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Effect of Borage Seed Oil Against Lead Acetate Neurotoxicity in Rats

Yıl 2026, Cilt: 37 Sayı: 1, 22 - 27, 29.03.2026
https://doi.org/10.36483/vanvetj.1789129
https://izlik.org/JA82MX92CY

Öz

Lead (Pb) is a highly toxic heavy metal that has long been widely used in industry, agriculture, and the cosmetics sector. It also poses serious public health risks due to its tendency to accumulate in the body and to induce pronounced neurotoxicity, particularly by damaging the central nervous system via oxidative stress–mediated mechanisms. In the present study, the biochemical effects of lead acetate-induced neurotoxicity and the potential protective role of borage seed oil (Borago oil, BSO), known for its high medicinal and nutritional value, were evaluated in the brain tissue of rats by assessing oxidative stress parameters. A total of 30 Sprague Dawley rats were randomly divided into five groups. Neurotoxicity was induced by intraperitoneal administration of lead acetate at a dose of 20 mg/kg for 7 consecutive days. Borage oil was administered orally at doses of 50 and 100 mg/kg for 14 days. Malondialdehyde (MDA) levels in the rat brain tissue were measured using manual biochemical method, while the expression levels of superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx) were determined by RT-PCR. Collectively, these findings indicate that borage seed oil partially alleviated Pb- associated oxidative stress alterationsin brain tissue, as evidenced by reduced lipid peroxidation (decreased MDA; p<0.001) and upregulated mRNA expression of antioxidant enzymes (SOD, CAT, and GPx) compared with the Pb group (overall ANOVA p<0.001; Tukey’s post hoc test). Moreover, the 100 mg/kg dose tended to produce greater improvements in oxidative stress–related parameters than the 50 mg/kg dose.

