Dergiler / Turkish Journal of Medical Sciences / 2019 / Cilt: 49 - Sayı: 5

Mid-dose losartan mitigates diabetes-induced hepatic damage by regulating iNOS, eNOS, VEGF, and NF-κB expressions

Sayfa
1582–1589
Yayın Tarihi
2022-11-05
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

In addition to immunohistochemical analysis, analyses of SOD and MDA, whichare oxidative stress markers, were also performed and the results were evaluated together.Results: When biochemical and immunohistochemical findings were evaluated together, it was found that the results obtained from themid-dose losartan group were closer to those of the control than the other groups.Conclusion: This study indicated that mid-dose losartan administration may have a therapeutic effect by inhibiting apoptosis andregulating iNOS, eNOS, VEGF, and NF-κB protein expressions in DM-induced hepatic damage.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Background/aim: Losartan, an antihypertensive drug, is highly preferred in patients with diabetes mellitus (DM) and hypertensionbecause of its retarding effect on diabetic nephropathy.
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Temel Bulgular & Veri:In this study, we investigated the potential therapeutic effect of different doses oflosartan on hepatic damage in a streptozotocin (STZ, 50 mg/kg)-induced DM model in rats.Materials and methods: In this study, five different groups were formed: control, DM, low-dose losartan (5 mg/kg), mid-dose losartan(20 mg/kg), and high-dose losartan (80 mg/kg).
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Sonuç & Katkı:In addition to immunohistochemical analysis, analyses of SOD and MDA, whichare oxidative stress markers, were also performed and the results were evaluated together.Results: When biochemical and immunohistochemical findings were evaluated together, it was found that the results obtained from themid-dose losartan group were closer to those of the control than the other groups.Conclusion: This study indicated that mid-dose losartan administration may have a therapeutic effect by inhibiting apoptosis andregulating iNOS, eNOS, VEGF, and NF-κB protein expressions in DM-induced hepatic damage.
🔬Tür:Modelleme & Sayısal Simülasyon
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Background/aim: Losartan, an antihypertensive drug, is highly preferred in patients with diabetes mellitus (DM) and hypertensionbecause of its retarding effect on diabetic nephropathy. In this study, we investigated the potential therapeutic effect of different doses oflosartan on hepatic damage in a streptozotocin (STZ, 50 mg/kg)-induced DM model in rats.Materials and methods: In this study, five different groups were formed: control, DM, low-dose losartan (5 mg/kg), mid-dose losartan(20 mg/kg), and high-dose losartan (80 mg/kg). Liver tissues of experimental groups were evaluated immunohistochemically forTUNEL, iNOS, eNOS, VEGF, and NF-κB pathways. In addition to immunohistochemical analysis, analyses of SOD and MDA, whichare oxidative stress markers, were also performed and the results were evaluated together.Results: When biochemical and immunohistochemical findings were evaluated together, it was found that the results obtained from themid-dose losartan group were closer to those of the control than the other groups.Conclusion: This study indicated that mid-dose losartan administration may have a therapeutic effect by inhibiting apoptosis andregulating iNOS, eNOS, VEGF, and NF-κB protein expressions in DM-induced hepatic damage.

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Bu Makaleye Atıf Yap

KÖSE, T., YAVAŞOĞLU, N. Ü. K., YAVAŞOĞLU, A., BUHUR, A., OLTULU, F., DAĞDEVİREN, M., KUŞÇU, G. C., GÜREL, Ç. (2022). Mid-dose losartan mitigates diabetes-induced hepatic damage by regulating iNOS, eNOS, VEGF, and NF-κB expressions. Turkish Journal of Medical Sciences, Cilt: 49 - Sayı: 5, 1582–1589. https://ajindex.com/articles/610202

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Kaynakça (12)

  1. Shi GJ, Li ZM, Zheng J, Chen J, Han XX et al. Diabetes associated with male reproductive system damages: onset of presentation, pathophysiological mechanisms and drug intervention. Biomedicine & Pharmacotherapy 2017
  2. doi: 10.1016/j.biopha.2017.03.074 2. Papadakis MA, McPhee SJ, Rabow MW. Current Medical Diagnosis & Treatment. 56th ed. San Francisco, CA, USA: McGraw-Hill Education
  3. American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care 2010
  4. 33 (1): 62-69. doi: 10.2337/dc10-S062 4. Ziamajidi N, Khaghani S, Hassanzadeh G, Vardasbi S, Ahmadian S et al. Amelioration by chicory seed extract of diabetes- and oleic acid-induced non-alcoholic fatty liver disease (NAFLD)/ non-alcoholic steatohepatitis (NASH) via modulation of PPARα and SREBP-1. Food and Chemical Toxicology 2013
  5. doi: 10.1016/j.fct.2013.04.018 5. Mukherjee P, Cinelli MA, Kang S, Silverman RB. Development of nitric oxide synthase inhibitors for neurodegeneration and neuropathic pain. Chemical Society Reviews 2014
  6. doi: 10.1039/c3cs60467e 6. Iwakiri Y, Kim MY. Nitric oxide in liver diseases. Trends in Pharmacological Sciences 2015
  7. 36 (8): 524-536. doi: 10.1016/j. tips.2015.05.001 7. Knowles RG, Moncada S. Nitric oxide synthases in mammals. Biochemical Journal 1994
  8. 298 (2): 249-258. doi: 10.1042/ bj2980249 8. Abu-Amara M, Yang SY, Seifalian A, Davidson B, Fuller B. The nitric oxide pathway - evidence and mechanisms for protection against liver ischaemia reperfusion injury. Liver International 2012
  9. 32 (4): 531-543. doi: 10.1111/j.1478-3231.2012.02755.x 9. Abdelmegeed MA, Song BJ. Functional roles of protein nitration in acute and chronic liver diseases. Oxidative Medicine and Cellular Longevity 2014
  10. 149627. doi: 10.1155/2014/149627 10. Madar Z, Kalet-Litman S, Stark AH. Inducible nitric oxide synthase activity and expression in liver and hepatocytes of diabetic rats. Pharmacology 2005
  11. 73 (2): 106-112. doi: 10.1159/000081952 11. Marazita MC, Dugour A, Marquioni-Ramella MD, Figueroa JM, Suburo AM. Oxidative stress-induced premature senescence dysregulates VEGF and CFH expression in retinal pigment epithelial cells: implications for age-related macular degeneration. Redox Biology 2016
  12. doi: 10.1016/j. redox.2015.11.011 12. Kroll J, Waltenberger J. VEGF-A induces expression of eNOS and iNOS in endothelial cells via VEGF receptor-2 (KDR). Biochemical and Biophysical Research Communications 199