Research Article
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Effects of Borage Oil on Oxidative Damage, Inflammatory Response (IL-6, IL-1β, and TNF- α), and Signaling Pathways (Bax/Bcl-2 and Caspase-3) in Lead Acetate–Induced Nephrotoxicity

Year 2026, Volume: 6 Issue: 1, 10 - 17, 16.03.2026
https://doi.org/10.62425/pharmata.1868902
https://izlik.org/JA96BU27NW

Abstract

Objective: In this study, the potential protective effects of borage oil (BO), a plant-derived oil of medical and nutritional importance, against lead acetate–induced nephrotoxicity were investigated. Methods: In the experimental model, biochemical alterations related to oxidative stress and the antioxidant defence system in rat kidney tissue were evaluated. A total of 30 Sprague Dawley rats were randomly assigned to five experimental groups. Nephrotoxicity was induced by intraperitoneal administration of lead acetate at a dose of 20 mg/kg for 7 days. Borage seed oil was administered orally at doses of 50 and 100 mg/kg for 14 days. Malondialdehyde (MDA) levels, a marker of lipid peroxidation in kidney tissue, were determined using ELISA, while the expression levels of SOD, CAT, and GPx, as well as the gene expression levels of Bax, Bcl-2, and caspase-3, were analysed by RT-PCR. In addition, protein expression levels of inflammatory markers associated with the inflammatory response, including IL-6, IL-1β, and TNF-α, were evaluated by Western blot analysis. Results: The results demonstrated that lead acetate increased oxidative stress in kidney tissue, whereas borage oil enhanced antioxidant defense mechanisms and reduced lipid peroxidation. Lead exposure increased the expression of apoptotic markers (Bax and caspase-3) and decreased Bcl-2 expression in renal tissue, while borage oil—particularly at the 100 mg/kg dose—significantly reversed these alterations and markedly suppressed apoptosis. Furthermore, lead exposure significantly increased the expression of pro-inflammatory markers in kidney tissue, whereas borage oil attenuated this increase, particularly for TNF-α and IL-1β (and IL-6 at the higher dose), thereby modulating the lead-induced inflammatory response. Conclusion: Borage oil exhibited a protective effect against lead acetate–induced renal injury and may alleviate nephrotoxicity.

Ethical Statement

All experimental procedures involving animals were approved by the Atatürk University Local Ethics Committee for Animal Experiments (approval date: 14 March 2025; decision no: 2025/3; protocol no: 62; approval no: E-75296309-050.01.04-2500096596) and were conducted in accordance with the relevant ethical guidelines for animal research.

Supporting Institution

The authors declare that no financial support was received from any individual, institution, or organization for the conduct of this study.

Thanks

The authors would like to thank Atatürk University for providing the necessary infrastructure and technical facilities during the experimental process.

