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Investigation of the Effect of Borago officinalis on Bax/Bcl-2/Caspase-3 Pathways Against Spleen Toxicity Induced by Lead Acetate in Rats

Yıl 2025, Cilt: 36 Sayı: 2, 132 - 138, 27.07.2025
https://doi.org/10.36483/vanvetj.1683003

Öz

Lead is a highly toxic heavy metal and an environmental pollutant. Lead exposure causes damage and dysfunctions in organs. In tissues exposed to lead, ROS increase, resulting in oxidative stress, inflammation and apoptosis. In this study, we aimed to investigate the protective effects of Borago officinalis (BO) against lead, whose toxic effects are well-established. In this study, 40 Sprague-Dawley rats were used. The rats were randomly divided into 5 groups. The groups were determined as control, BO100, Pb (20 mg/kg), Pb+BO50 and Pb+BO100. After the experimental procedures were completed, the tissues were transported in cold chain and stored in -80 deep freezer until the experiments were performed. Keap-1 level was determined in spleen tissue using Western blot method. At the same time, IL-1β, IL-10, NF-ĸB, Bax, Bcl-2, Caspase-3 levels were determined by RT-PCR method. BO administration stimulated Keap-1 level in relation to oxidative stress. While BO suppressed IL-1β and NF-ĸB levels, it stimulated IL-10 level, which are anti-inflammatory markers. BO also suppressed Bax and Kaspas-3 levels, while significantly stimulating Bcl-2 level. With these effects, it was observed that BO had anti-oxidant, anti-inflammatory, anti-apoptotic effects in the spleen tissue of rats treated with lead acetate.

Etik Beyan

This study was carried out with the permission of Atatürk University Animal Experiments Local Ethics Committee dated 10/03/2025 and numbered E-36643897-000-2500089778.

