Epidemiological evidence suggests that flavonoids may play an important role in the decreased risk of chronic diseases associated with a diet rich in plant-derived foods. Flavonoids are also common constituents of plants used in traditional medicine to treat a wide range of diseases. The purpose of this article is to summarize the distribution and biological activities of one of the most common flavonoids: luteolin. This flavonoid and its glycosides are widely distributed in the plant kingdom; they are present in many plant families and have been identified in Bryophyta, Pteridophyta, Pinophyta and Magnoliophyta. Dietary sources of luteolin include, for instance, carrots, peppers, celery, olive oil, peppermint, thyme, rosemary and oregano. Preclinical studies have shown that this flavone possesses a variety of pharmacological activities, including antioxidant, anti-inflammatory, antimicrobial and anticancer activities. The ability of luteolin to inhibit angiogenesis, to induce apoptosis, to prevent carcinogenesis in animal models, to reduce tumor growth in vivo and to sensitize tumor cells to the cytotoxic effects of some anticancer drugs suggests that this flavonoid has cancer chemopreventive and chemotherapeutic potential. Modulation of ROS levels, inhibition of topoisomerases I and II, reduction of NF-kappaB and AP-1 activity, stabilization of p53, and inhibition of PI3K, STAT3, IGF1R and HER2 are possible mechanisms involved in the biological activities of luteolin.

Distribution and biological activities of the flavonoid luteolin.

Mineral Nutrition of Higher Plants, 2nd edition, H. Marschner. Academic Press, London (1995), 889, (ISBN 0-12-473543-6). Price: 29.95 Pound Sterling

Anthocyanins and other flavonoids

Secondary metabolites of fungi from marine habitats.

Antioxidant activity of dulse (Palmaria palmata) extract evaluated in vitro

Litter decomposition, governing nutrient and C cycling, is strongly influenced by the chemical litter quality. In order to determine the interspecific variation in leaf decomposition rates and to understand the chemical basis for such variation, decomposition dynamics of seven common canopy species was investigated over 2 year using the litterbag technique in a subtropical evergreen broad-leaved forest on Okinawa Island, Japan. The species studied are representatives of the vegetation in the study area and differed significantly in their chemical litter quality. Dry mass loss at the end of study varied in the order: Distylium racemosum< Quercus miyagii< Rapanea neriifolia< Symplocos confusa< Castanopsis sieboldii< Schima wallichii< Daphniphyllum glaucescens. All species showed a pattern characterized by a rapid initial decomposition followed by lower rates except for D. glaucescenswhich decomposition rate appeared to be rather constant. In the late phase, decomposition rates were correlated positively to initial N and ash contents and negatively to lignin content, lignin:N, C:N, and C:P ratios. The effects of N and lignin content or lignin:N ratio were stronger than other quality parameters. There was a wide range in patterns of N and P concentrations, from a net accumulation to a rapid loss in decomposition. The correlation between N and P release suggests that N and P dynamics may have influenced each other during litter decomposition. Analysis of initial quality for species showed that the C:P ratios were extremely high (range 1639–3811) but the N:P ratios were from 28 to 56, indicating a likely P-limitation for this forest. Our results suggest that P is an important control of litter decomposition and N and P dynamics.

Decomposition patterns of leaf litter of seven common canopy species in a subtropical forest: N and P dynamics

Three flavonol glycosides from leaves of Myrsine seguinii

Hydroquinone diglycoside acyl esters from the leaves of Myrsine seguinii

Decomposition of typhoon-generated and normal leaf litter and their release patterns for eight nutrient elements were investigated over 3 yr using the litterbag technique in a subtropical evergreen broad-leaved forest on Okinawa Island, Japan. Two common tree species, Castanopsis sieboldii and Schima wallichii, representative of the vegetation and differing in their foliar traits, were selected. The elements analyzed were N, P, K, Ca, Mg, Na, Al, Fe and Mn. Dry mass loss at the end of study varied in the order: typhoon green leaves > typhoon yellow leaves > normal leaves falling for both species. For the same litter type, Schima decomposed faster than Castanopsis. Dry mass remaining after 2 yr of decomposition was positively correlated with initial C:N and C:P ratios. There was a wide range in patterns of nutrient concentration, from a net accumulation to a rapid loss in decomposition. Leaf litter generated by typhoons decomposed more rapidly than did the normal litter, with rapid losses for N and P. Analysis of initial quality for the different litter types showed that the C:P ratios were extremely high (range 896 − 2467) but the P:N ratios were < 0.05 (range 0.02 − 0.04), indicating a likely P-limitation for this forest. On average 32% less N and 60% less P was retranslocated from the typhoon-generated green leaves than from the normal litter for the two species, Castanopsis and Schima. An estimated 2.13 g m–2 yr–1 more N and 0.07 g m–2 yr–1 more P was transferred to the soil as result of typhoon disturbances, which were as high as 52% of N and 74% of P inputted from leaf litter annually in a normal year. Typhoon-driven maintenance of rapid P cycling appears to be an important mechanism by which growth of this Okinawan subtropical forest is maintained.

Leaf litter decomposition and nutrient dynamics in a subtropical forest after typhoon disturbance

Extensive isolation work on the n-BuOH-soluble fraction obtained from the leaves of Premna subscandens, collected on Ishigaki island, Okinawa, afforded six compounds. Two were identified as megastigmane glucosides, 7-(3,5-dihydroxy-1,1,5-trimethylcyclohexylidene)-9-methylprop++ +-8-enyl 9-O-beta-D-glucopyranoside and 3-hydroxy-5,6-epoxy-beta-ionol 9-O-beta-D-glucopyranoside. The structures of the remaining four new compounds were elucidated to be a 2'-O-beta-D-apiofuranosyl derivative of 3-hydroxy-5,6-epoxy-beta-ionol 9-O-beta-D-glucopyranoside, named premnaionoside, benzyl alcohol beta-D-(2'-O-beta-D-xylopyranosyl)glucopyranoside, phenethyl alcohol beta-D-(2'-O-beta-D-glucopyranosyl)glucopyranoside, and 4,4'-dimethoxy-beta-truxinic acid catalpol diester by spectroscopic analyses.

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Megastigmane, Benzyl and Phenethyl Alcohol Glycosides, and 4, 4'-Dimethoxy-β-truxinic Acid Catalpol Diester from the Leaves of Premna subscandens MERR.

Eiji Hirata

Papers

Decomposition patterns of leaf litter of seven common canopy species in a subtropical forest: N and P dynamics

Three flavonol glycosides from leaves of Myrsine seguinii

Hydroquinone diglycoside acyl esters from the leaves of Myrsine seguinii

Leaf litter decomposition and nutrient dynamics in a subtropical forest after typhoon disturbance

Megastigmane, Benzyl and Phenethyl Alcohol Glycosides, and 4, 4'-Dimethoxy-β-truxinic Acid Catalpol Diester from the Leaves of Premna subscandens MERR.