Antioxidant activity of Trifolium resupinatum L. exposed to different extracts from leaves, flowers and shoots of Prangos ferulacea

  • Mohsen Bazdar Shiraz University, College of Agriculture, Dept. Natural Resources and Environmental Engineering. 71441-65186 Shiraz
  • Hossein Sadeghi Shiraz University, College of Agriculture, Dept. Natural Resources and Environmental Engineering. 71441-65186 Shiraz
Keywords: superoxide dismutase, peroxidase, lipid peroxidation, hydrogen peroxide

Abstract

Prangos ferulacea is a member of Apiaceae family, is a popular fodder for livestock production and an important species in rangeland restoration. The objectives of the research are the comparative phytotoxic activity of aqueous and hydroalcoholic extracts obtained from different organs (flower, shoot and leaf) of P. ferulacea on antioxidant response of Trifolium resupinatum was investigated in a laboratory bioassay. Antioxidant enzyme activities including catalase (CAT), peroxidase (POD), ascorbic peroxidase (APX), and superoxide dismutase (SOD), in line with content of malondialdehyde (MDA) and hydrogen peroxide were measured. Results indicated that hydroalcoholic extract of P. ferulaceae flower possess the highest total phenolic content as well as highest phytotoxic effect on T. resupinatum. The highest antioxidant enzyme activity belonged to hydroalcoholic treatment. The treated T. resupinatum seedlings experienced lipid peroxidation at high extract concentrations (12% of hydroalcoholic and 100% of aqueous extract) as evidenced by increased concentration of MDA. In response to this, the activities of SOD, CAT, POD and APX increased at lower extract concentrations but significantly dropped as concentrations increased. According to results of this study, rehabilitation of T. resupinatum sites through the use of P. ferulaceae will probably not be successful.

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Author Biography

Hossein Sadeghi, Shiraz University, College of Agriculture, Dept. Natural Resources and Environmental Engineering. 71441-65186 Shiraz

References

Ahmed J, Guvence A, Kucuboyaci N, Baldemir A, Coskun M, 2011. Total phenolic contents and antioxidant activities of Prangos Lindl. (Umbelliferae) species growing in Konya province (Turkey). Turk J Biol 35: 353-360.

Azarfard F, 2008. Effect of Prangos ferulacea replacement for alfalfa on growth performance and carcass characteristics of Lori lambs. Int J Agric Biol 10 (2): 224-226.

Batish DR, Singh HP, Setia N, Kaur S, Kohli RK, 2006. 2-Benzoxazolinone (BOA) induced oxidative stress, lipid peroxidation and changes in some antioxidant enzyme activities in mung bean (Phaseolus aureus). Plant Physiol Biochem 44: 819-827. https://doi.org/10.1016/j.plaphy.2006.10.014

Chance M, Maehly AC, 1955. Assay of catalases and peroxidases. Methods Enzymol 2: 764-817. https://doi.org/10.1016/S0076-6879(55)02300-8

Correa LR, Soares GLC, Fett-Neto AG, 2008. Allelopathic potential of Psychotoria leiocarpa, a dominant understorey species of subtropical forests. S Afr J Bot 74: 583-590. https://doi.org/10.1016/j.sajb.2008.02.006

Coskun B, Gulsen N, Umucalilar HD, 2004.The nutritive value of Prangos ferulacea. Grass Forage Sci 59 (1): 15-19. https://doi.org/10.1111/j.1365-2494.2004.00398.x

Cruz-Ortega R, Ayala-Cordero G, Anaya AL, 2002. Allelochemical stress produced by the aqueous leachate of Callicarpa acuminata: Effects on roots of bean, maize and tomato. Physiol Plant 116: 20-27. https://doi.org/10.1034/j.1399-3054.2002.1160103.x

Eilami B, 2008. Substitution of alfalfa hay with prangos ferulacea in the fattening diet of gray shirazy sheep. Pajouhesh-Va-Sazandegi 79: 52-57 [In Persian].

Giannopolitis CN, Ries SK, 1977. Superoxide dismutase. I. Occurrence in higher plants. Plant Physiol 59: 309-314. https://doi.org/10.1104/pp.59.2.309

Gill SS, Toteja N, 2010. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem 48: 909-930. https://doi.org/10.1016/j.plaphy.2010.08.016

Heath RL, Packer L, 1968. Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arc Biochem Biophysics 125: 189-198. https://doi.org/10.1016/0003-9861(68)90654-1

Ibañez J, Martinez J, Schnabel S, 2007. Desertification due to overgrazing in a dynamic commercial livestock-grass-soil system. Ecol Model 205: 277-288. https://doi.org/10.1016/j.ecolmodel.2007.02.024

Iranian Nomadic Organization, 1992. Iranian Nomadic Organization. Proc Development Strategy of Iranian Nomadic Life, Ashayeri Publications, Iran, 34 pp.

