Abstract
Cecropia peltata is popularly known as “guarumbo” in Mexico and is used in traditional medicine for treatment of diabetes mellitus. C. peltata plants were cultivated in a hydroponic system under controlled conditions. Gradients of light (20, 30 and 100 μmol m−2 s−1) and nitrate concentrations (13, 2 and 0.2 mM) were applied to estimate their effect on biomass allocation and accumulation of bioactive (chlorogenic acid and isoorientin) phenolic compounds over a 28-day period. According to carbon nutrient balance (CNB) hypothesis predictions, biomass accumulation in foliage was stimulated by the highest irradiance (100 μmol m−2 s−1); similarly, at highest irradiance in combination with lowest nitrate concentration (0.2 mM), root growth was stimulated (root-to-shoot ratio increased twofold with respect to the control). In these conditions, total phenolics (TP) and chlorogenic acid (CGA) contents were higher in aerial parts than in roots, with a 3.8-fold increase in TP and a 7.7-fold increase in CGA in foliage with respect to the control plants. Isoorientin was accumulated at very low levels. Antioxidant activity and total phenolic content showed a strong positive correlation. Phenylalanine ammonia-lyase activity (PAL) in aerial parts exhibited significant changes (>twofold) by highest irradiance. C. peltata plants allocate biomass and/or phenolic compounds to compensate the oxidative damage (increase in MDA levels) due to changes in light and nitrate restriction. The results are the basis for the establishment of a system of C. peltata culture in view of the potential use of C. peltata in therapeutic preparations for the treatment of diabetes mellitus.
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Abbreviations
- AA:
-
Antioxidant activity
- CGA:
-
Chlorogenic acid
- CNB:
-
Carbon nutrient balance
- DM:
-
Dry mass
- FM:
-
Fresh mass
- ISO:
-
Isoorientin
- MDA:
-
Malondialdehyde
- PAL:
-
Phenylalanine ammonia-lyase
- ROS:
-
Reactive oxygen species
- RSR:
-
Root-to-shoot ratio
- TBA:
-
Thiobarbituric acid
- TP:
-
Total soluble phenolics
References
Aguilar A, Camacho JR, Chino S, Jácquez P, López ME (1998) Plantas medicinales del herbario del IMSS, su distribución por enfermedades. Instituto Mexicano del Seguro Social y Grupo Roche Syntex de México, México, p 40
Alonso-Castro AJ, Miranda-Torres AC, González-Chávez MM, Salazar-Olivo LA (2008) Cecropia obtusifolia Bertol and its active compound, chlorogenic acid, stimulate 2-NBDglucose uptake in both insulin-sensitive and insulin-resistant 3T3 adipocytes. J Ethnopharmacol 120:458–464
Andrade-Cetto A, Wiedenfeld H (2001) Hypoglycemic effect of Cecropia obtusifolia on streptozotocin diabetic rats. J Ethnopharmacol 78:145–149
Argueta A, Cano L, Asselein L, Rodarte ME (1994) Atlas de las Plantas de la medicina tradicional mexicana. Instituto Nacional Indigenista (INI) II, México, pp 706–707
Armstrong GM, Rice LMR, Wender SH (1970) The effect of nitrogen deficiency on the concentration of caffeoylquinic acids and scopolin in tobacco. Phytochemistry 9:945–948
Bernards MA, Ellis BE (1991) Phenylalanine ammonia-lyase from tomato cell cultures inoculated with Verticillium albo-atrum. Plant Physiol 97:1494–1500
Brennan T, Frenkel C (1977) Involvement of hydrogen peroxide in the regulation of senescence in pear. Plant Physiol 59:411–416
Briskin DP, Gawienowski MC (2001) Differential effects of light and nitrogen on production of hypericins and leaf glands in Hypericum perforatum. Plant Physiol Biochem 39:1075–1081
Briskin DP, Leroy A, Gawienowski M (2000) Influence on the production of hypericins by St John’s wort. Plant Physiol Biochem 38:413–420
Bryant JP, Chapin FS III, Klein DR (1983) Carbon nutrient balance of boreal plants in relation to vertebrate herbivory. Oikos 40:357–368
Cabrera HM (2002) Ecophysiological responses of plants in ecosystems with Mediterranean-like climate and high mountain environments. Rev Chil His Nat 75:625–637
Cai Y, Luo Q, Sun M, Corke H (2004) Antioxidant activity and phenolic compounds of 112 traditional Chinese medicinal plants associated with anticancer. Life Sci 74:2157–2184
Clé C, Hill LM, Niggeweg R, Martin CR, Guisez Y (2008) Modulation of chlorogenic acid biosynthesis in Solanum lycopersicum: consequences for phenolic accumulation and UV-tolerance. Phytochemistry 69:2149–2156