References

  • 1. Algandaby MM. Abatement by Alhagi maurorum of lead-induced nephrotoxicity in rats: emphasis on Nrf2/HO-1. Futur J Pharm Sci. 2025;11(1):9.
  • 2. Sani AH, Amanabo M. Lead: A concise review of its toxicity, mechanism and health effect. GSC Biol Pharm Sci. 2021;15(1):55-62.
  • 3. Ara A, Usmani JA. Lead toxicity: a review. Interdiscip Toxicol. 2015;8(2):55.
  • 4. Mansour LAH, Elshopakey GE, Abdelhamid FM, et al. Hepatoprotective and neuroprotective effects of naringenin against lead-induced oxidative stress, inflammation, and apoptosis in rats. Biomedicines 2023;11(4):1080.
  • 5. Albarakati AJA, Baty RS, Aljoudi AM, et al. Luteolin protects against lead acetate-induced nephrotoxicity through antioxidant, anti-inflammatory, anti-apoptotic, and Nrf2/HO-1 signaling pathways. Mol Biol Rep. 2020;47(4):2591-2603.
  • 6. Abdel-Daim MM, Alkahtani S, Almeer R, Albasher G. Alleviation of lead acetate-induced nephrotoxicity by Moringa oleifera extract in rats: highlighting the antioxidant, anti-inflammatory, and anti-apoptotic activities. Environ Sci Pollut Res. 2020;27(27):33723-33731.
  • 7. Oyagbemi AA, Omobowale TO, Akinrinde AS, Saba AB, Ogunpolu BS, Daramola O. Lack of reversal of oxidative damage in renal tissues of lead acetate‐treated rats. Environ Toxico. 2015;30(11):1235-1243.
  • 8. Wang J, Zhu H, Yang Z, Liu Z. Antioxidative effects of hesperetin against lead acetate-induced oxidative stress in rats. Indian J Pharmacol. 2013;45(4):395-398.
  • 9. Bhattacharjee A, Kulkarni VH, Chakraborty M, Happu PV, Ray A. Ellagic acid restored lead-induced nephrotoxicity by anti-inflammatory, anti-apoptotic and free radical scavenging activities. Heliyon. 2021;7(1).
  • 10. Karaarslan T, Alat O, Can I, et al. Protocatechuic acid mitigates diazinon-induced lung injury in rats through modulation of oxidative stress, inflammatory, Keap-1/Nrf-2/HO-1 and ER stress-mediated apoptotic pathways. Iran J Basic Med Sci. 2026;29(2), 261.
  • 11. Bozkurt I, Halici Z, Zirh EB, Palabiyik-Yucelik SS. EGCG alleviates Ochratoxin A-induced pyroptosis in rat’s kidney by inhibiting NLRP3/Caspase-1/GSDMD signaling pathway. Food Chemical Toxicol. 2024;193:115006.
  • 12. Gurer H, Ercal N. Can antioxidants be beneficial in the treatment of lead poisoning? Free Radic Biol Med. 2000;29(10):927-945.
  • 13. Berköz M, Yiğit A, Krośniak M. Protective role of myricetin and fisetin against nephrotoxicity caused by lead acetate exposure through Up-regulation of Nrf2/HO-1 signalling pathway. Biol Trace Elem Res. 2024;202(9):4032-4046.
  • 14. Bruneton J. Pharmacognosy: Phytochemistry, Medicinal Plants. Editions Médicales; 1999.
  • 15. Duke JA. Handbook of medicinal herbs. CRC press. Preprint posted online 2002.
  • 16. Fan YY, Chapkin RS. Importance of dietary γ-linolenic acid in human health and nutrition. J Nutr. 1998;128(9):1411-1414.
  • 17. Asadi-Samani M, Bahmani M, Rafieian-Kopaei M. The chemical composition, botanical characteristic and biological activities of Borago officinalis: a review. Asian Pac J Trop Med. 2014;7:22-28.
  • 18. Michalak M, Zagórska-Dziok M, Klimek-Szczykutowicz M, Szopa A. Phenolic profile and comparison of the antioxidant, anti-ageing, anti-inflammatory, and protective activities of Borago officinalis extracts on skin cells. Mols. 2023;28(2):868.
  • 19. Bolat M, Bolat İ, Tekin S, Çelebi F. The Effect of Borage Oil (Borago officinalis) on Lead Acetate-Induced Cardiotoxicity. Van Vet J. 2025;36(3):254-260.
  • 20. Tasset-Cuevas I, Fernández-Bedmar Z, Lozano-Baena MD, et al. Protective effect of borage seed oil and gamma linolenic acid on DNA: in vivo and in vitro studies. PLoS One. 2013;8(2):e56986.
