Effects of efavirenz and tenofovir on bone tissue in Wistar rats.


Journal

Advances in clinical and experimental medicine : official organ Wroclaw Medical University
ISSN: 1899-5276
Titre abrégé: Adv Clin Exp Med
Pays: Poland
ID NLM: 101138582

Informations de publication

Date de publication:
11 2020
Historique:
entrez: 3 12 2020
pubmed: 4 12 2020
medline: 26 1 2021
Statut: ppublish

Résumé

Clinical trials indicate an increased risk of osteoporosis and bone fractures in people infected with human immunodeficiency virus (HIV). The pathogenesis of bone disturbances in HIV-positive patients is unknown, but it is suggested that antiretroviral drugs may be involved. To assess the effects of efavirenz (EF) and tenofovir (T) on bone remodeling in rats. The study involved 36 male Wistar rats divided into 3 groups, receiving normal saline (control group - group C), efavirenz (group EF) or tenofovir disoproxil (group T). After 24 weeks of the study, the following observations were made: In blood serum of the EF group compared to group C, there were increased levels of tartrate-resistant acid phosphatase form 5b (TRAP) and inorganic phosphorus. In the densitometric examination, group T showed a lower total body (TB) bone mineral density (BMD) than group C. In the immunohistochemical assessment, group EF showed a higher intensity and extension of anti-tartrate resistant acid phosphatase antibodies (abTRAP) compared to group C. In the histopathological examination of the second lumbar vertebra (L2), group EF showed a lower bone surface/volume ratio (BS/BV) and higher trabecular thickness (Tb.Th) than the control group. In the histopathological examination of the femur, a lower bone surface/tissue volume (BS/TV) and lower trabecular number (Tb.N) were found in group T compared to in group C. A lower value of the Young's modulus was observed in the four-point bending trial in groups EF and T compared to group C. The results of this study indicate that EF affects bone microarchitecture and leads to impaired biomechanical properties of bones in rats. Additionally, the negative effect of T on bone tissue was confirmed.

Sections du résumé

BACKGROUND
Clinical trials indicate an increased risk of osteoporosis and bone fractures in people infected with human immunodeficiency virus (HIV). The pathogenesis of bone disturbances in HIV-positive patients is unknown, but it is suggested that antiretroviral drugs may be involved.
OBJECTIVES
To assess the effects of efavirenz (EF) and tenofovir (T) on bone remodeling in rats.
MATERIAL AND METHODS
The study involved 36 male Wistar rats divided into 3 groups, receiving normal saline (control group - group C), efavirenz (group EF) or tenofovir disoproxil (group T).
RESULTS
After 24 weeks of the study, the following observations were made: In blood serum of the EF group compared to group C, there were increased levels of tartrate-resistant acid phosphatase form 5b (TRAP) and inorganic phosphorus. In the densitometric examination, group T showed a lower total body (TB) bone mineral density (BMD) than group C. In the immunohistochemical assessment, group EF showed a higher intensity and extension of anti-tartrate resistant acid phosphatase antibodies (abTRAP) compared to group C. In the histopathological examination of the second lumbar vertebra (L2), group EF showed a lower bone surface/volume ratio (BS/BV) and higher trabecular thickness (Tb.Th) than the control group. In the histopathological examination of the femur, a lower bone surface/tissue volume (BS/TV) and lower trabecular number (Tb.N) were found in group T compared to in group C. A lower value of the Young's modulus was observed in the four-point bending trial in groups EF and T compared to group C.
CONCLUSIONS
The results of this study indicate that EF affects bone microarchitecture and leads to impaired biomechanical properties of bones in rats. Additionally, the negative effect of T on bone tissue was confirmed.

Identifiants

pubmed: 33269812
doi: 10.17219/acem/127684
doi:

Substances chimiques

Alkynes 0
Benzoxazines 0
Cyclopropanes 0
Tenofovir 99YXE507IL
efavirenz JE6H2O27P8

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1265-1275

Auteurs

Agnieszka Matuszewska (A)

Department of Pharmacology, Wroclaw Medical University, Poland.

Beata Nowak (B)

Department of Pharmacology, Wroclaw Medical University, Poland.

Anna Nikodem (A)

Division of Biomedical Engineering and Experimental Mechanics, Wroclaw University of Technology, Poland.

Diana Jędrzejuk (D)

Department of Endocrinology, Diabetes and Isotope Therapy, Wroclaw Medical University, Poland.

Danuta Szkudlarek (D)

Department of Pathology, Wroclaw Medical University, Poland.

Krzysztof Zduniak (K)

Department of Pathology, Wroclaw Medical University, Poland.

Jarosław Filipiak (J)

Division of Biomedical Engineering and Experimental Mechanics, Wroclaw University of Technology, Poland.

Marta Sznadruk-Bender (M)

Department of Pharmacology, Wroclaw Medical University, Poland.

Tomasz Tomkalski (T)

Department of Endocrinology, T. Marciniak Lower Silesian Specialist Hospital, Poland.

Ireneusz Ceremuga (I)

Department of Medical Biochemistry, Wroclaw Medical University, Poland.

Marek Bolanowski (M)

Department of Endocrinology, Diabetes and Isotope Therapy, Wroclaw Medical University, Poland.

Adam Szeląg (A)

Department of Pharmacology, Wroclaw Medical University, Poland.

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Classifications MeSH