Kaynakça

  • Abdel Moneim AE, Dkhil MA, Al-Quraishy S (2011). Effects of flaxseed oil on lead acetate-induced neurotoxicity in rats. Biol Trace Elem Res, 144(1), 904–913.
  • Ali S, Naseer S, Rehman M, Wei Z (2024). Recent trends and sources of lead toxicity: A review of state-of-the-art nano-remediation strategies. J Nanopart Res, 26(7), 168.
  • Alqahtani WS, Albasher G (2021). Moringa oleifera Lam. extract rescues lead-induced oxidative stress, inflammation, and apoptosis in the rat cerebral cortex. J Food Biochem, 45(1), e13579.
  • Asadi-Samani M, Bahmani M, Rafieian-Kopaei M (2014). The chemical composition, botanical characteristic and biological activities of Borago officinalis: a review. Asian Pac J Trop Med, 7, 22–28.
  • Bandonien D, Murkovic M (2002). The detection of radical scavenging compounds in crude extract of borage (Borago officinalis L.) by using an on-line HPLC-DPPH method. J Biochem Biophys Methods, 53, 45–49.
  • Barati E, Asl SS, Pourbakhsh SA, Jamshidian M, Shahidi S (2016). Effect of borage on hippocampal TNF-α protein and gene in the amyloid β-peptide (25–35)-induced Alzheimer model in rat. Biosci Biotechnol Res Asia, 13(1), 37–42.
  • Ben-Azu B, Adebayo OG, Wopara I et al. (2022). Lead acetate induces hippocampal pyramidal neuron degeneration in mice via up-regulation of executioner caspase-3, oxido-inflammatory stress expression and decreased BDNF and cholinergic activity: Reversal effects of Gingko biloba supplement. J Trace Elem Med Biol, 71, 126919.
  • Conforti F, Sosa S, Marrelli M et al. (2008). In vivo anti-inflammatory and in vitro antioxidant activities of Mediterranean dietary plants. J Ethnopharmacol, 116, 144–151.
  • Das UN (2006). Essential fatty acids: Biochemistry, physiology and pathology. Biotechnol J, 1, 420–439.
  • Famurewa AC, Renu K, Eladl MA et al. (2022). Hesperidin and hesperetin against heavy metal toxicity: Insight on the molecular mechanism of mitigation. Biomed Pharmacother, 149, 112914.
  • Farhadi R, Balashahri M, Tilebeni H, Sadeghi M (2012). Pharmacology of borage (Borago officinalis L.) medicinal plant. Int J Agron Plant Prod, 3(2), 73–77.
  • Ghahremanitamadon F, Shahidi S, Zargooshnia S et al. (2014). Protective effects of Borago officinalis extract on amyloid β-peptide (25–35)-induced memory impairment in male rats: A behavioral study. Biomed Res Int, 798535.
  • 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.
  • Kast RE (2001). Borage oil reduction of rheumatoid arthritis activity may be mediated by increased cAMP that suppresses tumor necrosis factor-alpha. Int Immunopharmacol, 1, 2197–2199.
  • Komaki A, Rasouli B, Shahidi S (2015). Anxiolytic effect of Borago officinalis (Boraginaceae) extract in male rats. Avicenna J Neuro Psycho, 2, 34–38.
  • Livak KJ, Schmittgen TD (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods, 25, 402–408.
  • Mhamdi B, Wannes WA, Bourgou S, Marzouk B (2009). Biochemical characterization of borage (Borago officinalis L.) seeds. J Food Biochem, 33, 331–341.
  • Michalak M, Zagórska-Dziok M, Klimek-Szczykutowicz M, Szopa A (2023). Phenolic profile and comparison of the antioxidant, anti-ageing, anti-inflammatory, and protective activities of Borago officinalis extracts on skin cells. Molecules, 28(2), 868.
  • Moliner C, Cásedas G, Barros L et al. (2022). Neuroprotective profile of edible flowers of borage (Borago officinalis L.) in two different models: Caenorhabditis elegans and Neuro-2a cells. Antioxidants, 11(7), 1244.
  • Neal AP, Guilarte TR (2010). Molecular neurobiology of lead (Pb2+): Effects on synaptic function. Mol Neurobiol, 42(3), 151–160.
  • Niu C, Dong M, Niu Y (2023). Lead toxicity and potential therapeutic effect of plant-derived polyphenols. Phytomedicine, 114, 154789.
  • Paduraru E, Flocea EI, Lazado CC et al. (2021). Vitamin C mitigates oxidative stress and behavioral impairments induced by deltamethrin and lead toxicity in zebrafish. Int J Mol Sci, 22, 12714.
  • Placer ZA, Cushman LL, Johnson BC (1966). Estimation of product of lipid peroxidation (malonyl dialdehyde) in biochemical systems. Anal Biochem, 16, 359–364.
  • Rahimi K, Nourishirazi A, Delaviz H, Ghotbeddin Z (2024). Antinociceptive effects of gamma-linolenic acid in the formalin test in the rats. Ann Med Surg, 86, 2677–2683.
  • Ramírez Ortega D, González Esquivel DF, Blanco Ayala T et al. (2021). Cognitive impairment induced by lead exposure during lifespan: Mechanisms of lead neurotoxicity. Toxics, 9, 23.
  • Saber TM, Abo-Elmaaty AMA, Said EN et al. (2022). Alhagi maurorum ethanolic extract rescues hepato-neurotoxicity and neurobehavioral alterations induced by lead in rats via abrogating oxidative stress and the caspase-3-dependent apoptotic pathway. Antioxidants, 11, 1992.
  • Seo SA, Park B, Hwang E, Park SY, Yi TH (2018). Borago officinalis L. attenuates UVB-induced skin photodamage via regulation of AP-1 and Nrf2/ARE pathway in normal human dermal fibroblasts and promotion of collagen synthesis in hairless mice. Exp Gerontol, 107, 178–186.
  • Singh PK, Nath R, Ahmad MK et al. (2016). Attenuation of lead neurotoxicity by supplementation of polyunsaturated fatty acid in Wistar rats. Nutr Neurosci, 19, 396–405.
  • Song XB, Liu G, Liu F et al. (2017). Autophagy blockade and lysosomal membrane permeabilization contribute to lead-induced nephrotoxicity in primary rat proximal tubular cells. Cell Death Dis, 8(6), 2863.
  • Tanwar B, Goyal A, Kumar V, Rasane P, Sihag MK (2021). Borage (Borago officinalis) seed. In: Oilseeds: Health Attributes and Food Applications, 351–371.
  • Velaga MK, Basuri CK, Robinson Taylor KS et al. (2014). Ameliorative effects of Bacopa monniera on lead-induced oxidative stress in different regions of rat brain. Drug Chem Toxicol, 37, 357–364.
  • Wainwright PE, Huang YS, DeMichele SJ et al. (2003). Effects of high-γ-linolenic acid canola oil compared with borage oil on reproduction, growth, and brain and behavioral development in mice. Lipids, 38, 171–178.
  • Yallapragada PR, Velaga MK (2015). Effect of Ginkgo biloba extract on lead-induced oxidative stress in different regions of rat brain. J Environ Pathol Toxicol Oncol, 34, 161–173.
  • Yao J, Qiao H, Jin Z et al. (2020). Ginkgo biloba and its constituent 6-hydroxykynurenic acid as well as its proanthocyanidins exert neurorestorative effects against cerebral ischemia. Planta Med, 86, 696–707.
  • Yipel M, Tekeli İO (2022). Essential and non-essential metal concentrations in shrimps from Iskenderun Bay, Türkiye. Harran Univ Vet Fak Derg, 11, 257–262.
  • Yousef AOS, Fahad AA, Moneim AEA et al. (2019). 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, 16, 2895.

