NLRP3 Inflammasome: A New Pharmacological Target for Reducing Testicular Damage Associated with Varicocele.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
28 Jan 2021
Historique:
received: 08 01 2021
revised: 25 01 2021
accepted: 26 01 2021
entrez: 2 2 2021
pubmed: 3 2 2021
medline: 4 9 2021
Statut: epublish

Résumé

Many bioactive natural compounds are being increasingly used for therapeutics and nutraceutical applications to counteract male infertility, particularly varicocele. The roles of selenium and Polydeoxyribonucleotide (PDRN) were investigated in an experimental model of varicocele, with particular regard to the role of NLRP3 inflammasome. Male rats underwent sham operation and were daily administered with vehicle, seleno-L-methionine (Se), PDRN, and with the association Se-PDRN. Another group of rats were operated for varicocele. After twenty-eight days, sham and varicocele rats were sacrificed and both testes were weighted and analyzed. All the other rats were challenged for one month with the same compounds. In varicocele animals, lower testosterone levels, testes weight, NLRP3 inflammasome, IL-1β and caspase-1 increased gene expression were demonstrated. TUNEL assay showed an increased number of apoptotic cells. Structural and ultrastructural damage to testes was also shown. PDRN alone significantly improved all considered parameters more than Se. The Se-PDRN association significantly improved all morphological parameters, significantly increased testosterone levels, and reduced NLRP3 inflammasome, caspase-1 and IL-1β expression and TUNEL-positive cell numbers. Our results suggest that NLRP3 inflammasome can be considered an interesting target in varicocele and that Se-PDRN may be a new medical approach in support to surgery.

Identifiants

pubmed: 33525681
pii: ijms22031319
doi: 10.3390/ijms22031319
pmc: PMC7865407
pii:
doi:

Substances chimiques

IL1B protein, mouse 0
Interleukin-1beta 0
NLR Family, Pyrin Domain-Containing 3 Protein 0
Nlrp3 protein, mouse 0
Polydeoxyribonucleotides 0
Testosterone 3XMK78S47O
Selenomethionine 964MRK2PEL
Casp1 protein, mouse EC 3.4.22.36
Caspase 1 EC 3.4.22.36

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Pietro Antonuccio (P)

Department of Human Pathology of Adult and Childhood "Gaetano Barresi", University of Messina, 98125 Messina, Italy.

Antonio Girolamo Micali (AG)

Department of Biomedical, Dental, Morphological and Functional Imaging Sciences, University of Messina, 98125 Messina, Italy.

Carmelo Romeo (C)

Department of Human Pathology of Adult and Childhood "Gaetano Barresi", University of Messina, 98125 Messina, Italy.

Jose Freni (J)

Department of Biomedical, Dental, Morphological and Functional Imaging Sciences, University of Messina, 98125 Messina, Italy.

Giovanna Vermiglio (G)

Department of Biomedical, Dental, Morphological and Functional Imaging Sciences, University of Messina, 98125 Messina, Italy.

Domenico Puzzolo (D)

Department of Biomedical, Dental, Morphological and Functional Imaging Sciences, University of Messina, 98125 Messina, Italy.

Francesco Squadrito (F)

Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.

Natasha Irrera (N)

Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.

Herbert R Marini (HR)

Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.

Rosa Alba Rana (RA)

Department of Medicine and Aging Sciences, University G. d'Annunzio, Chieti and Pescara, 66100 Chieti, Italy.

Giovanni Pallio (G)

Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.

Letteria Minutoli (L)

Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.

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Classifications MeSH