# Dietary Lycopene Mitigates Reproductive Impairment in Heat-Stressed Rongchang Boars: Roles of Antioxidant, Anti-Inflammatory and Nrf2 Pathway

**Authors:** Ying Lei, Hanxin Liu, Qiujin Xiang, Ying Liu, De Wu, Junjie Zhang, Yan Lin

PMC · DOI: 10.3390/antiox15020245 · Antioxidants · 2026-02-13

## TL;DR

Adding lycopene to the diet of heat-stressed Rongchang boars improves sperm quality and reduces tissue damage by reducing oxidative stress and inflammation.

## Contribution

This study identifies the testis and cauda epididymis as key tissues where lycopene mitigates heat stress through the Nrf2 pathway.

## Key findings

- Heat stress increased sperm abnormalities and oxidative stress in multiple tissues, with the testis and cauda epididymis most affected.
- Lycopene supplementation improved sperm motility, reduced inflammation, and upregulated Nrf2 pathway genes in heat-stressed boars.
- Lycopene's protective effects are linked to its regulation of the Nrf2 antioxidant signaling pathway and reduction of inflammatory markers.

## Abstract

Heat stress (HS) severely impairs boar reproductive function by inducing oxidative stress and inflammatory responses, while lycopene (LYC), as a potent antioxidant, exerts a potential protective effect on the male reproductive system. This study aimed to clarify the mechanism underlying LYC-mediated alleviation of HS-induced decline in semen quality in Rongchang boars, identify the most affected tissues, and explore its regulatory role in the Nrf2 (Nuclear factor E2-related factor 2) pathway. A total of 18 Rongchang boars with an initial body weight of 15.81 ± 1.07 kg were randomly assigned to three groups (6 boars per group): the control group (CON, 26 ± 1 °C), the heat stress group (HS, exposed to 35 ± 1 °C for 8 h daily), and the heat stress + 100 mg/kg lycopene group (HS + LYC). After 28 days of adaptive feeding and 14 days of HS treatment, samples were collected for semen quality analysis, testicular histological analysis, antioxidant index detection, transcriptome analysis, Nrf2 pathway detection, and inflammatory index detection. The results showed that HS significantly increased the sperm abnormality rate (p < 0.05), damaged the testicular structure, and induced oxidative stress in serum, lung, liver, left ventricle, testis, and epididymis (caput epididymis, corpus epididymis, cauda epididymis), with varying degrees of oxidative stress observed in these samples. Among these tissues, the testis and cauda epididymis exhibited the most significant responses to HS and LYC, with the comprehensive impact magnitudes of 317% and 514%, respectively. Enrichment analysis of differentially expressed genes (DEGs) in these two tissues revealed that the pathways mediating oxidative stress response displayed distinct tissue specificity, and all of them were closely associated with the Nrf2 antioxidant signaling pathway. HS significantly downregulated the mRNA expressions of Nrf2, Quinone Oxidoreductase (NQO1), Heme Oxygenase 1 (HMOX1) and Glutamate-Cysteine Ligase Catalytic Subunit (GCLC) genes as well as the protein level of Nrf2 in the testis and cauda epididymis, increased the protein level of Keap1, and significantly elevated the levels of interleukin-6 (IL-6), interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α) in these two tissues (p < 0.05). Compared with the HS group, dietary supplementation of LYC significantly improved sperm motility and the proportion of rapidly progressive sperm, reduced the proportion of immotile sperm and sperm abnormality rate (p < 0.05), alleviated testicular damage and oxidative stress in various tissues, upregulated the mRNA expressions of Nrf2 and HMOX1 genes in the testis as well as the mRNA expressions of Nrf2, NQO1, HMOX1 and GCLC genes in cauda epididymis (p < 0.05), significantly increased the Nrf2 protein level and decreased the Keap1 protein level in these two tissues, and simultaneously decreased the levels of the aforementioned inflammatory factors (p < 0.05). In conclusion, dietary supplementation with 100 mg/kg LYC can alleviate HS-induced decline in semen quality and testicular damage by regulating the oxidative status and inflammatory level of relevant tissues (e.g., testis and cauda epididymis) in boars, and this protective effect may be associated with the regulation of the Nrf2 signaling pathway.

## Linked entities

- **Genes:** GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551], NQO1 (NAD(P)H quinone dehydrogenase 1) [NCBI Gene 1728], HMOX1 (heme oxygenase 1) [NCBI Gene 3162], GCLC (glutamate-cysteine ligase catalytic subunit) [NCBI Gene 2729], KEAP1 (kelch like ECH associated protein 1) [NCBI Gene 9817], IL6 (interleukin 6) [NCBI Gene 3569], IL1B (interleukin 1 beta) [NCBI Gene 3553], TNF (tumor necrosis factor) [NCBI Gene 7124]
- **Proteins:** GABPA (GA binding protein transcription factor subunit alpha), KEAP1 (kelch like ECH associated protein 1)
- **Chemicals:** lycopene (PubChem CID 446925)

