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The Effect of Borage Oil (Borago officinalis) on Lead Acetate-Induced Cardiotoxicity

Year 2025, Volume: 36 Issue: 3, 254 - 260, 30.11.2025
https://doi.org/10.36483/vanvetj.1774021

Abstract

Lead acetate (PbAc) is an environmental toxin known to induce cardiotoxicity via oxidative stress, inflammation, and apoptosis. This study examined the protective role of borage oil (BO) in PbAc-exposed rats. Five groups were studied: Control, PbAc, PbAc + BO-50, PbAc + BO-100, and BO. Oxidative stress markers (malondialdehyde (MDA), glutathione (GSH), superoxide dismutase (SOD) and catalase (CAT)), inflammatory cytokines (tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β), interleukin-6 (IL-6), and nuclear factor kappa B (NF-κB)), and apoptotic genes (B-cell lymphoma 2 (Bcl-2), Bcl-2-associated X protein (Bax) and Caspase-3) were evaluated using ELISA, real-time PCR, and Western blot. PbAc exposure significantly increased MDA levels (p<0.0001), while BO treatment dose-dependently reduced MDA concentrations (p<0.0001). Antioxidant enzyme activities (SOD, CAT, GSH) were significantly reduced in the PbAc group (p<0.0001) but were restored following BO administration (p<0.0001). Pro-inflammatory cytokines TNF-α, IL-1β, IL-6, and NF-κB were upregulated by PbAc (p<0.0001) and significantly downregulated with BO treatment. Apoptotic gene expression analysis revealed increased levels of Bax and Caspase-3, along with decreased expression of Bcl-2 in the PbAc group (p<0.0001), indicating apoptosis. These changes were reversed by BO, which lowered Bax and caspase-3 while upregulating Bcl-2 (p<0.0001). Western blot results confirmed the decrease in NF-κB protein levels in BO-treated rats (p<0.0001). These findings suggest that borage oil alleviates PbAc-induced cardiac damage by counteracting oxidative stress, suppressing inflammation, and inhibiting apoptosis. Thus, borage oil may offer a promising protective strategy against heavy metal-induced cardiotoxicity. Further research is recommended to support its clinical relevance.

Ethical Statement

This study was approved by the Atatürk University Animal Experiments Local Ethics Committee (2025/04, Decision No: 72).

