Cornelian cherry extract ameliorates osteoporosis associated with hypercholesterolemia in New Zealand rabbits.


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:
Dec 2020
Historique:
entrez: 3 1 2021
pubmed: 4 1 2021
medline: 7 2 2021
Statut: ppublish

Résumé

Results of animal studies show that a high-cholesterol diet increases bone resorption and decreases bone formation, thus leading to osteoporosis. Previously, we reported on the beneficial influence of Cornelian cherry (Cornus mas L.) fruit on lipid profile in an animal model of diet-induced hipercholesterolemia. To investigate the influence of Cornus mas L. extract and loganic acid (LA) on cholesterol-induced bone changes. The study was conducted on 50 New Zealand rabbits. The animals were given either standard chow (group P) or the same standard chow enriched with 1% cholesterol (other groups). Additionally, the group CHOL+EX received Cornus mas L. extract, group CHOL+LA - loganic acid, and group CHOL+SIM - simvastatin. Serum concentration of bone turnover markers, bone mineral density (BMD) and bone micro-computed tomography (microCT) were assessed. In the CHOL group, a decrease in osteocalcin (OC) and an increase in C-terminated telopeptide of type I collagen (CTX) levels were detected (CHOL vs P 0.674 ±0.159 ng/mL vs 1.003 ±0.297 ng/mL and 10.049 ±1.276 ng/mL vs 7.721 ±1.187 ng/mL, respectively). The EX and LA ameliorated cholesterol-induced changes in serum OC (0.857 ±0.160 ng/mL and 1.103 ±0.356 ng/mL, respectively) and CTX (7.735 ±1.045 ng/mL and 8.128 ±1.106 ng/mL, respectively). There was a significant decrease in femoral BMD in CHOL group (0.429 ±0.11 g/cm² vs 0.449 ±0.020 g/cm²). The EX and LA ameliorated those changes (0.458 ±0.016 g/cm² and 0.449 ±0.021 g/cm², respectively). The microCT revealed increased bone volume ratio (BV/TV) and trabecular thickness (Tb.Th.) in the CHOL+EX group. Cornus mas L. inhibited bone resorption and stimulated bone formation, thereby preventing the development of cholesterol-induced osteoporosis.

Sections du résumé

BACKGROUND BACKGROUND
Results of animal studies show that a high-cholesterol diet increases bone resorption and decreases bone formation, thus leading to osteoporosis. Previously, we reported on the beneficial influence of Cornelian cherry (Cornus mas L.) fruit on lipid profile in an animal model of diet-induced hipercholesterolemia.
OBJECTIVES OBJECTIVE
To investigate the influence of Cornus mas L. extract and loganic acid (LA) on cholesterol-induced bone changes.
MATERIAL AND METHODS METHODS
The study was conducted on 50 New Zealand rabbits. The animals were given either standard chow (group P) or the same standard chow enriched with 1% cholesterol (other groups). Additionally, the group CHOL+EX received Cornus mas L. extract, group CHOL+LA - loganic acid, and group CHOL+SIM - simvastatin. Serum concentration of bone turnover markers, bone mineral density (BMD) and bone micro-computed tomography (microCT) were assessed.
RESULTS RESULTS
In the CHOL group, a decrease in osteocalcin (OC) and an increase in C-terminated telopeptide of type I collagen (CTX) levels were detected (CHOL vs P 0.674 ±0.159 ng/mL vs 1.003 ±0.297 ng/mL and 10.049 ±1.276 ng/mL vs 7.721 ±1.187 ng/mL, respectively). The EX and LA ameliorated cholesterol-induced changes in serum OC (0.857 ±0.160 ng/mL and 1.103 ±0.356 ng/mL, respectively) and CTX (7.735 ±1.045 ng/mL and 8.128 ±1.106 ng/mL, respectively). There was a significant decrease in femoral BMD in CHOL group (0.429 ±0.11 g/cm² vs 0.449 ±0.020 g/cm²). The EX and LA ameliorated those changes (0.458 ±0.016 g/cm² and 0.449 ±0.021 g/cm², respectively). The microCT revealed increased bone volume ratio (BV/TV) and trabecular thickness (Tb.Th.) in the CHOL+EX group.
CONCLUSIONS CONCLUSIONS
Cornus mas L. inhibited bone resorption and stimulated bone formation, thereby preventing the development of cholesterol-induced osteoporosis.

Identifiants

pubmed: 33389829
doi: 10.17219/acem/127683
doi:

Substances chimiques

Anthocyanins 0
Plant Extracts 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1389-1397

Auteurs

Beata Nowak (B)

Department of Pharmacology, Wroclaw Medical University, Poland.

Agnieszka Matuszewska (A)

Department of Pharmacology, Wroclaw Medical University, Poland.

Magadalena Tomanik (M)

Student's Scientific Club, Faculty of Mechanical Engineering, Wroclaw University of Science and Technology, Poland.

Jarosław Filipiak (J)

Faculty of Mechanical Engineering, Wroclaw University of Science and Technology, Poland.

Alicja Zofia Kucharska (AZ)

Department of Fruit, Vegetable and Plant Nutraceutical Technology, Wroclaw University of Environmental and Life Sciences, Poland.

Narcyz Piórecki (N)

Arboretum Bolestraszyce and Institute of Physiography, University of Rzeszow, Poland.

Diana Jędrzejuk (D)

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

Krzysztof Zduniak (K)

Department of Pathology, Wroclaw Medical University, Poland.

Małgorzata Trocha (M)

Department of Pharmacology, 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.

Tomasz Sozański (T)

Department of Pharmacology, Wroclaw Medical University, Poland.

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Classifications MeSH