  • 21. Michalak M, Zagórska-Dziok M, Klimek-Szczykutowicz M, Szopa A. Phenolic profile and comparison of the antioxidant, anti-ageing, anti-inflammatory, and protective activities of Borago officinalis extracts on skin cells. Mols. 2023;28(2):868.
  • 22. Tekin S, Aykurt F, Çınar B, et al. Investigation of the Effect of Borago officinalis on Bax/Bcl-2/Caspase-3 Pathways Against Spleen Toxicity Induced by Lead Acetate in Rats. Van Vet J. 2025;36(2):132-138.
  • 23. Yousef AOS, Fahad AA, Abdel Moneim AE, Metwally DM, El-Khadragy MF, Kassab RB. The neuroprotective role of coenzyme Q10 against lead acetate-induced neurotoxicity is mediated by antioxidant, anti-inflammatory and anti-apoptotic activities. Int J Environ Res Public Health. 2019;16(16):2895.
  • 24. Abdel Moneim AE, Dkhil MA, Al-Quraishy S. Effects of flaxseed oil on lead acetate-induced neurotoxicity in rats. Biol Trace Elem Res. 2011;144(1):904-913.
  • 25. Ghahremanitamadon F, Shahidi S, Zargooshnia S, Nikkhah A, Ranjbar A, Soleimani Asl, S. Protective effects of Borago officinalis extract on amyloid β‐peptide (25–35)‐induced memory impairment in male rats: A behavioral study. Biomed Res Int. 2014;2014(1):798535.
  • 26. Komaki A, Rasouli B, Shahidi S. Anxiolytic effect of Borago officinalis (Boraginaceae) extract in male rats. Avicenna Journal of Neuro Psycho Physiology. 2015;2(1):34-38.
  • 27. Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95(2):351-358.
  • 28. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. Methods. 2001;25(4):402-408.
  • 29. Dogan T, Onay E, Yildirim BA. Investigation of the effect of Polygonum cognatum Meissn. ethanol extract Bax, Caspase-3, Bcl-2, NF-κB and NRF-2/HO-1 pathways in streptozotocin induced diabetic rats. Diabetes. 2023;5(7):8.
  • 30. Shafiekhani M, Ommati MM, Azarpira N, Heidari R, Salarian AA. Glycine supplementation mitigates lead-induced renal injury in mice. J Exp Pharmacol. Published online 2019:15-22. [
  • 31. Sudjarwo SA, Eraiko K, Sudjarwo GW. Protective effects of piperine on lead acetate induced-nephrotoxicity in rats. Iran J Basic Med Sci. 2017;20(11):1227.
  • 32. Ansar S, Farhat S, Albati AA, Abudawood M, Hamed S. Effect of curcumin and curcumin nanoparticles against lead induced nephrotoxicity. Biomed Res. 2019;30(1):57-60.
  • 33. Li N, Wen L, Yu Z, et al. Effects of folic acid on oxidative damage of kidney in lead-exposed rats. Front Nutr. 2022;9:1035162.
  • 34. Dahran N, Alobaidy MA, Owaydhah WH, et al. Polydatin Mitigates Lead-Induced Nephropathy by Modulating Oxidative Stress, Inflammation, and the AMPK/AKT/Nrf2 Pathway in Rats. Biol Trace Elem Res. 203(10), 5299-5311..
  • 35. Shi Y, Tian C, Yu X, et al. Protective effects of Smilax glabra Roxb. against lead-induced renal oxidative stress, inflammation and apoptosis in weaning rats and HEK-293 cells. Front Pharmacol. 2020;11:556248.
  • 36. Yuan G, Dai S, Yin Z, et al. Sub-chronic lead and cadmium co-induce apoptosis protein expression in liver and kidney of rats. Int J Clin Exp Pathol. 2014;7(6):2905.
  • 37. Saleh SR, Agwah RG, Elblehi SS, Ghareeb AZ, Ghareeb DA, Maher AM. Combination of 10-hydroxy-decanoic acid and ZnO nanoparticles abrogates lead acetate-induced nephrotoxicity in rats: targeting oxidative stress and inflammatory signalling. BMC Pharmacol Toxicol. 2025;26(1):69.
  • 38. Ahmed MB, Ahmed MI, Meki AR, Abdraboh N. Neurotoxic effect of lead on rats: Relationship to Apoptosis. Int J Health Sci (Qassim). 2013;7(2):192.