References

  • Abdelhamid FM, Mahgoub HA, Ateya AI (2020). Ameliorative effect of curcumin against lead acetate–induced hemato-biochemical alterations, hepatotoxicity, and testicular oxidative damage in rats. Environ Sci Pollut Res, 27, 10950-10965.
  • Abdel-Daim MM, Alkahtani S, Almeer R, Albasher G (2020). 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, 27 (27), 33723-33731.
  • Abdel-Emam RA, Ali MF (2022). Effect of L-carnitine supplementation on lead acetate-induced liver cell apoptosis and inflammation: Role of caspase-3 and glycogen synthase kinase-3β enzymes. Life Sci, 291, 120277.
  • Aboutalebi S, Zare N, Sheikhzadeh P (2023). Physio-biochemical response of Borago officinalis L. roots to cadmium toxicity. Russ J Plant Physl, 70 (3), 37.
  • Afkhami-Ardakani M, Hassanzadeh S, Shahrooz R et al. (2017). Phytotherapy and phytopharmacology for reduction of cyclophosphamide-induced toxicity in the male urinary system. J Renal Inj Prev, 6 (3), 164-170.
  • Akhavan N, Parikh K, Salazar G, Arjmandi B (2020). The antioxidative effects of Borago officinalis in lipopolysaccharide and hydrogen peroxide-activated RAW 264.7 macrophages. Curr dev nutr, 4, 045-001.
  • Badary DM (2017). Folic acid protects against lead acetate-induced hepatotoxicity by decreasing NF-κB, IL-1β production and lipid peroxidation mediataed cell injury. Pathophysiology, 24 (1), 39-44.
  • Balakin AA, Minigalieva IA, Kuznetsov DA et al. (2024). Dose dependency of subchronic lead acetate exposure on biophysical characteristics of rats’ right atrium and ventricle. Eur Phys J Spec Top, 233 (23), 3507-3517.
  • Bolat İ, Bolat M, Kiliçlioğlu M et al. (2025a). Differential TLR2 and TLR4 mediated inflammatory and apoptotic responses in asymptomatic and symptomatic Leptospira interrogans infections in canine uterine tissue. Microb Pathog, 198, 107186.
  • Bolat M, Laçin B, Çelebi F (2024). Ratlarda Bisfenol-A’nın Neden Olduğu Nörotoksisite Üzerine Hesperidinin Etkilerinin Araştırılması. Vet sci and pract, 19 (1), 17-24.
  • Bolat M, Tekin S, Bolat İ et al. (2025b). Gallic acid’s protective mechanisms against acrylamide-induced pulmonary injury: in vivo and in silico insights into the Nrf-2/HO-1/NFκB pathway modulation. N-S Arch Pharmacol, 398, 11821–11837.
  • Chen C, Lin B, Qi S et al. (2019). Protective effects of salidroside on lead acetate-induced oxidative stress and hepatotoxicity in Sprague-Dawley rats. Biol Trace Elem Res, 191, 426-434.
  • Dogan T, Yıldırım BA, Kapakin KAT et al. (2025). Protective effects of crocin against gentamicin-induced damage in rat testicular tissue: modulating the levels of NF-κB/TLR-4 and Bax/Bcl-2/Caspase-3 signaling pathways. Food Chem Toxicol, 115407.
  • Din SR, Saeed, S, Khan SU et al. (2023). Bioactive compounds (BACs): A novel approach to treat and prevent cardiovascular diseases. Curr Probl Cardiol, 48 (7), 101664.
  • Feng L, Yang X, Shi Y et al. (2018): Co-exposure subacute toxicity of silica nanoparticles and lead acetate on cardiovascular system. Int J Nanomedicine, 7819-7834.
  • Gilani AH, Bashir S, Khan AU (2007). Pharmacological basis for the use of Borago officinalis in gastrointestinal, respiratory and cardiovascular disorders. J Ethnopharmacol, 114 (3), 393-399.
  • Harshitha P, Bose K, Dsouza HS (2024). Influence of lead-induced toxicity on the inflammatory cytokines. Toxicology, 503, 153771.
  • Ibrahim NM, Eweis EA, El-Beltagi HS, Abdel-Mobdy YE (2012). Effect of lead acetate toxicity on experimental male albino rat. Asian Pac J Trop Biomed, 2 (1), 41-46.
  • Ileriturk M, Benzer F, Aksu EH et al. (2021). Chrysin protects against testicular toxicity caused by lead acetate in rats with its antioxidant, anti‐inflammatory, and antiapoptotic properties. J Food Biochem, 45 (2), e13593.
  • Jasem SA, Abas AK (2022). Physiological Effect of Green Synthesized Silver Nanoparticles Agnps on Albino Rat Testis. Egypt J Hosp Med, 89 (2), 8076-8082.
  • Kmail A (2024) Mitigating digestive disorders: Action mechanisms of Mediterranean herbal active compounds. Open Life Sci,19 (1), 20220857.
  • Khattab HA, Abdallah IZ, Yousef FM, Huwait EA (2017). Efficiency of borage seeds oil against gamma irradiation-induced hepatotoxicity in male rats: possible antioxidant activity. Afr J Tradit Complement Altern Med, 14 (4), 169-179.
  • Li C, Shi L, Peng C et al. (2021). Lead-induced cardiomyocytes apoptosis by inhibiting gap junction intercellular communication via autophagy activation. Chem Biol Interact, 337, 109331.
  • Li Y, Cai W, Ai Z et al. (2023). Protective effects of sinomenine hydrochloride on lead-induced oxidative stress, inflammation, and apoptosis in mouse liver. Environ Sci Pollut Res Int, 30 (3), 7510-7521.
  • Mohammadi M, Rashidizad SA, Lashkari N et al. (2020). Supplement Therapy in Multiple Sclerosis: A Pharmacological View. Avicenna J Pharm Res, 1 (1), 37-45.
  • Oluranti OI, Adeyemo VA, Achile EO et al. (2022). Rutin improves cardiac and erythrocyte membrane–bound ATPase activities in male rats exposed to cadmium chloride and lead acetate. Biol Trace Elem Res, 1-9.
  • Ovie FO, Nwanama EK, Nwafor CC et al. (2023). Nephroprotective effects of Cajanus cajan on lead acetate-induced kidney damage of male Wistar rats. J. Clin. Exp. Med., 20 (2), 50-54.
  • Owumi SE, Otunla MT, Arunsi UO (2023). A biochemical and histology experimental approach to investigate the adverse effect of chronic lead acetate and dietary furan on rat lungs. Biometals, 36 (1), 201-216.
  • Oyem JC, Chris-Ozoko LE, Enaohwo MT et al. (2021). Antioxidative properties of Ocimum gratissimum alters Lead acetate induced oxidative damage in lymphoid tissues and hematological parameters of adult Wistar rats. Toxicol rep, 8, 215-222.
  • Rahman S, Sultana S (2006). Chemopreventive activity of glycyrrhizin on lead acetate mediated hepatic oxidative stress and its hyperproliferative activity in Wistar rats. Chem Biol Interact, 160 (1), 61-69.
  • Riaz T, Akram M, Laila U et al. (2023). Anti-inflammatory activity of medicinal plants and herbs: A review. IAIM 10 (12).
  • Samarghandian S, Borji A, Afshari R et al. (2013). The effect of lead acetate on oxidative stress and antioxidant status in rat bronchoalveolar lavage fluid and lung tissue. Toxicol Mech Methods, 23 (6), 432-436.
  • Şimşek H, Küçükler S, Gür C et al. (2023). Protective effects of sinapic acid against lead acetate-induced nephrotoxicity: a multi-biomarker approach. Environ Sci Pollut Res Int, 30 (45), 101208-101222.
  • Tanwar B, Goyal A, Kumar V et al. (2021). Borage (Borago officinalis) seed. OHFA, 351-371.
  • Torun H, Eroğlu E (2021). Antioxidant defense system in Borago officinalis L. under drought stress. TURKJANS, 8 (4), 1048-1055.
  • Tuncer SÇ, Akarsu SA, Küçükler S et al. (2023). Effects of sinapic acid on lead acetate‐induced oxidative stress, apoptosis and inflammation in testicular tissue. Environ toxicol, 38 (11), 2656-2667.
  • Zhou L, Wang S, Cao L et al. (2021). Lead acetate induces apoptosis in Leydig cells by activating PPARγ/caspase-3/PARP pathway. Int J Environ Health Res, 31 (1), 34-44.

