Acute and Sub-Acute Oral Toxicity Profile of Purified Tomato Extract on the Liver and Kidney Functions of Male Wistar Rats

doi.org/10.26538/tjnpr/v5i11.12

Authors

  • Ni K. Warditiani Department of Pharmacy, Mathematics and Natural Science Faculty, Udayana University, Indonesia
  • Pande M.N.A. Sari Department of Pharmacy, Mathematics and Natural Science Faculty, Udayana University, Indonesia
  • Putu S. Yustiantara Department of Pharmacy, Mathematics and Natural Science Faculty, Udayana University, Indonesia
  • I-Made A.G. Wirasuta Department of Pharmacy, Mathematics and Natural Science Faculty, Udayana University, Indonesia

Keywords:

Acute toxicity, Lycopene, Purified tomato extract (PTE), Sub-chronic toxicity, Tomato

Abstract

The pharmacological properties of lycopene-containing extracts are numerous. Purified tomato extract (PTE) is a lycopene-rich extract with a wide range of pharmacological properties; however, toxicity testing is required to examine the potential risks associated with the constituent chemicals. This study was conducted to evaluate the acute and sub-chronic toxicities of PTE on the liver and kidney functions of Wistar rats. PTE was obtained by extracting tomatoes using a solvent mixture of n-hexane: acetone: ethanol (1:1:2) and the solvent was then evaporated. For the acute toxicity testing, the rats were divided into two groups: normal control and PTE (750 mg/kg b.w.) treatment groups. The rats were observed for seven days for bodyweight and physiological changes (stool, activity, tremor, and coma), as well as death. In the sub-chronic toxicity testing, the rats were divided into five groups: normal control, PTE (50, 100, or 150 mg/kg b.w.) treatment, and negative control groups. The rats were observed for 28 days for bodyweight changes. Also, the serum urea, creatinine, aminotransferase, aspartate aminotransferase levels were determined. There were no significant differences in the body weight between the normal control and PTE treatment groups, which were 182.85 ± 6.36 g and 184.28 ± 6.72 g, respectively. A similar result was obtained for the physiological conditions which included normal stool, principal activity, no tremor, no coma, as well as no deaths in both groups. The sub-chronic study results showed that PTE was safe. The administration of a single dose of PTE for 28 days did not cause any damage. 

References

Food and Drug Supervisory Agency of the Republic of Indonesia, Regulation of the Head of the Food and Drug Supervisory Agency of the Republic of Indonesia. Number 7 of 2014 concerning Guidelines for In Vivo Nonclinical Toxicity Testing, Jakarta, Indonesia, 2014.

Imran M, Ghorat F, Ul-Haq I, Ur-Rehman H, Aslam F, Heydari M, Shariati MA, Okuskhanova E, Yessimbekov Z, Thiruvengadam M, Hashempur MH, Rebezov M. Lycopene as a natural antioxidant used to prevent human health disorders. Antioxidants. 2020; 9(8):706-733.

Alvi SS, Ansari IA, Khan I, Iqbal J, Khan MS. Potential role of lycopene in targeting proprotein convertase subtilis in kexin type-9 to combat hypercholesterolemia. Free Radic Biol Med. 2017; 108(4):394-403.

Domínguez R, Gullón P, Pateiro M, Munekata PES, Zhang W, Lorenzo JM. Tomato as Potential Source of Natural Additives for Meat Industry. A Review. Antioxidants. 2020; 9(1):73-95.

Warditiani NK, Sari PMNA, Wirasuta IMAG. Phytochemical and hypoglycemia effect of tomato lycopene extract (TLE). Sys Rev Pharm. 2020; 11(4):509-514.

Warditiani NK, Arisanti CIS, Wirasuta IMAG. Antidyslipidemia activity of tomato extract in Wistar male albino rats induced fat-rich-diet and dexamethasone. J Pharm Sci Res. 2019; 11(7):2684-2688.

Warditiani NK, Sari PMNA, Ramona Y, Wirasuta MIAG. The potential of carotene compound (Beta-carotene and lycopene) in steamed tomatoes extract as atherosclerosis preventive nutraceuticals. Trop J Nat Prod Res. 2021; 5(5):889-894.

Honda M, Higashiura T, Fukaya T. Safety assessment of a natural tomato oleoresin containing high amounts of Zisomers of lycopene prepared with supercritical carbon dioxide. J Sci Food Agric. 2016; 97(3):1027-1033.

Jamshidzadeh A, Baghban M, Azarpira N, Bardbori AM, Niknahad H. Effects of tomato extract on oxidative stress induced toxicity in different organs of rats. Food Chem Toxicol. 2008; 46(12):3612-3615.

Gatsing D, Aliyu RR, Kuiate JR, Garba IH, Jaryum KH, Tedongmo N, Toxicological evaluation of aqueous extract of Allium sativum bulbs on laboratory mice and rats. Cameroon J Exp Biol. 2005; 1(1):39-45.

Ulican O, Greksak M, Vancova O, Zlatos L, Galbavý S, Bozek P, Nakano M. Hepatoprotective effect of rooibos tea (Aspalathus linearis) on CCl4-induced liver damage in rats. Physiol Res. 2003; 52(4):461-466.

Porchezhian E and Ansari HS. Hepatoprotective effect of Abutilon indicum on experimental liver damage in rats. Phytomed. 2005; 12(1):62-64.

Uchendu KI, Agu EC, Orji CO. Effect of tomato (Lycopersicon esculentum) extract on acetaminopheninduced acute hepatotoxicity in albino Wistar rat. BEBA. 2018; 2(1):1-70.

Ackay A, Turkmen K, Lee D. Update on the diagnosis and management of acute kidney injury. Int J Nephrol Renovasc Dis. 2010; 3(9):129-140.

Lee KJ, Lee GA, Ma KH, Raveendar S, Cho YH, Lee JR, Chun JW. Chemical constitutions and antioxidant activities of tomato leaf extracts. Plant Breed Biotech. 2016; 4(3):362-372.

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Published

2021-11-01

How to Cite

K. Warditiani, N., M.N.A. Sari, P., S. Yustiantara, P., & A.G. Wirasuta, I.-M. (2021). Acute and Sub-Acute Oral Toxicity Profile of Purified Tomato Extract on the Liver and Kidney Functions of Male Wistar Rats: doi.org/10.26538/tjnpr/v5i11.12. Tropical Journal of Natural Product Research (TJNPR), 5(11), 1962–1965. Retrieved from https://tjnpr.org/index.php/home/article/view/318