Kaynakça

  • Abbaszadeh S, Yadegari P, Imani A, Taghdir M (2021). Vitamin D3 protects against lead-induced testicular toxicity by modulating Nrf2 and NF-kappaB genes expression in rat. Reprod Toxicol, 103, 36-45.
  • 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 Int, 27, 10950-65.
  • Abubakar K, Muhammad Mailafiya M, Danmaigoro A et al. (2019). Curcumin Attenuates Lead-Induced Cerebellar Toxicity in Rats via Chelating Activity and Inhibition of Oxidative Stress. Biomolecules, 9.
  • Akaras N, Gur C, Kucukler S, Kandemir FM (2023). Zingerone reduces sodium arsenite-induced nephrotoxicity by regulating oxidative stress, inflammation, apoptosis and histopathological changes. Chem Biol Interact, 374, 110410.
  • Aksu EH, Kandemir FM, Kucukler S (2021). Ameliorative effect of hesperidin on streptozotocin-diabetes mellitus-induced testicular DNA damage and sperm quality degradation in Sprague-Dawley rats. J Food Biochem, 45, e13938.
  • Al-Megrin WA, Alkhuriji AF, Yousef AOS et al. (2019). Antagonistic Efficacy of Luteolin against Lead Acetate Exposure-Associated with Hepatotoxicity is Mediated via Antioxidant, Anti-Inflammatory, and Anti-Apoptotic Activities. Antioxidants (Basel), 9.
  • Alhusaini AM, Faddah LM, Hasan IH et al. (2019). Vitamin C and Turmeric Attenuate Bax and Bcl-2 Proteins' Expressions and DNA Damage in Lead Acetate-Induced Liver Injury. Dose Response, 17, 1559325819885782.
  • 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 (1), 22-28.
  • Bamboat ZM, Ocuin LM, Balachandran VP et al. (2010). Conventional DCs reduce liver ischemia/reperfusion injury in mice via IL-10 secretion. J Clin Invest, 120, 559-569.
  • Bidanchi RM, Lalrindika L, Khushboo M et al. (2022). Antioxidative, anti-inflammatory and anti-apoptotic action of ellagic acid against lead acetate induced testicular and hepato-renal oxidative damages and pathophysiological changes in male Long Evans rats. Environ Pollut, 302, 119048.
  • Cesta MF (2006). Normal structure, function, and histology of the spleen. Toxicol Pathol, 34, 455-465.
  • Cheng Q, Jiang S, Huang L et al. (2019). Zearalenone induced oxidative stress in the jejunum in postweaning gilts through modulation of the Keap1-Nrf2 signaling pathway and relevant genes1. J Anim Sci, 97, 1722-1733.
  • Dahran N, Alobaidy MA, Owaydhah WH et al. (2025). Polydatin Mitigates Lead-Induced Nephropathy by Modulating Oxidative Stress, Inflammation, and the AMPK/AKT/Nrf2 Pathway in Rats. Biol Trace Elem Res, DOI: 10.1007/s12011-025-04570-9.
  • Dkhil MA, Moneim AE, Al-Quraishy S (2016). Indigofera oblongifolia Ameliorates Lead Acetate-Induced Testicular Oxidative Damage and Apoptosis in a Rat Model. Biol Trace Elem Res, 173, 354-361.
  • Frank JJ, Poulakos AG, Tornero-Velez R, Xue J (2019). Systematic review and meta-analyses of lead (Pb) concentrations in environmental media (soil, dust, water, food, and air) reported in the United States from 1996 to 2016. Sci Total Environ, 694, 133489.
  • Friling RS, Bensimon A, Tichauer Y, Daniel V (1990). Xenobiotic-inducible expression of murine glutathione S-transferase Ya subunit gene is controlled by an electrophile-responsive element. Proc Natl Acad Sci U S A, 87, 6258-6262.
  • Ghahremanitamadon F, Shahidi S, Zargooshnia S et al. (2014). Protective effects of Borago officinalis extract on amyloid beta-peptide(25-35)-induced memory impairment in male rats: a behavioral study. Biomed Res Int, 2014, 798535.
  • Gupta RC (2018). Veterinary Toxicology Basic and Clinical Principles Third Edition Preface. Veterinary Toxicology: Basic and Clinical Principles, 3rd Edition, Xxxi-Xxxii.
  • Harshitha P, Bose K, Dsouza HS (2024). Influence of lead-induced toxicity on the inflammatory cytokines. Toxicology, 503, 153771.
  • He Y, Tan D, Mi Y, Zhou Q, Ji S (2017). Epigallocatechin-3-gallate attenuates cerebral cortex damage and promotes brain regeneration in acrylamide-treated rats. Food Funct, 8, 2275-2282.
