Journals / Journal of Clinical and Analytical Medicine / 2014 / Cilt: 5 - Sayı: 6

Üzüm Çekirdeği Proanthocyanidin Özü (ÜÇPÖ) nün İdrar Sodyum Atılımı Üzerine Etkisi

The Effect of Grape Seed Proanthocyanidin Extract (GSPE) on Urinary Sodium Excretion

Pages
469–471
Publication Date
2022-10-18
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Na excretion waspositively correlated with solid food intake (p=0.029, r=0.583) and urine vol- ume (p

📌 3 Key Takeaways

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Objective & Hypothesis:Aim: While various hormones and mediators reduce the urinary excretion ofNa, other mediators such as nitric oxide (NO) increase Na excretion.
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Key Findings & Data:The control group was given 1 cm3milk by gavage for one week, while the GSPE group was given 100 mg/kgGSPE.
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Conclusion & Impact:Na excretion waspositively correlated with solid food intake (p=0.029, r=0.583) and urine vol- ume (p
🔬Design:Lab & Field Experiment
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Aim: While various hormones and mediators reduce the urinary excretion ofNa, other mediators such as nitric oxide (NO) increase Na excretion. Grapeseed proanthocyanidin extract (GSPE) is a molecule that has an antioxidanteffect by increasing NO levels. Our study was intended to evaluate the ef- fect of GSPE on Na excretion. Material and Method: Fourteen rats were divided into control and GSPE groups. The control group was given 1 cm3milk by gavage for one week, while the GSPE group was given 100 mg/kgGSPE. Seventh-day urines were collected from rats monitored over 24 h ina metabolic cage. Urinary Na excretion at the end of 24 h was investigatedand the experiment concluded. Results: There was no difference between thecontrol and GSPE groups in terms of weight, solid and liquid food intakeand urine volumes. 24-hour urinary Na excretion was higher in the GSPEgroup (1.43±0.30 g/day) compared to the control group (1.37±0.29 g/day),although the difference was not statistically significant. Na excretion waspositively correlated with solid food intake (p=0.029, r=0.583) and urine vol- ume (p

Özet

Amaç: Çeşitli hormon ve aracılar idrar Na atılımını azaltırken nitrik oksid (NO)gibi birtakım aracılar ise Na atılımını arttırmaktadır. Üzüm çekirdeği proant- hocynidin özü (ÜÇPÖ), NO düzeyini arttırarak antioksidan etki eden bir moleküldür. Çalışmamızda ÜÇPÖnin idrar Na atılımı üzerine etkisini değerlendirmeyi amaçladık. Gereç ve Yöntem: 14 adet rat kontrol ve ÜÇPÖ olmak üzere ayrıldı. Kontrol grubuna gavaj ile 1 hafta süreli 1 cm3 süt verilirken ÜÇPÖgrubuna 100mg/kg ÜÇPÖ verildi. 7. gün 24 saat süreli metabolik kafeste takip edilen ratların idrarları toplanıp 24 saatin sonunda idrar Na atılımı çalışıldı ve deney sonlandırıldı. Bulgular: Kontrol ve ÜÇPÖ gruplarının kilo, aldığıkatı ve sıvı gıda ve idrar volumleri arasında fark yoktu. 24 saatlik idrar Na atılımı ÜÇPÖ grubunda (1.43±0.30 gr/gün) kontrol grubuna (1.37±0.29 gr/gün)göre daha fazla idi ancak istatistiksel anlamlı değildi. Na atılımı ile katı gıdaalımı (p=0.029, r=0.583) ve idrar hacimleri (p

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Cite This Article

ALKANAT, M., ULUSOY, Ş., ÖREM, A., ÖZKAN, G., BALABAN, F. Y. (2022). Üzüm Çekirdeği Proanthocyanidin Özü (ÜÇPÖ) nün İdrar Sodyum Atılımı Üzerine Etkisi. Journal of Clinical and Analytical Medicine, Cilt: 5 - Sayı: 6, 469–471. https://ajindex.com/articles/561169

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References (12)

  1. Bełtowski J. Leptin and the Regulation of Renal Sodium Handling and Renal Na-Transporting ATPases: Role in the Pathogenesis of Arterial Hypertension. Curr Cardiol Rev 2010;6(1):31-40
  2. Meneton P, Jeunemaitre X, de Wardener HE, MacGregor GA. Links between dietary salt intake, renal salt handling, blood pressure, and cardiovascular diseases. Physiol Rev 2005;85(2):679-715
  3. Féraille E, Doucet A. Sodium-potassium-adenosinetriphosphatase-dependent sodium transport in the kidney: hormonal control. Physiol Rev 2001;81(1):345- 418
  4. Bagchi D, Sen CK, Ray SD, Das DK, Bagchi M, Preuss HG, et al. Molecular mechanisms of cardioprotection by a novel grape seed proanthocyanidin extract. Mutat Res 2003;523-4:87-97 5. Bagchi D, Bagchi M, Stohs S, Ray SD, Sen CK, Preuss HG. Cellular protection with proanthocyanidins derived from grape seeds. Ann N Y Acad Sci. 2002;957:260-70
  5. Ulusoy S, Ozkan G, Ersoz S, Orem A, Alkanat M, Yucesan FB, et al. The effect of grape seed proanthocyanidin extract in preventing amikacin-induced nephro- pathy. Ren Fail 2012;34(2):227-34
  6. Ozkan G, Ulusoy S, Orem A, Ersoz S, Alkanat M, Yucesan FB, et al. Protective Effect of the Grape Seed Proanthocyanidin Extract in a Rat Model of Contrast- Induced Nephropathy. Kidney Blood Press Res 2012;35(6):445-53
  7. Ulusoy S, Ozkan G, Yucesan FB, et al. Anti-apoptotic and anti-oxidant effects of grape seed proanthocyanidin extract in preventing cyclosporine A-induced neph- ropathy. Nephrology (Carlton) 2012;17(4):372-9
  8. Ozkan G, Ulusoy S, Alkanat M, Orem A, Akcan B, Ersöz S, et al. Antiapoptotic and antioxidant effects of GSPE in preventing cyclosporine A-induced cardiotoxi- city. Ren Fail 2012;34(4):460-6
  9. Cui X, Liu X, Feng H, Zhao S, Gao H. GSPE enhance eNOS expression thro- ugh AMPK/SIRT1-KLF2 pathway and modulate blood pressure in ouabain induced hypertensive rats. Biol Pharm Bull 2012;35(12):2192-7
  10. Magyar CE, Zhang Y, Holstein-Rathlou NH, McDonough AA. Proximal tubule Na transporter responses are the same during acute and chronic hypertension. Am J Physiol Renal Physiol 2000;279(2):358-69
  11. Hinojos CA, Doris PA. Altered subcellular distribution of Na+,K+-ATPase in proximal tubules in young spontaneously hypertensive rats. Hypertension 2004;44(1):95-100
  12. Bagchi D, Garg A, Krohn RL, Bagchi M, Tran MX, Stohs SJ. Oxygen free radical scavenging abilities of vitamins C and E, and a grape seed proanthocyanidin ext- ract in vitro. Res Commun Mol Pathol Pharmacol 1997;95(2):179-