KURŞUN ASETAT İLE İNDÜKLENEN NEFROTOKSİSİTEDE HODAN YAĞININ OKSİDATİF HASAR, İNFLAMATUVAR YANIT (IL-6, IL-1β ve TNF-α) VE SİNYAL YOLAKLARI (Bax/Bcl-2 ve Kaspaz-3) ÜZERİNE ETKİLERİ

Year 2026, Volume: 6 Issue: 1, 10 - 17, 16.03.2026
https://doi.org/10.62425/pharmata.1868902
https://izlik.org/JA96BU27NW

Abstract

Amaç: Bu çalışmada, tıbbi ve besinsel açıdan önemli bir bitkisel yağ olan hodan yağının (BO), kurşun asetat ile oluşturulan nefrotoksisiteye karşı olası koruyucu etkileri araştırılmıştır. Yöntem: Deneysel modelde, sıçan böbrek dokusunda oksidatif stres ve antioksidan savunma sistemi ile ilişkili biyokimyasal değişiklikler değerlendirilmiştir. Toplam 30 adet Sprague Dawley sıçanı rastgele seçilerek beş deney grubuna ayrılmıştır. Nefrotoksisite modeli, sıçanlara 7 gün süreyle intraperitoneal yoldan 20 mg/kg dozunda kurşun asetat uygulanarak oluşturulmuştur. Hodan tohumu yağı ise 14 gün boyunca oral yolla 50 ve 100 mg/kg dozlarında verilmiştir. Böbrek dokusunda lipid peroksidasyonunun göstergesi olan MDA düzeyleri ELISA yöntemiyle belirlenirken SOD, CAT ve GPx ekspresyon düzeyleri ile Bax, Bcl-2 ve kaspaz-3 gen ekspresyonları RT-PCR yöntemi kullanılarak analiz edilmiştir. Ayrıca inflamatuar yanıtla ilişkili IL-6, IL-1β ve TNF-α protein ekspresyonları Western blot yöntemiyle değerlendirilmiştir. Bulgular: Elde edilen bulgular, Kurşun asetat böbrek dokusunda oksidatif stresi artırırken, hodan yağı antioksidan savunmayı güçlendirerek lipid peroksidasyonunu azaltmıştır. Pb maruziyeti böbrek dokusunda apoptotik belirteçleri (Bax ve Kaspaz-3) artırıp Bcl-2 ekspresyonunu azaltırken, hodan yağı özellikle 100 mg/kg dozda bu değişimleri tersine çevirerek apoptozu anlamlı biçimde baskılamıştır. Pb maruziyeti böbrek dokusunda proinflamatuvar belirteçlerin ekspresyonunu anlamlı düzeyde artırırken, hodan yağı özellikle TNF-α ve IL-1β’de (ve yüksek dozda IL-6’da) bu artışı baskılayarak Pb ile indüklenen inflamatuvar yanıtı modüle etmiştir. Sonuç: Hodan yağının kurşun asetata bağlı böbrek hasarına karşı koruyucu etki gösterdiği ve nefrotoksisiteyi hafifletebileceği kanaatine varılmıştır.

Ethical Statement

Bu çalışmada hayvanlar üzerinde gerçekleştirilen tüm deneysel prosedürler, Atatürk Üniversitesi Hayvan Deneyleri Yerel Etik Kurulu tarafından onaylanmıştır (onay tarihi: 14.03.2025; karar no: 2025/3; protokol no: 62; onay no: E-75296309-050.01.04-2500096596) ve hayvan deneyleriyle ilgili etik ilke ve yönergelere uygun olarak yürütülmüştür.

Supporting Institution

Yazarlar, bu çalışmanın gerçekleştirilmesi sırasında herhangi bir kişi, kurum veya kuruluştan finansal destek alınmadığını beyan eder.

Thanks

Yazarlar, deneysel sürecin yürütülmesinde sağlanan altyapı ve teknik olanaklar için Atatürk Üniversitesi’ne teşekkür eder.