  • Itoh K, Chiba T, Takahashi S et al. (1997). An Nrf2/small Maf heterodimer mediates the induction of phase II detoxifying enzyme genes through antioxidant response elements. Biochem Biophys Res Commun, 236, 313-322.
  • Jaramillo MC, Zhang DD (2013). The emerging role of the Nrf2-Keap1 signaling pathway in cancer. Genes Dev, 27, 2179-2191.
  • Jiang X, Xing X, Zhang Y et al. (2021). Lead exposure activates the Nrf2/Keap1 pathway, aggravates oxidative stress, and induces reproductive damage in female mice. Ecotoxicol Environ Saf, 207, 111231.
  • Kandemir FM, Yildirim S, Kucukler S et al. (2020). Protective effects of morin against acrylamide-induced hepatotoxicity and nephrotoxicity: A multi-biomarker approach. Food Chem Toxicol, 138, 111190.
  • Karimi E, Oskoueian E, Karimi A, Noura R, Ebrahimi M (2018). L. flower: a comprehensive study on bioactive compounds and its health-promoting properties. Journal of Food Measurement and Characterization, 12, 826-38.
  • Khattab HAH, Abdallah IZA, 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, 169-79.
  • Kucukler S, Benzer F, Yildirim S et al. (2021). Protective Effects of Chrysin Against Oxidative Stress and Inflammation Induced by Lead Acetate in Rat Kidneys: a Biochemical and Histopathological Approach. Biol Trace Elem Res, 199, 1501-14.
  • Kuzu M, Kandemir FM, Yildirim S et al. (2018). Morin attenuates doxorubicin-induced heart and brain damage by reducing oxidative stress, inflammation and apoptosis. Biomed Pharmacother, 106, 443-453.
  • Lewis SM, Williams A, Eisenbarth SC (2019). Structure and function of the immune system in the spleen. Sci Immunol, 4 (33), e:eaau6085.
  • Li L, Wang S, Zhou W (2022). Balance Cell Apoptosis and Pyroptosis of Caspase-3-Activating Chemotherapy for Better Antitumor Therapy. Cancers (Basel), 15 (1), 26.
  • Liu J, Li L, Wang Y, Yan C, Liu X (2013). Impact of low blood lead concentrations on IQ and school performance in Chinese children. PLoS One, 8, e65230.
  • Lukivskaya OY, Naruta E, Sadovnichy V, Kirko S, Buko VU (2012). Reversal of experimental ethanol-induced liver steatosis by borage oil. Phytother Res, 26, 1626-1631.
  • Monari S, Ferri M, Zappi A et al. (2025). Bioaccessibility and Biological Activities of Phytochemicals from Wild Plant Infusions and Decoctions Before and After Simulated In Vitro Digestion. Plant Foods Hum Nutr, 80, 81.
  • Munir N, Jahangeer M, Bouyahya A et al. (2022). Heavy Metal Contamination of Natural Foods Is a Serious Health Issue: A Review. Sustainability, 14.
  • Obeng-Gyasi E, Roostaei J, Gibson JM (2021). Lead Distribution in Urban Soil in a Medium-Sized City: Household-Scale Analysis. Environ Sci Technol, 55, 3696-3705.
  • Pieszak M, Mikolajczak PL, Manikowska K (2012). Borage (Borago officinalis L.)-a valuable medicinal plant used in herbal medicine. Herba Polonica, 58.
  • Ruff HA, Markowitz ME, Bijur PE, Rosen JF (1996). Relationships among blood lead levels, iron deficiency, and cognitive development in two-year-old children. Environ Health Perspect, 104, 180-185.
  • Shannon MW, Graef JW (1992). Lead intoxication in infancy. Pediatrics, 89, 87-90.
  • Simsek H, Demiryürek S, Demir T et al. (2016). Assessment of expressions of Bcl-XL, b-FGF, Bmp-2, Caspase-3, PDGFR-α, Smad1 and TGF-β1 genes in a rat model of lung ischemia/reperfusion. IJBMS, 19, 209-214.
  • Simsek H, Gur C, Kucukler S et al. (2024). Carvacrol Reduces Mercuric Chloride-Induced Testicular Toxicity by Regulating Oxidative Stress, Inflammation, Apoptosis, Autophagy, and Histopathological Changes. Biol Trace Elem Res, 202, 4605-4617.
  • Wang CL, Chuang HY, Ho CK et al. (2002). Relationship between blood lead concentrations and learning achievement among primary school children in Taiwan. Environ Res, 89, 12-18.
  • Ye F, Li X, Li L, Yuan J, Chen J (2016). t-BHQ Provides Protection against Lead Neurotoxicity via Nrf2/HO-1 Pathway. Oxid Med Cell Longev, 2016, 2075915.
  • Yu L, Li HX, Guo JY et al. (2019). Di (2-ethyl hexyl) phthalate (DEHP)-induced spleen toxicity in quail (Coturnix japonica) via disturbing Nrf2-mediated defense response. Environ Pollut, 251, 984-989.

