Renal structural changes and apelin receptor expression in spontaneously hypertensive rats: implications for hypertension-induced kidney injury.

adaptive mechanism apelin receptor chronic kidney disease hypertension renal damage

Journal

Folia morphologica
ISSN: 1644-3284
Titre abrégé: Folia Morphol (Warsz)
Pays: Poland
ID NLM: 0374620

Informations de publication

Date de publication:
11 Sep 2024
Historique:
received: 13 05 2024
accepted: 17 08 2024
revised: 16 08 2024
medline: 11 9 2024
pubmed: 11 9 2024
entrez: 11 9 2024
Statut: aheadofprint

Résumé

Arterial hypertension is a primary risk factor for kidney disease. Recent advances have implied a potential link between the apelin system and renal homeostasis. We used 6- and 12-month-old spontaneously hypertensive rats and age-matched normotensive controls to assess the changes in the renal expression of the apelin receptor by immunohistochemical method. The study also evaluated correlations between the renal apelin receptor's expression and renal injury indicators. The histological analysis showed elevated glomerular sclerosis and tubulointerstitial damage indices in both groups of hypertensive rats compared to age-matched controls. Older rats within each group exhibited higher scores than younger ones. The immunohistochemical analysis revealed varying apelin receptor expression patterns, with tubular expression intensifying both with hypertension severity and age. Glomerular expression was notably higher in older hypertensive rats compared to normotensive controls. We reported significant positive correlations between glomerular apelin receptor expression and glomerular sclerosis index in older hypertensive animals. Similarly, a positive correlation between tubular apelin receptor expression and tubulointerstitial damage index was discovered in hypertensive rats, suggesting hypertension-related changes in apelin receptor expression and renal damage. Our study found kidney changes and varying apelin receptor correlations in hypertensive rat kidneys, suggesting complex roles needing research.

Sections du résumé

BACKGROUND BACKGROUND
Arterial hypertension is a primary risk factor for kidney disease. Recent advances have implied a potential link between the apelin system and renal homeostasis.
MATERIALS AND METHODS METHODS
We used 6- and 12-month-old spontaneously hypertensive rats and age-matched normotensive controls to assess the changes in the renal expression of the apelin receptor by immunohistochemical method. The study also evaluated correlations between the renal apelin receptor's expression and renal injury indicators.
RESULTS RESULTS
The histological analysis showed elevated glomerular sclerosis and tubulointerstitial damage indices in both groups of hypertensive rats compared to age-matched controls. Older rats within each group exhibited higher scores than younger ones. The immunohistochemical analysis revealed varying apelin receptor expression patterns, with tubular expression intensifying both with hypertension severity and age. Glomerular expression was notably higher in older hypertensive rats compared to normotensive controls. We reported significant positive correlations between glomerular apelin receptor expression and glomerular sclerosis index in older hypertensive animals. Similarly, a positive correlation between tubular apelin receptor expression and tubulointerstitial damage index was discovered in hypertensive rats, suggesting hypertension-related changes in apelin receptor expression and renal damage.
CONCLUSIONS CONCLUSIONS
Our study found kidney changes and varying apelin receptor correlations in hypertensive rat kidneys, suggesting complex roles needing research.

Identifiants

pubmed: 39257194
pii: VM/OJS/J/100637
doi: 10.5603/fm.100637
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Stancho Stanchev (S)

Department of Anatomy, Histology and Embryology, Medical University of Sofia, Bulgaria, 2 'Zdrave' St., 1431 Sofia, Bulgaria. stanchev_1989@abv.bg.

Lyubomir Gaydarski (L)

Department of Anatomy, Histology and Embryology, Medical University of Sofia, Bulgaria, 2 'Zdrave' St., 1431 Sofia, Bulgaria.

Iva N Dimitrova (IN)

Department of Cardiology, University Hospital 'St. Ekaterina', Medical University of Sofia, Sofia, Bulgaria.

Georgi Kotov (G)

Clinic of Rheumatology, University Hospital 'St. Ivan Rilski', Department of Rheumatology, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria.

Boycho Landzhov (B)

Department of Anatomy, Histology and Embryology, Medical University of Sofia, Bulgaria, 2 'Zdrave' St., 1431 Sofia, Bulgaria.

Vidin Kirkov (V)

4Department of Health Policy and Management, Faculty of Public Health 'Prof. Dr. Tzekomir Vodenicharov', Medical University of Sofia, Sofia, Bulgaria.

Alexandar Iliev (A)

Department of Anatomy, Histology and Embryology, Medical University of Sofia, Bulgaria, 2 'Zdrave' St., 1431 Sofia, Bulgaria.

Classifications MeSH