## Full-text entities

- **Genes:** Cat (catalase) [NCBI Gene 24248] {aka CS1, Cas1, Cat01, Catl, Cs-1}, RAD54B (RAD54 homolog B) [NCBI Gene 100513148], GCLM (glutamate-cysteine ligase modifier subunit) [NCBI Gene 2730] {aka GLCLR}, GSTO2 (glutathione S-transferase omega 2) [NCBI Gene 100152209], IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, CRYZ (crystallin zeta) [NCBI Gene 1429], CHAC1 (ChaC glutathione specific gamma-glutamylcyclotransferase 1) [NCBI Gene 100524723], CAT (catalase) [NCBI Gene 397568], HMOX1 (heme oxygenase 1) [NCBI Gene 445512] {aka HSP32}, JAK1 (Janus kinase 1) [NCBI Gene 397202], Nlrp3 (NLR family, pyrin domain containing 3) [NCBI Gene 287362] {aka Cias1}, Nfe2l2 (nuclear factor, erythroid derived 2, like 2) [NCBI Gene 18024] {aka Nrf2}, Il1b (interleukin 1 beta) [NCBI Gene 24494] {aka IL-1F2}, Nqo1 (NAD(P)H dehydrogenase, quinone 1) [NCBI Gene 18104] {aka Dia4, Dtd, Nmo-1, Nmo1, Nmor1, Ox-1}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, NQO1 (NAD(P)H quinone dehydrogenase 1) [NCBI Gene 1728] {aka DHQU, DIA4, DTD, NMOR1, NMORI, QR1}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 100126861] {aka Akt, PKB}, Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, ATM (ATM serine/threonine kinase) [NCBI Gene 100101922], Il18 (interleukin 18) [NCBI Gene 29197] {aka IL-1 gamma, IL-18}, KEAP1 (kelch like ECH associated protein 1) [NCBI Gene 100136900] {aka INRF2}, MAPK13 (mitogen-activated protein kinase 13) [NCBI Gene 100155841], ATP6 (ATP synthase F0 subunit 6) [NCBI Gene 808506], IL1B (interleukin 1 beta) [NCBI Gene 397122] {aka IL1B1}, GCLC (glutamate-cysteine ligase catalytic subunit) [NCBI Gene 2729] {aka CNSHA7, GCL, GCS, GLCL, GLCLC}, ND1 (NADH dehydrogenase subunit 1) [NCBI Gene 808501], COX1 (cytochrome c oxidase subunit I) [NCBI Gene 808503], JUN (Jun proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 396913] {aka C-JUN}, UCP2 (uncoupling protein 2) [NCBI Gene 397549] {aka SLC25A8}, Interleukin-6 [NCBI Gene 100628202], GPX7 (glutathione peroxidase 7) [NCBI Gene 100621417], GPX5 (glutathione peroxidase 5) [NCBI Gene 396920], SOD3 (superoxide dismutase 3) [NCBI Gene 780439], NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, GCLC (glutamate-cysteine ligase catalytic subunit) [NCBI Gene 100522018], beta-actin [NCBI Gene 100158242], NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 100516343], IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, KEAP1 (kelch like ECH associated protein 1) [NCBI Gene 9817] {aka INrf2, KLHL19}, GPX6 (glutathione peroxidase 6) [NCBI Gene 100154091], CRYZ (crystallin zeta) [NCBI Gene 733653], AOX1 (aldehyde oxidase 1) [NCBI Gene 100523701], LOC396797 (beta actin) [NCBI Gene 396797], CYTB (cytochrome b) [NCBI Gene 808513], TNF (tumor necrosis factor) [NCBI Gene 397086] {aka TNFSF2, TNFa}, HMOX1 (heme oxygenase 1) [NCBI Gene 3162] {aka HMOX1D, HO-1, HSP32, bK286B10}, MAPK10 (mitogen-activated protein kinase 10) [NCBI Gene 100521736], PIK3R6 (phosphoinositide-3-kinase regulatory subunit 6) [NCBI Gene 100034246], SRXN1 (sulfiredoxin 1) [NCBI Gene 140809] {aka C20orf139, Npn3, SRX, SRX1}, TXNRD1 (thioredoxin reductase 1) [NCBI Gene 7296] {aka GRIM-12, TR, TR1, TRXR1, TXNR, TXNR1}
- **Diseases:** inflammatory damage (MESH:D018746), sperm abnormalities (MESH:C567467), Inflammatory (MESH:D007249), injury to (MESH:D014947), morphological abnormalities (MESH:D000013), testicular (MESH:D013733), respiratory diseases (MESH:D012140), Reproductive Impairment (MESH:D060737), HS (MESH:D018882), non (MESH:C580335), cardiovascular disease (MESH:D002318), tissue (MESH:D017695), communicable diseases (MESH:D003141)
- **Chemicals:** MDA (MESH:D015104), nitrogen (MESH:D009584), wax (MESH:D014885), ginsenoside Rg3 (MESH:C097367), Paraffin (MESH:D010232), T (MESH:D014316), Zn (MESH:D015032), RSV (MESH:D000077185), D-biotin (MESH:D001710), Cu (MESH:D003300), water (MESH:D014867), LYC (MESH:D000077276), carotenoid (MESH:D002338), nicotinamide (MESH:D009536), Fe (MESH:D007501), bisphenol A (MESH:C006780), Se (MESH:D012643), Malondialdehyde (MESH:D008315), DBP (MESH:D003993), balsam (MESH:D001453), superoxide (MESH:D013481), AOC (-), H&amp;E (MESH:D006371), Crystal Violet (MESH:D005840), ZEA (MESH:D015025), hematoxylin (MESH:D006416), eosin (MESH:D004801), Mn (MESH:D008345), folic acid (MESH:D005492), ROS (MESH:D017382), D-pantothenic acid (MESH:D010205), GSH (MESH:D005978), lipid (MESH:D008055), paraformaldehyde (MESH:C003043), astaxanthin (MESH:C005948), I (MESH:D007455)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Sus scrofa domesticus (domestic pig, subspecies) [taxon 9825], Sus scrofa (pig, species) [taxon 9823], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Suidae (boars, family) [taxon 9821], Capra hircus (domestic goat, species) [taxon 9925]
- **Cell lines:** ARPE-19 — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0145), IPEC-J2 — Sus scrofa (Pig), Spontaneously immortalized cell line (CVCL_2246)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938134/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938134/full.md

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Source: https://tomesphere.com/paper/PMC12938134