Ratlarda Kurşun Asetat ile İndüklenen Dalak Toksisitesine Karşı Borago officinalis'in Bax/Bcl-2/Kaspaz-3 yolakları üzerine Etkisinin İncelenmesi

Yıl 2025, Cilt: 36 Sayı: 2, 132 - 138, 27.07.2025
https://doi.org/10.36483/vanvetj.1683003

Öz

Kurşun oldukça toksik bir ağır metal olup ve çevresel bir kirleticidir. Kurşun maruziyeti organlarda hasara ve fonksiyon bozukluklarına neden olmaktadır. Kurşuna maruz kalan dokularda ROS artışı buna bağlı, oksidatif stres, inflamasyon ve apoptosis şekillenmektedir. Biz bu çalışmada etkileri bilinen kurşuna karşı Borago officinalis (BO)’nun koruyucu etkilerini araştırmayı amaçladık. Bu çalışmada, 40 adet Sprague- Dawley cinsi ratlar kullanıldı. Ratlar rastgele 5 gruba ayrıldı. Gruplar kontrol, BO100, Pb (20 mg/kg), Pb+BO50 ve Pb+BO100 olarak belirlendi. Deney uygulamaları tamamlandıktan sonra, dokular soğuk zincirde taşınarak, deneylerin yapılıncaya kadar -80 derin dondurucuda saklandı. Dalak dokusunda Western Blot yöntemi kullanılarak Keap-1 düzeyi belirlendi. Aynı zamanda RT-PCR yöntemi kullanılarak IL-1β, IL-10, NF-ĸB, Bax, Bcl-2, Kaspaz-3 düzeyleri belirlendi. BO uygulaması oksidatif stresle ilgili olarak Keap-1 düzeyini uyardı. BO, IL-1β ve NF-ĸB düzeyini baskılarken, anti-inflamatuar markırlar olan IL-10 düzeyini uyardığı belirlendi. BO aynı zamanda Bax ve Kaspas-3 seviyesini baskılarken, Bcl-2 seviyesini önemli ölçüde uyarmaktadır. BO bu etkileriyle kurşun asetat uygulanan ratların dalak dokusunda anti-oksidan, anti-inflamatuar, anti-apoptotik etkilere sahip olduğu gözlendi.

Etik Beyan

Bu çalışma Atatürk Üniversitesi Hayvan Deneyleri Yerel Etik Kurulu'nun 10/03/2025 tarih ve E-36643897-000-2500089778 sayılı izni ile gerçekleştirilmiştir.