References

  • 1. Algandaby MM. Abatement by Alhagi maurorum of lead-induced nephrotoxicity in rats: emphasis on Nrf2/HO-1. Futur J Pharm Sci. 2025;11(1):9.
  • 2. Sani AH, Amanabo M. Lead: A concise review of its toxicity, mechanism and health effect. GSC Biol Pharm Sci. 2021;15(1):55-62.
  • 3. Ara A, Usmani JA. Lead toxicity: a review. Interdiscip Toxicol. 2015;8(2):55.
  • 4. Mansour LAH, Elshopakey GE, Abdelhamid FM, et al. Hepatoprotective and neuroprotective effects of naringenin against lead-induced oxidative stress, inflammation, and apoptosis in rats. Biomedicines 2023;11(4):1080.
  • 5. Albarakati AJA, Baty RS, Aljoudi AM, et al. Luteolin protects against lead acetate-induced nephrotoxicity through antioxidant, anti-inflammatory, anti-apoptotic, and Nrf2/HO-1 signaling pathways. Mol Biol Rep. 2020;47(4):2591-2603.
  • 6. Abdel-Daim MM, Alkahtani S, Almeer R, Albasher G. Alleviation of lead acetate-induced nephrotoxicity by Moringa oleifera extract in rats: highlighting the antioxidant, anti-inflammatory, and anti-apoptotic activities. Environ Sci Pollut Res. 2020;27(27):33723-33731.
  • 7. Oyagbemi AA, Omobowale TO, Akinrinde AS, Saba AB, Ogunpolu BS, Daramola O. Lack of reversal of oxidative damage in renal tissues of lead acetate‐treated rats. Environ Toxico. 2015;30(11):1235-1243.
  • 8. Wang J, Zhu H, Yang Z, Liu Z. Antioxidative effects of hesperetin against lead acetate-induced oxidative stress in rats. Indian J Pharmacol. 2013;45(4):395-398.
  • 9. Bhattacharjee A, Kulkarni VH, Chakraborty M, Happu PV, Ray A. Ellagic acid restored lead-induced nephrotoxicity by anti-inflammatory, anti-apoptotic and free radical scavenging activities. Heliyon. 2021;7(1).
  • 10. Karaarslan T, Alat O, Can I, et al. Protocatechuic acid mitigates diazinon-induced lung injury in rats through modulation of oxidative stress, inflammatory, Keap-1/Nrf-2/HO-1 and ER stress-mediated apoptotic pathways. Iran J Basic Med Sci. 2026;29(2), 261.
  • 11. Bozkurt I, Halici Z, Zirh EB, Palabiyik-Yucelik SS. EGCG alleviates Ochratoxin A-induced pyroptosis in rat’s kidney by inhibiting NLRP3/Caspase-1/GSDMD signaling pathway. Food Chemical Toxicol. 2024;193:115006.
  • 12. Gurer H, Ercal N. Can antioxidants be beneficial in the treatment of lead poisoning? Free Radic Biol Med. 2000;29(10):927-945.
  • 13. Berköz M, Yiğit A, Krośniak M. Protective role of myricetin and fisetin against nephrotoxicity caused by lead acetate exposure through Up-regulation of Nrf2/HO-1 signalling pathway. Biol Trace Elem Res. 2024;202(9):4032-4046.
  • 14. Bruneton J. Pharmacognosy: Phytochemistry, Medicinal Plants. Editions Médicales; 1999.
  • 15. Duke JA. Handbook of medicinal herbs. CRC press. Preprint posted online 2002.
  • 16. Fan YY, Chapkin RS. Importance of dietary γ-linolenic acid in human health and nutrition. J Nutr. 1998;128(9):1411-1414.
  • 17. Asadi-Samani M, Bahmani M, Rafieian-Kopaei M. The chemical composition, botanical characteristic and biological activities of Borago officinalis: a review. Asian Pac J Trop Med. 2014;7:22-28.
  • 18. Michalak M, Zagórska-Dziok M, Klimek-Szczykutowicz M, Szopa A. Phenolic profile and comparison of the antioxidant, anti-ageing, anti-inflammatory, and protective activities of Borago officinalis extracts on skin cells. Mols. 2023;28(2):868.
  • 19. Bolat M, Bolat İ, Tekin S, Çelebi F. The Effect of Borage Oil (Borago officinalis) on Lead Acetate-Induced Cardiotoxicity. Van Vet J. 2025;36(3):254-260.
  • 20. Tasset-Cuevas I, Fernández-Bedmar Z, Lozano-Baena MD, et al. Protective effect of borage seed oil and gamma linolenic acid on DNA: in vivo and in vitro studies. PLoS One. 2013;8(2):e56986.
  • 21. Michalak M, Zagórska-Dziok M, Klimek-Szczykutowicz M, Szopa A. Phenolic profile and comparison of the antioxidant, anti-ageing, anti-inflammatory, and protective activities of Borago officinalis extracts on skin cells. Mols. 2023;28(2):868.