Kurşun Asetat ile İndüklenen Kardiyotoksisite Üzerine Hodan Yağının (Borago officinalis) Koruyucu Etkisi

Year 2025, Volume: 36 Issue: 3, 254 - 260, 30.11.2025
https://doi.org/10.36483/vanvetj.1774021

Abstract

Kurşun asetat (PbAc), oksidatif stres, inflamasyon ve apoptoz yoluyla kardiyotoksisiteye neden olduğu bilinen bir çevresel toksindir. Bu çalışma, PbAc’ye maruz bırakılan sıçanlarda hodan yağının (BO) koruyucu rolünü incelemiştir. Beş grup çalışmaya dahil edilmiştir: Kontrol, PbAc, PbAc + BO-50, PbAc + BO-100 ve BO. Oksidatif stres belirteçleri (malondialdehit (MDA), glutatyon (GSH), süperoksit dismutaz (SOD) ve katalaz (CAT)), inflamatuvar sitokinler (tümör nekroz faktörü-alfa (TNF-α), interlökin-1 beta (IL-1β), interlökin-6 (IL-6) ve nükleer faktör kappa B (NF-κB)) ile apoptotik genler (B hücre lenfoması-2 (Bcl-2), Bcl-2 ilişkili X proteini (Bax) ve Kaspaz-3) ELISA, gerçek zamanlı PCR ve Western blot yöntemleriyle değerlendirildi. PbAc maruziyeti MDA düzeylerini anlamlı olarak artırdı (p<0.0001), BO tedavisi ise doza bağımlı şekilde MDA konsantrasyonlarını azalttı (p<0.0001). Antioksidan enzim aktiviteleri (SOD, CAT, GSH) PbAc grubunda belirgin şekilde azaldı (p<0.0001), ancak BO uygulaması sonrası yeniden düzeldi (p<0.0001). Proinflamatuvar sitokinler TNF-α, IL-1β, IL-6 ve NF-κB, PbAc tarafından yukarı regüle edildi (p<0.0001) ve BO tedavisi ile anlamlı şekilde baskılandı. Apoptotik gen ekspresyon analizleri, PbAc grubunda Bax ve Kaspaz-3 düzeylerinin artığını, Bcl-2 ekspresyonunun ise azaldığını ortaya koydu (p<0.0001), bu da apoptozisi göstermektedir. BO, Bax ve Kaspaz-3’ü azaltırken Bcl-2’yi yukarı regüle ederek bu değişiklikleri tersine çevirdi (p<0.0001). Western blot sonuçları, BO ile tedavi edilen sıçanlarda NF-κB protein düzeylerinde azalmayı doğruladı (p<0.0001). Bu bulgular, hodan yağının PbAc’nin neden olduğu kardiyak hasarı oksidatif stresi dengeleyerek, inflamasyonu baskılayarak ve apoptozu inhibe ederek hafiflettiğini göstermektedir. Dolayısıyla, hodan yağı ağır metal kaynaklı kardiyotoksisiteye karşı umut verici bir koruyucu strateji sunabilir. Klinik önemini desteklemek için ileri çalışmalara ihtiyaç vardır.