Kaynakça

  • Abbaszadeh S, Yadegari P, Imani A, Taghdir M (2021). Vitamin D3 protects against lead-induced testicular toxicity by modulating Nrf2 and NF-kappaB genes expression in rat. Reprod Toxicol, 103, 36-45.
  • 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 Int, 27, 10950-65.
  • Abubakar K, Muhammad Mailafiya M, Danmaigoro A et al. (2019). Curcumin Attenuates Lead-Induced Cerebellar Toxicity in Rats via Chelating Activity and Inhibition of Oxidative Stress. Biomolecules, 9.
  • Akaras N, Gur C, Kucukler S, Kandemir FM (2023). Zingerone reduces sodium arsenite-induced nephrotoxicity by regulating oxidative stress, inflammation, apoptosis and histopathological changes. Chem Biol Interact, 374, 110410.
  • Aksu EH, Kandemir FM, Kucukler S (2021). Ameliorative effect of hesperidin on streptozotocin-diabetes mellitus-induced testicular DNA damage and sperm quality degradation in Sprague-Dawley rats. J Food Biochem, 45, e13938.
  • Al-Megrin WA, Alkhuriji AF, Yousef AOS et al. (2019). Antagonistic Efficacy of Luteolin against Lead Acetate Exposure-Associated with Hepatotoxicity is Mediated via Antioxidant, Anti-Inflammatory, and Anti-Apoptotic Activities. Antioxidants (Basel), 9.
  • Alhusaini AM, Faddah LM, Hasan IH et al. (2019). Vitamin C and Turmeric Attenuate Bax and Bcl-2 Proteins' Expressions and DNA Damage in Lead Acetate-Induced Liver Injury. Dose Response, 17, 1559325819885782.
  • 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 (1), 22-28.
  • Bamboat ZM, Ocuin LM, Balachandran VP et al. (2010). Conventional DCs reduce liver ischemia/reperfusion injury in mice via IL-10 secretion. J Clin Invest, 120, 559-569.
  • Bidanchi RM, Lalrindika L, Khushboo M et al. (2022). Antioxidative, anti-inflammatory and anti-apoptotic action of ellagic acid against lead acetate induced testicular and hepato-renal oxidative damages and pathophysiological changes in male Long Evans rats. Environ Pollut, 302, 119048.
  • Cesta MF (2006). Normal structure, function, and histology of the spleen. Toxicol Pathol, 34, 455-465.
  • Cheng Q, Jiang S, Huang L et al. (2019). Zearalenone induced oxidative stress in the jejunum in postweaning gilts through modulation of the Keap1-Nrf2 signaling pathway and relevant genes1. J Anim Sci, 97, 1722-1733.
  • Dahran N, Alobaidy MA, Owaydhah WH et al. (2025). Polydatin Mitigates Lead-Induced Nephropathy by Modulating Oxidative Stress, Inflammation, and the AMPK/AKT/Nrf2 Pathway in Rats. Biol Trace Elem Res, DOI: 10.1007/s12011-025-04570-9.
  • Dkhil MA, Moneim AE, Al-Quraishy S (2016). Indigofera oblongifolia Ameliorates Lead Acetate-Induced Testicular Oxidative Damage and Apoptosis in a Rat Model. Biol Trace Elem Res, 173, 354-361.
  • Frank JJ, Poulakos AG, Tornero-Velez R, Xue J (2019). Systematic review and meta-analyses of lead (Pb) concentrations in environmental media (soil, dust, water, food, and air) reported in the United States from 1996 to 2016. Sci Total Environ, 694, 133489.
  • Friling RS, Bensimon A, Tichauer Y, Daniel V (1990). Xenobiotic-inducible expression of murine glutathione S-transferase Ya subunit gene is controlled by an electrophile-responsive element. Proc Natl Acad Sci U S A, 87, 6258-6262.
  • Ghahremanitamadon F, Shahidi S, Zargooshnia S et al. (2014). Protective effects of Borago officinalis extract on amyloid beta-peptide(25-35)-induced memory impairment in male rats: a behavioral study. Biomed Res Int, 2014, 798535.
  • Gupta RC (2018). Veterinary Toxicology Basic and Clinical Principles Third Edition Preface. Veterinary Toxicology: Basic and Clinical Principles, 3rd Edition, Xxxi-Xxxii.
  • Harshitha P, Bose K, Dsouza HS (2024). Influence of lead-induced toxicity on the inflammatory cytokines. Toxicology, 503, 153771.
  • He Y, Tan D, Mi Y, Zhou Q, Ji S (2017). Epigallocatechin-3-gallate attenuates cerebral cortex damage and promotes brain regeneration in acrylamide-treated rats. Food Funct, 8, 2275-2282.
  • Itoh K, Chiba T, Takahashi S et al. (1997). An Nrf2/small Maf heterodimer mediates the induction of phase II detoxifying enzyme genes through antioxidant response elements. Biochem Biophys Res Commun, 236, 313-322.