Sıçanlarda Kurşun Asetat Nörotoksisitesine Karşı Hodan Tohum Yağının Etkisi

Yıl 2026, Cilt: 37 Sayı: 1, 22 - 27, 29.03.2026
https://doi.org/10.36483/vanvetj.1789129
https://izlik.org/JA82MX92CY

Öz

Kurşun (Pb), uzun süredir endüstri, tarım ve kozmetik sektörlerinde yaygın olarak kullanılan oldukça toksik bir ağır metaldir. Ayrıca vücutta birikme ve özellikle oksidatif stres aracılığıyla merkezi sinir sistemine zarar vererek belirgin nörotoksisiteye yol açma eğilimiyle ciddi halk sağlığı riskleri oluşturmaktadır. Bu çalışmada, yüksek tıbbi ve besinsel değeri ile bilinen hodan tohum yağının (Hodan yağı, BSO) potansiyel koruyucu rolü ve kurşun asetat kaynaklı nörotoksisitenin biyokimyasal etkileri, sıçanların beyin dokusunda oksidatif stres parametrelerinin değerlendirilmesi yoluyla araştırılmıştır. Toplam 30 Sprague Dawley sıçanı rastgele beş gruba ayrılmıştır. Nörotoksisite, 7 gün boyunca 20 mg/kg dozunda intraperitoneal kurşun asetat uygulamasıyla oluşturulmuştur. Hodan yağı 14 gün boyunca 50 ve 100 mg/kg dozlarında oral yoldan uygulanmıştır. Sıçan beyin dokusunda malondialdehit (MDA) düzeyleri manuel biyokimyasal metod kullanılarak ölçülürken, süperoksit dismutaz (SOD), katalaz (CAT) ve glutatyon peroksidaz (GPx) ekspresyon düzeyleri RT-PCR ile belirlenmiştir. Toplu olarak, bu bulgular, hodan tohumu yağının, kurşunla ilişkili oksidatif stres değişikliklerini beyin dokusunda kısmen hafiflettiğini göstermektedir; bu durum, kurşun grubuna kıyasla lipid peroksidasyonunda azalma (MDA'da azalma; p<0.001) ve antioksidan enzimlerin (SOD, CAT ve GPx) mRNA ekspresyonunda artış (genel ANOVA p<0.001; Tukey'in post hoc testi) ile kanıtlanmıştır. Dahası, 100 mg/kg dozu, 50 mg/kg dozuna kıyasla oksidatif stresle ilgili parametrelerde daha büyük iyileşmeler sağlama eğilimindeydi.