References

  • Abdelhamid FM, Mahgoub HA, Ateya AI (2020). Ameliorative effect of curcumin against lead acetate–induced hemato-biochemical alterations, hepatotoxicity, and testicular oxidative damage in rats. Environ Sci Pollut Res, 27, 10950-10965.
  • Abdel-Daim MM, Alkahtani S, Almeer R, Albasher G (2020). 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, 27 (27), 33723-33731.
  • Abdel-Emam RA, Ali MF (2022). Effect of L-carnitine supplementation on lead acetate-induced liver cell apoptosis and inflammation: Role of caspase-3 and glycogen synthase kinase-3β enzymes. Life Sci, 291, 120277.
  • Aboutalebi S, Zare N, Sheikhzadeh P (2023). Physio-biochemical response of Borago officinalis L. roots to cadmium toxicity. Russ J Plant Physl, 70 (3), 37.
  • Afkhami-Ardakani M, Hassanzadeh S, Shahrooz R et al. (2017). Phytotherapy and phytopharmacology for reduction of cyclophosphamide-induced toxicity in the male urinary system. J Renal Inj Prev, 6 (3), 164-170.
  • Akhavan N, Parikh K, Salazar G, Arjmandi B (2020). The antioxidative effects of Borago officinalis in lipopolysaccharide and hydrogen peroxide-activated RAW 264.7 macrophages. Curr dev nutr, 4, 045-001.
  • Badary DM (2017). Folic acid protects against lead acetate-induced hepatotoxicity by decreasing NF-κB, IL-1β production and lipid peroxidation mediataed cell injury. Pathophysiology, 24 (1), 39-44.
  • Balakin AA, Minigalieva IA, Kuznetsov DA et al. (2024). Dose dependency of subchronic lead acetate exposure on biophysical characteristics of rats’ right atrium and ventricle. Eur Phys J Spec Top, 233 (23), 3507-3517.
  • Bolat İ, Bolat M, Kiliçlioğlu M et al. (2025a). Differential TLR2 and TLR4 mediated inflammatory and apoptotic responses in asymptomatic and symptomatic Leptospira interrogans infections in canine uterine tissue. Microb Pathog, 198, 107186.
  • Bolat M, Laçin B, Çelebi F (2024). Ratlarda Bisfenol-A’nın Neden Olduğu Nörotoksisite Üzerine Hesperidinin Etkilerinin Araştırılması. Vet sci and pract, 19 (1), 17-24.
  • Bolat M, Tekin S, Bolat İ et al. (2025b). Gallic acid’s protective mechanisms against acrylamide-induced pulmonary injury: in vivo and in silico insights into the Nrf-2/HO-1/NFκB pathway modulation. N-S Arch Pharmacol, 398, 11821–11837.
  • Chen C, Lin B, Qi S et al. (2019). Protective effects of salidroside on lead acetate-induced oxidative stress and hepatotoxicity in Sprague-Dawley rats. Biol Trace Elem Res, 191, 426-434.
  • Dogan T, Yıldırım BA, Kapakin KAT et al. (2025). Protective effects of crocin against gentamicin-induced damage in rat testicular tissue: modulating the levels of NF-κB/TLR-4 and Bax/Bcl-2/Caspase-3 signaling pathways. Food Chem Toxicol, 115407.
  • Din SR, Saeed, S, Khan SU et al. (2023). Bioactive compounds (BACs): A novel approach to treat and prevent cardiovascular diseases. Curr Probl Cardiol, 48 (7), 101664.
  • Feng L, Yang X, Shi Y et al. (2018): Co-exposure subacute toxicity of silica nanoparticles and lead acetate on cardiovascular system. Int J Nanomedicine, 7819-7834.
  • Gilani AH, Bashir S, Khan AU (2007). Pharmacological basis for the use of Borago officinalis in gastrointestinal, respiratory and cardiovascular disorders. J Ethnopharmacol, 114 (3), 393-399.
  • Harshitha P, Bose K, Dsouza HS (2024). Influence of lead-induced toxicity on the inflammatory cytokines. Toxicology, 503, 153771.
  • Ibrahim NM, Eweis EA, El-Beltagi HS, Abdel-Mobdy YE (2012). Effect of lead acetate toxicity on experimental male albino rat. Asian Pac J Trop Biomed, 2 (1), 41-46.