  • Jaramillo MC, Zhang DD (2013). The emerging role of the Nrf2-Keap1 signaling pathway in cancer. Genes Dev, 27, 2179-2191.
  • Jiang X, Xing X, Zhang Y et al. (2021). Lead exposure activates the Nrf2/Keap1 pathway, aggravates oxidative stress, and induces reproductive damage in female mice. Ecotoxicol Environ Saf, 207, 111231.
  • Kandemir FM, Yildirim S, Kucukler S et al. (2020). Protective effects of morin against acrylamide-induced hepatotoxicity and nephrotoxicity: A multi-biomarker approach. Food Chem Toxicol, 138, 111190.
  • Karimi E, Oskoueian E, Karimi A, Noura R, Ebrahimi M (2018). L. flower: a comprehensive study on bioactive compounds and its health-promoting properties. Journal of Food Measurement and Characterization, 12, 826-38.
  • Khattab HAH, Abdallah IZA, 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, 169-79.
  • Kucukler S, Benzer F, Yildirim S et al. (2021). Protective Effects of Chrysin Against Oxidative Stress and Inflammation Induced by Lead Acetate in Rat Kidneys: a Biochemical and Histopathological Approach. Biol Trace Elem Res, 199, 1501-14.
  • Kuzu M, Kandemir FM, Yildirim S et al. (2018). Morin attenuates doxorubicin-induced heart and brain damage by reducing oxidative stress, inflammation and apoptosis. Biomed Pharmacother, 106, 443-453.
  • Lewis SM, Williams A, Eisenbarth SC (2019). Structure and function of the immune system in the spleen. Sci Immunol, 4 (33), e:eaau6085.
  • Li L, Wang S, Zhou W (2022). Balance Cell Apoptosis and Pyroptosis of Caspase-3-Activating Chemotherapy for Better Antitumor Therapy. Cancers (Basel), 15 (1), 26.
  • Liu J, Li L, Wang Y, Yan C, Liu X (2013). Impact of low blood lead concentrations on IQ and school performance in Chinese children. PLoS One, 8, e65230.
  • Lukivskaya OY, Naruta E, Sadovnichy V, Kirko S, Buko VU (2012). Reversal of experimental ethanol-induced liver steatosis by borage oil. Phytother Res, 26, 1626-1631.
  • Monari S, Ferri M, Zappi A et al. (2025). Bioaccessibility and Biological Activities of Phytochemicals from Wild Plant Infusions and Decoctions Before and After Simulated In Vitro Digestion. Plant Foods Hum Nutr, 80, 81.
  • Munir N, Jahangeer M, Bouyahya A et al. (2022). Heavy Metal Contamination of Natural Foods Is a Serious Health Issue: A Review. Sustainability, 14.
  • Obeng-Gyasi E, Roostaei J, Gibson JM (2021). Lead Distribution in Urban Soil in a Medium-Sized City: Household-Scale Analysis. Environ Sci Technol, 55, 3696-3705.
  • Pieszak M, Mikolajczak PL, Manikowska K (2012). Borage (Borago officinalis L.)-a valuable medicinal plant used in herbal medicine. Herba Polonica, 58.
  • Ruff HA, Markowitz ME, Bijur PE, Rosen JF (1996). Relationships among blood lead levels, iron deficiency, and cognitive development in two-year-old children. Environ Health Perspect, 104, 180-185.
  • Shannon MW, Graef JW (1992). Lead intoxication in infancy. Pediatrics, 89, 87-90.
  • Simsek H, Demiryürek S, Demir T et al. (2016). Assessment of expressions of Bcl-XL, b-FGF, Bmp-2, Caspase-3, PDGFR-α, Smad1 and TGF-β1 genes in a rat model of lung ischemia/reperfusion. IJBMS, 19, 209-214.
  • Simsek H, Gur C, Kucukler S et al. (2024). Carvacrol Reduces Mercuric Chloride-Induced Testicular Toxicity by Regulating Oxidative Stress, Inflammation, Apoptosis, Autophagy, and Histopathological Changes. Biol Trace Elem Res, 202, 4605-4617.
  • Wang CL, Chuang HY, Ho CK et al. (2002). Relationship between blood lead concentrations and learning achievement among primary school children in Taiwan. Environ Res, 89, 12-18.
  • Ye F, Li X, Li L, Yuan J, Chen J (2016). t-BHQ Provides Protection against Lead Neurotoxicity via Nrf2/HO-1 Pathway. Oxid Med Cell Longev, 2016, 2075915.
  • Yu L, Li HX, Guo JY et al. (2019). Di (2-ethyl hexyl) phthalate (DEHP)-induced spleen toxicity in quail (Coturnix japonica) via disturbing Nrf2-mediated defense response. Environ Pollut, 251, 984-989.
Toplam 43 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Hayvan Sağlığı Ekonomisi ve İşletmeciliği
Bölüm Araştırma Makalesi
Yazarlar

