Journals / Turkish Journal of Biology / 2012 / Cilt: 36 - Sayı: 1

Protective effects of b-carotene and silymarin on human lymphocytes

Pages
47–52
Publication Date
2012-01-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

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

The data presented here provide a comparative, preliminary insight into the protective role of both b-carotene and silymarin on L-arginine-induced genotoxicity in in vitro lymphocyte cultures.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Beta-carotene and silymarin have antioxidant properties against oxidative damage and are used as dietary supplements.
📊
Key Findings & Data:Study samples were lymphocyte cultures set up from venous blood obtained from 6 healthy individuals (3 males and 3 females).
💡
Conclusion & Impact:The data presented here provide a comparative, preliminary insight into the protective role of both b-carotene and silymarin on L-arginine-induced genotoxicity in in vitro lymphocyte cultures.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Key words: L-arginine · b-carotene · silymarin

Abstract

Beta-carotene and silymarin have antioxidant properties against oxidative damage and are used as dietary supplements. The aim of this study was to assess the protective effects of b-carotene and silymarin on healthy human lymphocytes exposed to L-arginine-induced oxidative damage. Study samples were lymphocyte cultures set up from venous blood obtained from 6 healthy individuals (3 males and 3 females). Oxidative DNA damage was induced by L-arginine. b-Carotene and silymarin were added to the cultures as antioxidants to observe their protective effects, if any. Alkaline single-cell gel electrophoresis (SCGE) was used to evaluate DNA damage. While L-arginine generated genotoxic damage in the lymphocyte cultures, both b-carotene and silymarin had positive effects on the reversal of the induced genotoxicity. When b-carotene was applied in combination with silymarin, there was no significant change in mean tail moments in comparison to the use of b-carotene or silymarin alone. The data presented here provide a comparative, preliminary insight into the protective role of both b-carotene and silymarin on L-arginine-induced genotoxicity in in vitro lymphocyte cultures.

Özet

Beta-carotene and silymarin have antioxidant properties against oxidative damage and are used as dietary supplements. The aim of this study was to assess the protective effects of b-carotene and silymarin on healthy human lymphocytes exposed to L-arginine-induced oxidative damage. Study samples were lymphocyte cultures set up from venous blood obtained from 6 healthy individuals (3 males and 3 females). Oxidative DNA damage was induced by L-arginine. b-Carotene and silymarin were added to the cultures as antioxidants to observe their protective effects, if any. Alkaline single-cell gel electrophoresis (SCGE) was used to evaluate DNA damage. While L-arginine generated genotoxic damage in the lymphocyte cultures, both b-carotene and silymarin had positive effects on the reversal of the induced genotoxicity. When b-carotene was applied in combination with silymarin, there was no significant change in mean tail moments in comparison to the use of b-carotene or silymarin alone. The data presented here provide a comparative, preliminary insight into the protective role of both b-carotene and silymarin on L-arginine-induced genotoxicity in in vitro lymphocyte cultures.

🔖

Cite This Article

YURTCU, E., KASAPOĞLU, E., ŞAHİN, F. İ. (2012). Protective effects of b-carotene and silymarin on human lymphocytes. Turkish Journal of Biology, Cilt: 36 - Sayı: 1, 47–52. https://ajindex.com/articles/182402

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (9)

  1. Zhang P, Omaye ST. DNA strand breakage and oxygen tension: eff ects of beta-carotene, alpha-tocopherol and ascorbic acid. Food Chem Toxicol 39: 239-246, 2001. 2. Sies H, Stahl W. Vitamins E and C, beta-carotene, and other carotenoids as antioxidants. Am J Clin Nutr 62: 1315S-1321S, 1995. 3. Ray SD, Lam TS, Rotollo JA et al. Oxidative stress is the master operator of drug and chemically-induced programmed and unprogrammed cell death: Implications of natural antioxidants in vivo. Biofactors 21: 223-232, 2004.
  2. Orhan İ, Özçelik B, Şener B. Evaluation of antibacterial, antifungal, antiviral, and antioxidant potentials of some edible oils and their fatty acid profi les. Turk J Biol 35: 251-258, 2011.
  3. Ansari MA, Keller JN, Scheff SW. Protective eff ect of Pycnogenol in human neuroblastoma SH-SY5Y cells following acrolein-induced cytotoxicity. Free Radic Biol Med 45: 1510- 1519, 2008. 6. Krinsky NI, Johnson EJ. Carotenoid actions and their relation to health and disease. Mol Aspects Med 26: 459-516, 2005.
  4. Comelli MC, Mengs U, Schneider C et al. Toward the defi nition of the mechanism of action of silymarin: activities related to cellular protection from toxic damage induced by chemotherapy. Integr Cancer Th er 6: 120-129, 2007. 8. Post-White J, Ladas EJ, Kelly KM. Advances in the use of milk thistle (Silybum marianum). Integr Cancer Th er 6: 104-109, 2007. 9. Ladas EJ, Kelly KM. Milk thistle: is there a role for its use as an adjunct therapy in patients with cancer? J Altern Complement Med 9: 411-416, 2003.
  5. Cemek M, Enginar H, Karaca T et al. In vivo radioprotective eff ects of Nigella sativa L oil and reduced glutathione against irradiation-induced oxidative injury and number of peripheral blood lymphocytes in rats. Photochem Photobiol 82: 1691- 1696, 2006.
  6. Erden CD, Ekmekci A, Sahin FI et al. L-arginine and mitomycin C-induced nitric oxide release and apoptosis in human lymphocytes. Cell Biol Int 27: 337-340, 2003.
  7. Bal F, Sahin FI, Yirmibes M et al. Th e in vitro eff ect of beta- carotene and mitomycin C on SCE frequency in Down’s syndrome lymphocyte cultures. Tohoku J Exp Med 184: 295- 300, 1998.
  8. Yilmaz Z, Karabay G, Oktem M et al. Th e apoptotic eff ects of mitomycin C on human endometrial cell cultures and reversal of its eff ects by beta-carotene and folic acid. Acta Physiol Hung 93: 41-51, 2006.
  9. Micozzi MS, Brown ED, Edwards BC et al. Plasma carotenoid response to chronic intake of selected foods and β-carotene supplements in men. Am J Clin Nutr 55: 1120-11