle atroph

Authors

First Name

Sarwat

Last Name

Ahmed

MiddleName

Lotfi

Affiliation

Histology and cell biology department, Faculty of medicine, Fayoum university

Email

sarlot23@gmail.com

City

cairo

Orcid

-

First Name

Heba

Last Name

Rashad

MiddleName

Essam

Affiliation

Histology and cell biology department, Faculty of medicine, Fayoum university

Email

hebaesam55@yahoo.com

City

fayoum

Orcid

-

First Name

Noha

Last Name

Ibrahim

MiddleName

Abd ellatif

Affiliation

Histology and cell biology department, Faculty of medicine, Fayoum university

Email

nohaabd33@gmail.com

City

giza

Orcid

-

First Name

Marwa

Last Name

Abd el all

MiddleName

Omar

Affiliation

Histology and cell biology department, Faculty of medicine, Fayoum university

Email

marwa88@gmail.com

City

fayoum

Orcid

-

First Name

Nehad

Last Name

Sadek

MiddleName

Ahmed

Affiliation

Histology and cell biology department, Faculty of medicine, Fayoum university

Email

nas04@fayoum.edu.eg

City

Giza

Orcid

-

Volume

47

Article Issue

4

Related Issue

52992

Issue Date

2024-12-01

Receive Date

2023-10-06

Publish Date

2024-12-01

Page Start

1,510

Page End

1,521

Print ISSN

1110-0559

Online ISSN

2090-2417

Link

https://ejh.journals.ekb.eg/article_326783.html

Detail API

http://journals.ekb.eg?_action=service&article_code=326783

Order

21

Type

Original Article

Type Code

119

Publication Type

Journal

Publication Title

Egyptian Journal of Histology

Publication Link

https://ejh.journals.ekb.eg/

MainTitle

Histological Study to Compare the Effect of Atomoxetine Versus Formetrol on Dexamethasone-Induced Skeletal Muscle Atrophy in Male Mice

Details

Type

Article

Created At

20 Jan 2025