Zinc oxide and selenium nanoparticles can improve semen quality and heat shock protein expression in cryopreserved goat (Capra hircus) spermatozoa.


Journal

Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS)
ISSN: 1878-3252
Titre abrégé: J Trace Elem Med Biol
Pays: Germany
ID NLM: 9508274

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 28 02 2023
revised: 23 07 2023
accepted: 28 08 2023
medline: 3 11 2023
pubmed: 3 9 2023
entrez: 2 9 2023
Statut: ppublish

Résumé

Reactive oxygen species (ROS) are strongly linked with oxidative stress (OS) generated during the process of sperm cryopreservation. Indeed, cellular damage from ROS has been implicated during sperm cryopreservation which causes deterioration in sperm quality and antioxidant nanoparticles (NPs) have been successful in preventing such damage. The interaction of NPs with sperm cells has been less frequently explored in farm animals. The present study explored the effect of NP supplementation on sperm ultrastructure, potential interaction with sperm membrane (plasma and acrosome membrane), heat shock protein (HSP) gene expression levels and sperm quality in cryopreserved buck semen. Thirty-two (32) ejaculates were collected from four (4) adult male bucks and then diluted in Tris- citric acid- fructose- egg yolk (TCFY) extender containing the Zinc-oxide (ZnO) and Selenium (Se) NP treatments (T0: Control; TZn: 0.1 mg/mL ZnO NPs and TSe: 1 µg/mL Se NPs) after initial evaluation. Diluted semen was packed in 0.25 mL French mini straws and then stored in liquid nitrogen (LN We found a significant (p < 0.05) increase in the percentage of spermatozoa with intact plasma membrane, and intact acrosome in the ZnO (0.1 mg/mL) and Se (1 µg/mL) NP supplemented groups in comparison to the frozen control group. TEM assessment revealed no internalization of both ZnO and Se NPs into the sperm structure. Few occasional contacts of ZnO NPs with the sperm membrane and a few agglomerates of Se NPs around the area of damaged membranes were visualized. HSP70 and HSP90 mRNA levels were significantly (p < 0.001) higher in the NP supplemented groups in comparison to the control. HSP70 and HSP90 mRNA levels had a strong positive association with sperm motility and a weak to moderate association with other sperm parameters. Current findings indicated that ZnO NPs are more potent than Se NPs in ameliorating peroxidative damages during sperm cryopreservation, increases semen quality parameters possibly by increasing the expression levels of HSP genes in buck semen. Furthermore, NP supplementation may have a potential role in preserving sperm head ultrastructure by acting as an antioxidant and reducing OS during various degrees of cellular insults, which needs to be further explored.

Sections du résumé

BACKGROUND BACKGROUND
Reactive oxygen species (ROS) are strongly linked with oxidative stress (OS) generated during the process of sperm cryopreservation. Indeed, cellular damage from ROS has been implicated during sperm cryopreservation which causes deterioration in sperm quality and antioxidant nanoparticles (NPs) have been successful in preventing such damage. The interaction of NPs with sperm cells has been less frequently explored in farm animals.
OBJECTIVE OBJECTIVE
The present study explored the effect of NP supplementation on sperm ultrastructure, potential interaction with sperm membrane (plasma and acrosome membrane), heat shock protein (HSP) gene expression levels and sperm quality in cryopreserved buck semen.
MATERIALS AND METHODS METHODS
Thirty-two (32) ejaculates were collected from four (4) adult male bucks and then diluted in Tris- citric acid- fructose- egg yolk (TCFY) extender containing the Zinc-oxide (ZnO) and Selenium (Se) NP treatments (T0: Control; TZn: 0.1 mg/mL ZnO NPs and TSe: 1 µg/mL Se NPs) after initial evaluation. Diluted semen was packed in 0.25 mL French mini straws and then stored in liquid nitrogen (LN
RESULTS RESULTS
We found a significant (p < 0.05) increase in the percentage of spermatozoa with intact plasma membrane, and intact acrosome in the ZnO (0.1 mg/mL) and Se (1 µg/mL) NP supplemented groups in comparison to the frozen control group. TEM assessment revealed no internalization of both ZnO and Se NPs into the sperm structure. Few occasional contacts of ZnO NPs with the sperm membrane and a few agglomerates of Se NPs around the area of damaged membranes were visualized. HSP70 and HSP90 mRNA levels were significantly (p < 0.001) higher in the NP supplemented groups in comparison to the control. HSP70 and HSP90 mRNA levels had a strong positive association with sperm motility and a weak to moderate association with other sperm parameters.
CONCLUSIONS CONCLUSIONS
Current findings indicated that ZnO NPs are more potent than Se NPs in ameliorating peroxidative damages during sperm cryopreservation, increases semen quality parameters possibly by increasing the expression levels of HSP genes in buck semen. Furthermore, NP supplementation may have a potential role in preserving sperm head ultrastructure by acting as an antioxidant and reducing OS during various degrees of cellular insults, which needs to be further explored.

