Seminal plasma metabolomics profiles following long (4-7 days) and short (2 h) sexual abstinence periods.

Metabolomics Nuclear magnetic resonance spectroscopy Sexual abstinence Sperm motility

Journal

European journal of obstetrics, gynecology, and reproductive biology
ISSN: 1872-7654
Titre abrégé: Eur J Obstet Gynecol Reprod Biol
Pays: Ireland
ID NLM: 0375672

Informations de publication

Date de publication:
Sep 2021
Historique:
received: 29 03 2021
revised: 08 07 2021
accepted: 12 07 2021
pubmed: 30 7 2021
medline: 22 9 2021
entrez: 29 7 2021
Statut: ppublish

Résumé

Metabolomic profiling of seminal plasma has been suggested as a possible approach for a fast and non-invasive male infertility evaluation diagnosis. However, metabolomics profiles in normozoospermic men have not been thoroughly investigated, and the influence of ejaculation-abstinence has not been described. To provide interim reference values and find associations between the metabolomics profiles of human seminal plasma and length of ejaculation-abstinence period in normozoospermic men. Semen samples collected after long (4-7 days) and short abstinence (2 h) from 31 normozoospermic males were assessed for routine quality parameters before the seminal plasma was separated by centrifugation. Metabolomics profiles of the seminal plasma were then determined using untargeted Nuclear Magnetic Resonance Spectroscopy. In total, 30 metabolites were identified. Pyruvate showed a higher concentration, while fructose, acetate, choline, methanol, N-acetylglucosamine, O-acetylcarnitine, uridine, and sn-glycero-3-phosphocoline showed lower concentrations in samples collected after short abstinence (vs. long). All metabolites showed lower absolute amounts (volume × concentration) following shorter abstinence. However, the lower sperm concentration in samples collected after short abstinence resulted in higher absolute amounts of pyruvate and taurine per spermatozoa: pyruvate 1.92 (1.12-3.87) vs. 1.29 (0.83-2.62) (P < 0.001) and taurine 0.58 (0.36-0.92) vs. 0.43 (0.28-0.95) (P < 0.05) ng/10 The generally lower concentrations of seminal metabolites after short abstinence periods may be related to the shorter time available for secretion and collection of these metabolites by the accessory glands and the epididymides. The concomitant lower number of spermatozoa in the second ejaculate resulted in increased absolute amounts of pyruvate and taurine per spermatozoa, accompanied by increased spermatozoa motility in these samples. The simultaneous increase in percentages of motile spermatozoa and absolute amounts of pyruvate and taurine per spermatozoa after shorter abstinence might indicate that these two metabolites play a more critical role in sperm motility, which should be further investigated in future studies.

Identifiants

pubmed: 34325212
pii: S0301-2115(21)00367-5
doi: 10.1016/j.ejogrb.2021.07.024
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

178-183

Informations de copyright

Copyright © 2021 The Author(s). Published by Elsevier B.V. All rights reserved.

Auteurs

H Alipour (H)

Department of Health Science and Technology, Regenerative Medicine Group, Aalborg University, Aalborg, Denmark. Electronic address: hiva@hst.aau.dk.

R K Duus (RK)

Department of Health Science and Technology, Regenerative Medicine Group, Aalborg University, Aalborg, Denmark.

R Wimmer (R)

Department of Chemistry and Bioscience, Aalborg University, Aalborg, Denmark.

F Dardmeh (F)

Department of Health Science and Technology, Regenerative Medicine Group, Aalborg University, Aalborg, Denmark.

S S Du Plessis (SS)

Department of Basic Medical Sciences, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates; Division of Medical Physiology, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.

N Jørgensen (N)

University Department of Growth and Reproduction and International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, Copenhagen, Denmark.

O B Christiansen (OB)

Department of Obstetrics and Gynecology, Fertility Unit, Aalborg University Hospital, Aalborg, Denmark; Institute of Clinical Medicine, Aalborg University, Denmark.

C Hnida (C)

Department of Obstetrics and Gynecology, Fertility Unit, Aalborg University Hospital, Aalborg, Denmark.

H I Nielsen (HI)

Department of Health Science and Technology, Regenerative Medicine Group, Aalborg University, Aalborg, Denmark.

G Van Der Horst (G)

Department of Medical Biosciences, University of the Western Cape, Cape Town, South Africa.

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