Samet Tekin 0000-0003-4116-6720

Furkan Aykurt 0000-0003-3115-3969

Burak Çınar 0009-0005-5001-2776

Ömer Yardımcı 0009-0006-2348-4986

Burak Batuhan Laçin 0000-0002-5701-3684

Merve Bolat 0000-0001-5836-5529

İsmail Bolat 0000-0003-1398-7046

Ali Cınar 0000-0002-3928-320X

Gönderilme Tarihi 25 Nisan 2025
Kabul Tarihi 14 Temmuz 2025
Yayımlanma Tarihi 27 Temmuz 2025
Yayımlandığı Sayı Yıl 2025 Cilt: 36 Sayı: 2

Kaynak Göster

APA Tekin, S., Aykurt, F., Çınar, B., … Yardımcı, Ö. (2025). Investigation of the Effect of Borago officinalis on Bax/Bcl-2/Caspase-3 Pathways Against Spleen Toxicity Induced by Lead Acetate in Rats. Van Veterinary Journal, 36(2), 132-138. https://doi.org/10.36483/vanvetj.1683003
AMA Tekin S, Aykurt F, Çınar B, vd. 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. Temmuz 2025;36(2):132-138. doi:10.36483/vanvetj.1683003
Chicago Tekin, Samet, Furkan Aykurt, Burak Çınar, Ömer Yardımcı, Burak Batuhan Laçin, Merve Bolat, İsmail Bolat, ve Ali Cınar. “Investigation of the Effect of Borago officinalis on Bax/Bcl-2/Caspase-3 Pathways Against Spleen Toxicity Induced by Lead Acetate in Rats”. Van Veterinary Journal 36, sy. 2 (Temmuz 2025): 132-38. https://doi.org/10.36483/vanvetj.1683003.
EndNote Tekin S, Aykurt F, Çınar B, Yardımcı Ö, Laçin BB, Bolat M, Bolat İ, Cınar A (01 Temmuz 2025) Investigation of the Effect of Borago officinalis on Bax/Bcl-2/Caspase-3 Pathways Against Spleen Toxicity Induced by Lead Acetate in Rats. Van Veterinary Journal 36 2 132–138.
IEEE S. Tekin, F. Aykurt, B. Çınar, Ö. Yardımcı, B. B. Laçin, M. Bolat, İ. Bolat, ve A. Cınar, “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, c. 36, sy. 2, ss. 132–138, 2025, doi: 10.36483/vanvetj.1683003.
ISNAD Tekin, Samet vd. “Investigation of the Effect of Borago officinalis on Bax/Bcl-2/Caspase-3 Pathways Against Spleen Toxicity Induced by Lead Acetate in Rats”. Van Veterinary Journal 36/2 (Temmuz2025), 132-138. https://doi.org/10.36483/vanvetj.1683003.
JAMA Tekin S, Aykurt F, Çınar B, Yardımcı Ö, Laçin BB, Bolat M, Bolat İ, Cınar A. 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;36:132–138.
MLA Tekin, Samet vd. “Investigation of the Effect of Borago officinalis on Bax/Bcl-2/Caspase-3 Pathways Against Spleen Toxicity Induced by Lead Acetate in Rats”. Van Veterinary Journal, c. 36, sy. 2, 2025, ss. 132-8, doi:10.36483/vanvetj.1683003.
Vancouver Tekin S, Aykurt F, Çınar B, Yardımcı Ö, Laçin BB, Bolat M, vd. 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):132-8.

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