Identifiants

pubmed: 37659125
pii: S0946-672X(23)00172-4
doi: 10.1016/j.jtemb.2023.127296
pii:
doi:

Substances chimiques

Zinc Oxide SOI2LOH54Z
Selenium H6241UJ22B
Antioxidants 0
Heat-Shock Proteins 0
Reactive Oxygen Species 0
HSP70 Heat-Shock Proteins 0
RNA, Messenger 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

127296

Informations de copyright

Copyright © 2023 Elsevier GmbH. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Sayed Nabil Abedin (SN)

College of Veterinary Science, Assam Agricultural University, Guwahati, India.

Anubha Baruah (A)

College of Veterinary Science, Assam Agricultural University, Guwahati, India.

Kishore Kumar Baruah (KK)

Division of Animal and Fisheries Science, Indian Council of Agricultural Research (ICAR) Research Complex for North Eastern Hill Region, Meghalaya, India.

Arundhati Bora (A)

College of Veterinary Science, Assam Agricultural University, Guwahati, India.

Devo Jyoti Dutta (DJ)

College of Veterinary Science, Assam Agricultural University, Guwahati, India.

Govindasamy Kadirvel (G)

Division of Animal and Fisheries Science, Indian Council of Agricultural Research (ICAR) Research Complex for North Eastern Hill Region, Meghalaya, India.

Rahul Katiyar (R)

Division of Animal and Fisheries Science, Indian Council of Agricultural Research (ICAR) Research Complex for North Eastern Hill Region, Meghalaya, India.

Sunil Doley (S)

Division of Animal and Fisheries Science, Indian Council of Agricultural Research (ICAR) Research Complex for North Eastern Hill Region, Meghalaya, India.

Samir Das (S)

Division of Animal and Fisheries Science, Indian Council of Agricultural Research (ICAR) Research Complex for North Eastern Hill Region, Meghalaya, India.

Gautam Khargharia (G)

Division of Animal and Fisheries Science, Indian Council of Agricultural Research (ICAR) Research Complex for North Eastern Hill Region, Meghalaya, India.

Biplab Sarkar (B)

Indian Institute of Agricultural Biotechnology, Ranchi, India.

Sudip Sinha (S)

College of Veterinary Science, Assam Agricultural University, Guwahati, India.

Arundhati Phookan (A)

College of Veterinary Science, Assam Agricultural University, Guwahati, India.

Raju Kumar Dewry (RK)

Division of Animal and Fisheries Science, Indian Council of Agricultural Research (ICAR) Research Complex for North Eastern Hill Region, Meghalaya, India.

Manoj Kumar Kalita (MK)

College of Veterinary Science, Assam Agricultural University, Guwahati, India.

Himsikha Chakravarty (H)

Division of Animal and Fisheries Science, Indian Council of Agricultural Research (ICAR) Research Complex for North Eastern Hill Region, Meghalaya, India.

Sourabh Deori (S)

Division of Animal and Fisheries Science, Indian Council of Agricultural Research (ICAR) Research Complex for North Eastern Hill Region, Meghalaya, India. Electronic address: sourabhd1@rediffmail.com.

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