Coviella CE, Stipanovic RD, Trumble JT (2002) Plant allocation to defensive compounds: interactions between elevated CO2 and nitrogen in transgenic cotton plants. J Exp Bot 53(367):323–331
Dixon RA, Paiva NL (1995) Stress induced phenylpropanoids metabolism. Plant Cell 7:1085–1097
Fritz C, Palacios N, Fiel R, Stitt M (2006) Regulation of secondary metabolism by the carbon–nitrogen status in tobacco: nitrate inhibits large sectors of phenylpropanoids metabolism. Plant J 46:553–548
Grace SC, Logan BA (2000) Energy dissipation and radical scavenging by the plant phenylpropanoid pathway. Philos Trans R Soc Lond B Biol Sci 355:1499–1510
Gray DE, Pallardy SG, Garret HE, Rottinghauss GE (2003) Effect of acute drought stress and time of harvest on phytochemistry and dry weight of St. John’s wort leaves and flowers. Planta Med 69:1024–1030
Grechi I, Vivin Ph, Hilbert G, Milin S, Robert T, Gaudillère JP (2007) Effect of light and nitrogen supply on internal C:N balance and control of root-to-shoot biomass allocation in grapevine. Environ Exp Bot 59:139–149
Gutiérrez-Domínguez MA, Betancourt-Aguilar Y (2008) El mercado de plantas medicinales en México: situación actual y perspectivas de desarrollo. http://www.geocities.com/redmexicana/colombia.doc (accessed July 2009)
Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts. I. Kinetic and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198
Hemm MR, Rider SD, Ogas J, Murry DJ, Chapple C (2004) Light induces phenylpropanoids metabolism in Arabidopsis roots. Plant J 38:765–778
Heo HJ, Jun Kim Y, Chung D, Kim D (2007) Antioxidant capacities of individual and combined phenolics in a model system. Food Chem 104:87–92
Herrera-Arellano A, Aguilar-Santamaría L, García-Hernández B, Nicasio-Torres P, Tortoriello J (2004) Clinical trial of Cecropia obtusifolia and Marrubium vulgare leaf extracts on blood glucose and serum lipids in type 2 diabetics. Phytomedicine 11:561–566
Hoagland DR, Arnon DI (1950) The water-culture method for growing plants without soil. Circular 347. University of California Agricultural Experiment Station, Berkeley, pp 1–32
Horton P (2000) Prospects for crop improvement through the genetic manipulation of photosynthesis: morphological and biochemical aspects of light capture. J Exp Bot 51:475–485
Jaakola L, Määttä-Riihinen K, Kärenlampi S, Hohtola A (2004) Activation of flavonoid biosynthesis by solar radiation in bilberry (Vaccinium myrtillus L.) leaves. Planta 218:721–728
Jansen MAK, Hectors K, O’Brien NM, Guisez Y, Potters G (2008) Plant stress and human health: do human consumers benefit from UV-B acclimated crops? Plant Sci 175:449–458
Khan MH, Panda SK (2008) Alterations in root lipid peroxidation and antioxidative responses in two rice cultivars under NaCl-salinity stress. Acta Physiol Plant 30:81–89
Ko FN, Chu CC, Lin CN, Chang CC, Teng CM (1998) Isoorientin-6”-O-glucoside, a water-soluble antioxidant isolated from Gentiana arisanensis. BBA 1389:8190. (Abstract)
Konieczny R, Libik M, Tuleja M, Niewiadomska E, Miszalski Z (2008) Oxidative events during in vitro regeneration of sunflower. Acta Physiol Plant 30:71–79
Kováčik J, Bačkor M (2007) Phenylalanine ammonia-lyase and phenolic compounds in Chamomile tolerance to cadmium and copper excess. Water Air Soil Pollut 185:185–193
Laloi C, Przybyla D, Apel K (2006) A genetic approach towards elucidating the biological activity of different reactive oxygen species in Arabidopsis thaliana. J Exp Bot 57(8):1719–1724
Le Bot J, Bénard C, Robin C, Bourgaud F, Adamowicz S (2009) The ‘trade-off’ between synthesis of primary and secondary compounds in young tomato leaves is altered by nitrate nutrition: experimental evidence and model consistency. J Exp Bot 60(15):4301–4314
Lichtenthaler HK (1987) Chlorophylls and carotenoids: pigments of photosynthetic biomembranes. Methods Enzymol 148:350–382
López-Bucio J, Cruz-Ramírez A, Herrera-Estrella L (2003) The role of nutrient availability in regulating root architecture. Curr Opin Plant Biol 6:280–287
Marcelis LFM, Heuvelink E (2007) Concepts of modeling carbon allocation among plant organs. In: Vos J, Marcelis LFM, Visser PHB, Struik PC, Evers JB (eds) Functional–structural plant modelling in crop production, 1st edn. Springer, Berlin, pp 103–111
McNally DJ, Wurms KV, Labbé C, Quideau S, Bélanger RR (2003) Complex C-glicosyl flavonoid phytoalexins from Cucumis sativus. J Nat Prod 66:1280–1283