Kaynakça

  • Abdel Moneim AE, Dkhil MA, Al-Quraishy S (2011). Effects of flaxseed oil on lead acetate-induced neurotoxicity in rats. Biol Trace Elem Res, 144(1), 904–913.
  • Ali S, Naseer S, Rehman M, Wei Z (2024). Recent trends and sources of lead toxicity: A review of state-of-the-art nano-remediation strategies. J Nanopart Res, 26(7), 168.
  • Alqahtani WS, Albasher G (2021). Moringa oleifera Lam. extract rescues lead-induced oxidative stress, inflammation, and apoptosis in the rat cerebral cortex. J Food Biochem, 45(1), e13579.
  • Asadi-Samani M, Bahmani M, Rafieian-Kopaei M (2014). The chemical composition, botanical characteristic and biological activities of Borago officinalis: a review. Asian Pac J Trop Med, 7, 22–28.
  • Bandonien D, Murkovic M (2002). The detection of radical scavenging compounds in crude extract of borage (Borago officinalis L.) by using an on-line HPLC-DPPH method. J Biochem Biophys Methods, 53, 45–49.
  • Barati E, Asl SS, Pourbakhsh SA, Jamshidian M, Shahidi S (2016). Effect of borage on hippocampal TNF-α protein and gene in the amyloid β-peptide (25–35)-induced Alzheimer model in rat. Biosci Biotechnol Res Asia, 13(1), 37–42.
  • Ben-Azu B, Adebayo OG, Wopara I et al. (2022). Lead acetate induces hippocampal pyramidal neuron degeneration in mice via up-regulation of executioner caspase-3, oxido-inflammatory stress expression and decreased BDNF and cholinergic activity: Reversal effects of Gingko biloba supplement. J Trace Elem Med Biol, 71, 126919.
  • Conforti F, Sosa S, Marrelli M et al. (2008). In vivo anti-inflammatory and in vitro antioxidant activities of Mediterranean dietary plants. J Ethnopharmacol, 116, 144–151.
  • Das UN (2006). Essential fatty acids: Biochemistry, physiology and pathology. Biotechnol J, 1, 420–439.
  • Famurewa AC, Renu K, Eladl MA et al. (2022). Hesperidin and hesperetin against heavy metal toxicity: Insight on the molecular mechanism of mitigation. Biomed Pharmacother, 149, 112914.
  • Farhadi R, Balashahri M, Tilebeni H, Sadeghi M (2012). Pharmacology of borage (Borago officinalis L.) medicinal plant. Int J Agron Plant Prod, 3(2), 73–77.
  • Ghahremanitamadon F, Shahidi S, Zargooshnia S et al. (2014). Protective effects of Borago officinalis extract on amyloid β-peptide (25–35)-induced memory impairment in male rats: A behavioral study. Biomed Res Int, 798535.
  • 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.
  • Kast RE (2001). Borage oil reduction of rheumatoid arthritis activity may be mediated by increased cAMP that suppresses tumor necrosis factor-alpha. Int Immunopharmacol, 1, 2197–2199.
  • Komaki A, Rasouli B, Shahidi S (2015). Anxiolytic effect of Borago officinalis (Boraginaceae) extract in male rats. Avicenna J Neuro Psycho, 2, 34–38.
  • Livak KJ, Schmittgen TD (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods, 25, 402–408.
  • Mhamdi B, Wannes WA, Bourgou S, Marzouk B (2009). Biochemical characterization of borage (Borago officinalis L.) seeds. J Food Biochem, 33, 331–341.
  • Michalak M, Zagórska-Dziok M, Klimek-Szczykutowicz M, Szopa A (2023). Phenolic profile and comparison of the antioxidant, anti-ageing, anti-inflammatory, and protective activities of Borago officinalis extracts on skin cells. Molecules, 28(2), 868.
  • Moliner C, Cásedas G, Barros L et al. (2022). Neuroprotective profile of edible flowers of borage (Borago officinalis L.) in two different models: Caenorhabditis elegans and Neuro-2a cells. Antioxidants, 11(7), 1244.
  • Neal AP, Guilarte TR (2010). Molecular neurobiology of lead (Pb2+): Effects on synaptic function. Mol Neurobiol, 42(3), 151–160.
  • Niu C, Dong M, Niu Y (2023). Lead toxicity and potential therapeutic effect of plant-derived polyphenols. Phytomedicine, 114, 154789.
  • Paduraru E, Flocea EI, Lazado CC et al. (2021). Vitamin C mitigates oxidative stress and behavioral impairments induced by deltamethrin and lead toxicity in zebrafish. Int J Mol Sci, 22, 12714.
  • Placer ZA, Cushman LL, Johnson BC (1966). Estimation of product of lipid peroxidation (malonyl dialdehyde) in biochemical systems. Anal Biochem, 16, 359–364.
  • Rahimi K, Nourishirazi A, Delaviz H, Ghotbeddin Z (2024). Antinociceptive effects of gamma-linolenic acid in the formalin test in the rats. Ann Med Surg, 86, 2677–2683.
  • Ramírez Ortega D, González Esquivel DF, Blanco Ayala T et al. (2021). Cognitive impairment induced by lead exposure during lifespan: Mechanisms of lead neurotoxicity. Toxics, 9, 23.
  • Saber TM, Abo-Elmaaty AMA, Said EN et al. (2022). Alhagi maurorum ethanolic extract rescues hepato-neurotoxicity and neurobehavioral alterations induced by lead in rats via abrogating oxidative stress and the caspase-3-dependent apoptotic pathway. Antioxidants, 11, 1992.
  • Seo SA, Park B, Hwang E, Park SY, Yi TH (2018). Borago officinalis L. attenuates UVB-induced skin photodamage via regulation of AP-1 and Nrf2/ARE pathway in normal human dermal fibroblasts and promotion of collagen synthesis in hairless mice. Exp Gerontol, 107, 178–186.
  • Singh PK, Nath R, Ahmad MK et al. (2016). Attenuation of lead neurotoxicity by supplementation of polyunsaturated fatty acid in Wistar rats. Nutr Neurosci, 19, 396–405.
  • Song XB, Liu G, Liu F et al. (2017). Autophagy blockade and lysosomal membrane permeabilization contribute to lead-induced nephrotoxicity in primary rat proximal tubular cells. Cell Death Dis, 8(6), 2863.
  • Tanwar B, Goyal A, Kumar V, Rasane P, Sihag MK (2021). Borage (Borago officinalis) seed. In: Oilseeds: Health Attributes and Food Applications, 351–371.
  • Velaga MK, Basuri CK, Robinson Taylor KS et al. (2014). Ameliorative effects of Bacopa monniera on lead-induced oxidative stress in different regions of rat brain. Drug Chem Toxicol, 37, 357–364.
  • Wainwright PE, Huang YS, DeMichele SJ et al. (2003). Effects of high-γ-linolenic acid canola oil compared with borage oil on reproduction, growth, and brain and behavioral development in mice. Lipids, 38, 171–178.
  • Yallapragada PR, Velaga MK (2015). Effect of Ginkgo biloba extract on lead-induced oxidative stress in different regions of rat brain. J Environ Pathol Toxicol Oncol, 34, 161–173.
  • Yao J, Qiao H, Jin Z et al. (2020). Ginkgo biloba and its constituent 6-hydroxykynurenic acid as well as its proanthocyanidins exert neurorestorative effects against cerebral ischemia. Planta Med, 86, 696–707.
  • Yipel M, Tekeli İO (2022). Essential and non-essential metal concentrations in shrimps from Iskenderun Bay, Türkiye. Harran Univ Vet Fak Derg, 11, 257–262.
  • Yousef AOS, Fahad AA, Moneim AEA et al. (2019). 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, 16, 2895.
Toplam 36 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Veteriner Biyokimya
Bölüm Araştırma Makalesi
Yazarlar