  • 22. Tekin S, Aykurt F, Çınar B, et al. Investigation of the Effect of Borago officinalis on Bax/Bcl-2/Caspase-3 Pathways Against Spleen Toxicity Induced by Lead Acetate in Rats. Van Vet J. 2025;36(2):132-138.
  • 23. Yousef AOS, Fahad AA, Abdel Moneim AE, Metwally DM, El-Khadragy MF, Kassab RB. The neuroprotective role of coenzyme Q10 against lead acetate-induced neurotoxicity is mediated by antioxidant, anti-inflammatory and anti-apoptotic activities. Int J Environ Res Public Health. 2019;16(16):2895.
  • 24. Abdel Moneim AE, Dkhil MA, Al-Quraishy S. Effects of flaxseed oil on lead acetate-induced neurotoxicity in rats. Biol Trace Elem Res. 2011;144(1):904-913.
  • 25. Ghahremanitamadon F, Shahidi S, Zargooshnia S, Nikkhah A, Ranjbar A, Soleimani Asl, S. Protective effects of Borago officinalis extract on amyloid β‐peptide (25–35)‐induced memory impairment in male rats: A behavioral study. Biomed Res Int. 2014;2014(1):798535.
  • 26. Komaki A, Rasouli B, Shahidi S. Anxiolytic effect of Borago officinalis (Boraginaceae) extract in male rats. Avicenna Journal of Neuro Psycho Physiology. 2015;2(1):34-38.
  • 27. Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95(2):351-358.
  • 28. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. Methods. 2001;25(4):402-408.
  • 29. Dogan T, Onay E, Yildirim BA. Investigation of the effect of Polygonum cognatum Meissn. ethanol extract Bax, Caspase-3, Bcl-2, NF-κB and NRF-2/HO-1 pathways in streptozotocin induced diabetic rats. Diabetes. 2023;5(7):8.
  • 30. Shafiekhani M, Ommati MM, Azarpira N, Heidari R, Salarian AA. Glycine supplementation mitigates lead-induced renal injury in mice. J Exp Pharmacol. Published online 2019:15-22. [
  • 31. Sudjarwo SA, Eraiko K, Sudjarwo GW. Protective effects of piperine on lead acetate induced-nephrotoxicity in rats. Iran J Basic Med Sci. 2017;20(11):1227.
  • 32. Ansar S, Farhat S, Albati AA, Abudawood M, Hamed S. Effect of curcumin and curcumin nanoparticles against lead induced nephrotoxicity. Biomed Res. 2019;30(1):57-60.
  • 33. Li N, Wen L, Yu Z, et al. Effects of folic acid on oxidative damage of kidney in lead-exposed rats. Front Nutr. 2022;9:1035162.
  • 34. Dahran N, Alobaidy MA, Owaydhah WH, et al. Polydatin Mitigates Lead-Induced Nephropathy by Modulating Oxidative Stress, Inflammation, and the AMPK/AKT/Nrf2 Pathway in Rats. Biol Trace Elem Res. 203(10), 5299-5311..
  • 35. Shi Y, Tian C, Yu X, et al. Protective effects of Smilax glabra Roxb. against lead-induced renal oxidative stress, inflammation and apoptosis in weaning rats and HEK-293 cells. Front Pharmacol. 2020;11:556248.
  • 36. Yuan G, Dai S, Yin Z, et al. Sub-chronic lead and cadmium co-induce apoptosis protein expression in liver and kidney of rats. Int J Clin Exp Pathol. 2014;7(6):2905.
  • 37. Saleh SR, Agwah RG, Elblehi SS, Ghareeb AZ, Ghareeb DA, Maher AM. Combination of 10-hydroxy-decanoic acid and ZnO nanoparticles abrogates lead acetate-induced nephrotoxicity in rats: targeting oxidative stress and inflammatory signalling. BMC Pharmacol Toxicol. 2025;26(1):69.
  • 38. Ahmed MB, Ahmed MI, Meki AR, Abdraboh N. Neurotoxic effect of lead on rats: Relationship to Apoptosis. Int J Health Sci (Qassim). 2013;7(2):192.
There are 38 citations in total.

Details

Primary Language English
Subjects Biochemistry and Cell Biology (Other)
Journal Section Research Article
Authors

İlyas Bozkurt 0000-0003-1830-3416

Mesut Bünyami Halıcı 0000-0002-7473-2955

Submission Date January 21, 2026
Acceptance Date March 3, 2026
Publication Date March 16, 2026
DOI https://doi.org/10.62425/pharmata.1868902
IZ https://izlik.org/JA96BU27NW
Published in Issue Year 2026 Volume: 6 Issue: 1

Cite

EndNote Bozkurt İ, Halıcı MB (March 1, 2026) Effects of Borage Oil on Oxidative Damage, Inflammatory Response (IL-6, IL-1β, and TNF- α), and Signaling Pathways (Bax/Bcl-2 and Caspase-3) in Lead Acetate–Induced Nephrotoxicity. Pharmata 6 1 10–17.

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