  • Ileriturk M, Benzer F, Aksu EH et al. (2021). Chrysin protects against testicular toxicity caused by lead acetate in rats with its antioxidant, anti‐inflammatory, and antiapoptotic properties. J Food Biochem, 45 (2), e13593.
  • Jasem SA, Abas AK (2022). Physiological Effect of Green Synthesized Silver Nanoparticles Agnps on Albino Rat Testis. Egypt J Hosp Med, 89 (2), 8076-8082.
  • Kmail A (2024) Mitigating digestive disorders: Action mechanisms of Mediterranean herbal active compounds. Open Life Sci,19 (1), 20220857.
  • Khattab HA, Abdallah IZ, Yousef FM, Huwait EA (2017). Efficiency of borage seeds oil against gamma irradiation-induced hepatotoxicity in male rats: possible antioxidant activity. Afr J Tradit Complement Altern Med, 14 (4), 169-179.
  • Li C, Shi L, Peng C et al. (2021). Lead-induced cardiomyocytes apoptosis by inhibiting gap junction intercellular communication via autophagy activation. Chem Biol Interact, 337, 109331.
  • Li Y, Cai W, Ai Z et al. (2023). Protective effects of sinomenine hydrochloride on lead-induced oxidative stress, inflammation, and apoptosis in mouse liver. Environ Sci Pollut Res Int, 30 (3), 7510-7521.
  • Mohammadi M, Rashidizad SA, Lashkari N et al. (2020). Supplement Therapy in Multiple Sclerosis: A Pharmacological View. Avicenna J Pharm Res, 1 (1), 37-45.
  • Oluranti OI, Adeyemo VA, Achile EO et al. (2022). Rutin improves cardiac and erythrocyte membrane–bound ATPase activities in male rats exposed to cadmium chloride and lead acetate. Biol Trace Elem Res, 1-9.
  • Ovie FO, Nwanama EK, Nwafor CC et al. (2023). Nephroprotective effects of Cajanus cajan on lead acetate-induced kidney damage of male Wistar rats. J. Clin. Exp. Med., 20 (2), 50-54.
  • Owumi SE, Otunla MT, Arunsi UO (2023). A biochemical and histology experimental approach to investigate the adverse effect of chronic lead acetate and dietary furan on rat lungs. Biometals, 36 (1), 201-216.
  • Oyem JC, Chris-Ozoko LE, Enaohwo MT et al. (2021). Antioxidative properties of Ocimum gratissimum alters Lead acetate induced oxidative damage in lymphoid tissues and hematological parameters of adult Wistar rats. Toxicol rep, 8, 215-222.
  • Rahman S, Sultana S (2006). Chemopreventive activity of glycyrrhizin on lead acetate mediated hepatic oxidative stress and its hyperproliferative activity in Wistar rats. Chem Biol Interact, 160 (1), 61-69.
  • Riaz T, Akram M, Laila U et al. (2023). Anti-inflammatory activity of medicinal plants and herbs: A review. IAIM 10 (12).
  • Samarghandian S, Borji A, Afshari R et al. (2013). The effect of lead acetate on oxidative stress and antioxidant status in rat bronchoalveolar lavage fluid and lung tissue. Toxicol Mech Methods, 23 (6), 432-436.
  • Şimşek H, Küçükler S, Gür C et al. (2023). Protective effects of sinapic acid against lead acetate-induced nephrotoxicity: a multi-biomarker approach. Environ Sci Pollut Res Int, 30 (45), 101208-101222.
  • Tanwar B, Goyal A, Kumar V et al. (2021). Borage (Borago officinalis) seed. OHFA, 351-371.
  • Torun H, Eroğlu E (2021). Antioxidant defense system in Borago officinalis L. under drought stress. TURKJANS, 8 (4), 1048-1055.
  • Tuncer SÇ, Akarsu SA, Küçükler S et al. (2023). Effects of sinapic acid on lead acetate‐induced oxidative stress, apoptosis and inflammation in testicular tissue. Environ toxicol, 38 (11), 2656-2667.
  • Zhou L, Wang S, Cao L et al. (2021). Lead acetate induces apoptosis in Leydig cells by activating PPARγ/caspase-3/PARP pathway. Int J Environ Health Res, 31 (1), 34-44.
There are 37 citations in total.