Esra Aktas Senocak 0000-0003-1685-0803

Mustafa İleritürk 0000-0002-4581-4492

Gönderilme Tarihi 22 Eylül 2025
Kabul Tarihi 4 Şubat 2026
Yayımlanma Tarihi 29 Mart 2026
DOI https://doi.org/10.36483/vanvetj.1789129
IZ https://izlik.org/JA82MX92CY
Yayımlandığı Sayı Yıl 2026 Cilt: 37 Sayı: 1

Kaynak Göster

APA Aktas Senocak, E., & İleritürk, M. (2026). Effect of Borage Seed Oil Against Lead Acetate Neurotoxicity in Rats. Van Veterinary Journal, 37(1), 22-27. https://doi.org/10.36483/vanvetj.1789129
AMA 1.Aktas Senocak E, İleritürk M. Effect of Borage Seed Oil Against Lead Acetate Neurotoxicity in Rats. Van Vet J. 2026;37(1):22-27. doi:10.36483/vanvetj.1789129
Chicago Aktas Senocak, Esra, ve Mustafa İleritürk. 2026. “Effect of Borage Seed Oil Against Lead Acetate Neurotoxicity in Rats”. Van Veterinary Journal 37 (1): 22-27. https://doi.org/10.36483/vanvetj.1789129.
EndNote Aktas Senocak E, İleritürk M (01 Mart 2026) Effect of Borage Seed Oil Against Lead Acetate Neurotoxicity in Rats. Van Veterinary Journal 37 1 22–27.
IEEE [1]E. Aktas Senocak ve M. İleritürk, “Effect of Borage Seed Oil Against Lead Acetate Neurotoxicity in Rats”, Van Vet J, c. 37, sy 1, ss. 22–27, Mar. 2026, doi: 10.36483/vanvetj.1789129.
ISNAD Aktas Senocak, Esra - İleritürk, Mustafa. “Effect of Borage Seed Oil Against Lead Acetate Neurotoxicity in Rats”. Van Veterinary Journal 37/1 (01 Mart 2026): 22-27. https://doi.org/10.36483/vanvetj.1789129.
JAMA 1.Aktas Senocak E, İleritürk M. Effect of Borage Seed Oil Against Lead Acetate Neurotoxicity in Rats. Van Vet J. 2026;37:22–27.
MLA Aktas Senocak, Esra, ve Mustafa İleritürk. “Effect of Borage Seed Oil Against Lead Acetate Neurotoxicity in Rats”. Van Veterinary Journal, c. 37, sy 1, Mart 2026, ss. 22-27, doi:10.36483/vanvetj.1789129.
Vancouver 1.Esra Aktas Senocak, Mustafa İleritürk. Effect of Borage Seed Oil Against Lead Acetate Neurotoxicity in Rats. Van Vet J. 01 Mart 2026;37(1):22-7. doi:10.36483/vanvetj.1789129

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