Kaur S, Singh HP, Batish DR, Kohli RK, 2012. Artemisia scoparia essential oil inhibited root growth involves reactive oxygen species (ROS)-mediated disruption of oxidative metabolism: In vivo ROS detection and alterations in antioxidant enzymes. Biochem Sys Ecol 44: 390-399. https://doi.org/10.1016/j.bse.2012.06.015

Orozco-Cadenas ML, Narvaez-Vasquez J, Ryan CA, 2001. Hydrogen peroxide acts as a second messenger for the induction of defense genes in tomato plants in response to wounding, systemin, and methyl jasmonate. Plant Cell 13: 179-191. https://doi.org/10.1105/tpc.13.1.179

Palmer MA, Ambrose RF, Poff NL, 1997. Ecological theory and community restoration ecology. Restor Ecol 5: 291-300. https://doi.org/10.1046/j.1526-100X.1997.00543.x

Razavi SM, 2012. Chemical composition and some allelopathic aspects of essential oils of (Prangos ferulacea L.) Lindl at different stages of growth. J Agric Sci Tech 14 (2): 349-56.

Romero-Romero, Sánchez-Nieto T, SanJuan-Badillo S, Anaya A, Cruz-Ortega R, 2005. Comparative effects of allelochemical and water stress in roots of Lycopersicon esculentum Mill. (Solanaceae), Plant Sci 168: 1059-1066. https://doi.org/10.1016/j.plantsci.2004.12.002

Sadeghi S, Robati Z, 2015. Response of Cichorium intybus L. to eight seed priming methods under osmotic stress conditions. Biocatal Agric Biotechnol 4: 443-448. https://doi.org/10.1016/j.bcab.2015.08.003

Salam MA, Noguchi HK, 2010. Allelopathic potential of methanol extract of Bangladesh rice seedlings. Asian J Crop Sci 2: 70-77. https://doi.org/10.3923/ajcs.2010.70.77

SAS Inst., 2004. SAS/STAT 9.1.3. User's Guide. SAS Publishing, SAS Institute Inc., Cary, NC, USA.

Singh HP, Batish DR, Kaur S, Arora K, Kohli RK, 2006. α-Pinene inhibits growth and induces oxidative stress in roots. Annals Bot 98: 1261-1269. https://doi.org/10.1093/aob/mcl213

Singh S, Prasad SM, 2014. Growth, photosynthesis and oxidative responses of Solanum melongena L. seedlings to cadmium stress: Mechanism of toxicity amelioration by kinetin. Sci Hortic 176: 1-10. https://doi.org/10.1016/j.scienta.2014.06.022

Sunmonu TO, Van Staden J, 2014. Phytotoxicity evaluation of six fast-growing tree species in South Africa. S Afr J Bot 90: 101-106. https://doi.org/10.1016/j.sajb.2013.10.010

Tawaha K, Alali FQ, Gharaibeh M, Mohammad M, El-Elimat T, 2007. Antioxidant activity and total phenolic content of selected Jordanian plant species. Food Chem 104: 1372-1378. https://doi.org/10.1016/j.foodchem.2007.01.064

Tiffany L, Park S, Vivanco GM, 2004. Biochemical and physiological mechanisms mediated by alleochemicals. Curr Opin Plant Biol 7: 472-479. https://doi.org/10.1016/j.pbi.2004.05.007

Zhang RM, Zou ZJ, Gao PJ, Hou P, Wen GS, Gao Y, 2012. Allelopathic effects of VOCs of Artemisia frigida Willd. on the regeneration of pasture grasses in Inner Mongolia. J Arid Environ 87: 212-218. https://doi.org/10.1016/j.jaridenv.2012.04.008

Zhu Z, Wei G, Li J, Qian Q, Yu J, 2004. Silicon alleviates salt stress and increases antioxidant enzymes activity in leaves of salt-stressed cucumber (Cucumis sativus L). Plant Sci 167: 527-533. https://doi.org/10.1016/j.plantsci.2004.04.020

Published
2018-02-07
How to Cite
Bazdar, M., & Sadeghi, H. (2018). Antioxidant activity of Trifolium resupinatum L. exposed to different extracts from leaves, flowers and shoots of Prangos ferulacea. Spanish Journal of Agricultural Research, 15(4), e0303. https://doi.org/10.5424/sjar/2017154-10779
Section
Agricultural environment and ecology