Details

Primary Language English
Subjects Veterinary Anatomy and Physiology, Veterinary Pathology
Journal Section Research Article
Authors

Merve Bolat 0000-0001-5836-5529

İsmail Bolat 0000-0003-1398-7046

Samet Tekin 0000-0003-4116-6720

Fikret Çelebi 0000-0002-6196-2196

Early Pub Date November 30, 2025
Publication Date November 30, 2025
Submission Date September 1, 2025
Acceptance Date October 21, 2025
Published in Issue Year 2025 Volume: 36 Issue: 3

Cite

APA Bolat, M., Bolat, İ., Tekin, S., Çelebi, F. (2025). The Effect of Borage Oil (Borago officinalis) on Lead Acetate-Induced Cardiotoxicity. Van Veterinary Journal, 36(3), 254-260. https://doi.org/10.36483/vanvetj.1774021
AMA Bolat M, Bolat İ, Tekin S, Çelebi F. The Effect of Borage Oil (Borago officinalis) on Lead Acetate-Induced Cardiotoxicity. Van Vet J. November 2025;36(3):254-260. doi:10.36483/vanvetj.1774021
Chicago Bolat, Merve, İsmail Bolat, Samet Tekin, and Fikret Çelebi. “The Effect of Borage Oil (Borago Officinalis) on Lead Acetate-Induced Cardiotoxicity”. Van Veterinary Journal 36, no. 3 (November 2025): 254-60. https://doi.org/10.36483/vanvetj.1774021.
EndNote Bolat M, Bolat İ, Tekin S, Çelebi F (November 1, 2025) The Effect of Borage Oil (Borago officinalis) on Lead Acetate-Induced Cardiotoxicity. Van Veterinary Journal 36 3 254–260.
IEEE M. Bolat, İ. Bolat, S. Tekin, and F. Çelebi, “The Effect of Borage Oil (Borago officinalis) on Lead Acetate-Induced Cardiotoxicity”, Van Vet J, vol. 36, no. 3, pp. 254–260, 2025, doi: 10.36483/vanvetj.1774021.
ISNAD Bolat, Merve et al. “The Effect of Borage Oil (Borago Officinalis) on Lead Acetate-Induced Cardiotoxicity”. Van Veterinary Journal 36/3 (November2025), 254-260. https://doi.org/10.36483/vanvetj.1774021.
JAMA Bolat M, Bolat İ, Tekin S, Çelebi F. The Effect of Borage Oil (Borago officinalis) on Lead Acetate-Induced Cardiotoxicity. Van Vet J. 2025;36:254–260.
MLA Bolat, Merve et al. “The Effect of Borage Oil (Borago Officinalis) on Lead Acetate-Induced Cardiotoxicity”. Van Veterinary Journal, vol. 36, no. 3, 2025, pp. 254-60, doi:10.36483/vanvetj.1774021.
Vancouver 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):254-60.

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