Miller AJ, Fan X, Orsel M, Smith SJ, Wells DM (2007) Nitrate transport and signaling. J Exp Bot 58(9):2297–2306
Mosaleeyanon K, Zobayed SMA, Afreen F, Kozai T (2005) Relationships between net photosynthetic rate and secondary metabolite contents in St. John’s wort. Plant Sci 169:523–531
Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol Plant 15:473–497
Nicasio P, Aguilar S, Aranda E, Ortíz S, González M (2005) Hypoglycemic effect and chlorogenic acid content in two Cecropia species. Phytother Res 19:661–664
Nicasio-Torres P, Erazo-Gómez JC, Cruz-Sosa F (2009) In vitro propagation of two antidiabetic species known as guarumbo: Cecropia obtusifolia and Cecropia peltata. Acta Physiol Plant 31(5):905–914
Osuna L, Mora A, Ventura E, Jiménez E, Bazaldúa C, Jiménez A (2008) Micropropagation of Aristolochia elegans (Mast.). J Crop Sci Biotech 10(3):141–146
Palumbo MJ, Putz FE, Talcott ST (2007) Nitrogen and gender effects on the secondary metabolism of yaupon, a caffeine-containing North American holly. Oecologia 151:1–9
Poorter H, Pepin S, Rijkers T, Jong Y, Evans JR, Körner C (2006) Construction costs, chemical composition and payback time of high- and low-irradiance leaves. J Exp Bot 57(2):355–371
Raskin I, Ribnicky DM, Komamytsky S, Ilic N, Poulev A, Borisjuk N, Brinker A, Moreno DA, Ripoll C, Yakoby N, O’Neal JM, Comwell T, Pastor I, Friendler B (2002) Plants and human health in the twenty-first century. Trends Biotechnol 20:522–531
Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, Rice-Evans C (1999) Antioxidant activity applying improved ABTS radical cation decolorization assay. Free Radic Biol Med 26(9/10):1231–1237
Revilla-Monsalve MC, Andrade-Cetto A, Palomino-Garibay MA, Wiedenfeld H, Islas-Andrade S (2007) Hypoglycemic effect of Cecropia obtusifolia Bertol aqueous extract on type 2 diabetic patients. J Ethnopharmacol 111:636–640
Rodríguez de Sotillo DV, Hadley M (2002) Chlorogenic acid modifies plasma and liver concentrations of cholesterol, triacylglycerol, and minerals in (fa/fa) Zucker rats. J Nutr Biochem 13:717–726
Ryser P, Eek L (2000) Consequences of phenotypic plasticity vs. interspecific differences in leaf and root traits for acquisition of aboveground and belowground resources. Am J Bot 87(3):402–411
Sakihama Y, Cohen MF, Grace SC, Yamashi H (2002) Plant phenolic antioxidant and prooxidant activities: phenolics-induced oxidative damage mediated by metals in plants. Toxicology 177:67–80
Silva EM, Souza JNS, Rogez H, Rees JF, Larondelle Y (2007) Antioxidant activities and polyphenolic contents of fifteen selected plant species from the Amazonian region. Food Chem 101:1012–1018
Street RA, Van Staden SJ (2008) South African traditional medicinal plant trade- challenges in regulating quality, safety and efficacy. J Ethnopharmacol 119:705–710
Takei K, Takahashi T, Sugiyama T, Yamaya T, Sakakibara H (2002) Multiple routes communicating nitrogen availability from roots to shoots: a signal transduction pathway mediated by cytokinin. J Exp Bot 53(370):971–977
Tewari RK, Kumar P, Sharma PN (2006) Magnesium deficiency induced oxidative stress and antioxidant responses in mulberry plants. Sci Hortic 108:7–14
Urbanczyk-Wochniak E, Fernie AR (2005) Metabolic profiling reveals altered nitrogen nutrient regimes have diverse effects on the metabolism of hydroponically-grown tomato (Solanum lycopersicum) plants. J Exp Bot 56(410):309–321
Wilson JB (1988) A review of evidence on the control of shoot:root ratio in relation to models. Ann Bot 61:433–449
Winkel-Shirley B (2002) Biosynthesis of flavonoids and effects of stress. Curr Opin Plant Biol 5:218–223
Acknowledgments
This research was partially supported by a scholarship from the Consejo Nacional de Ciencia y Tecnología-México (CONACyT-México) (CVU 42514) and from the Instituto Mexicano del Seguro Social (IMSS) (99183755).
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Communicated by Z.-L. Zhang.
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Mora Izquierdo, A., Nicasio Torres, M.d.P., Sepúlveda Jiménez, G. et al. Changes in biomass allocation and phenolic compounds accumulation due to the effect of light and nitrate supply in Cecropia peltata plants. Acta Physiol Plant 33, 2135–2147 (2011). https://doi.org/10.1007/s11738-011-0753-5
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DOI: https://doi.org/10.1007/s11738-011-0753-5