Influenza and pneumococcal vaccinations in dialysis patients in a London district general hospital.

Background: Patients on dialysis mount reduced immune responses compared with the general population. The Department of Health advises that these patients receive influenza and pneumococcal vaccinations at regular intervals-once yearly and every five years, respectively. This article investigates the uptake of these vaccinations in this patient population and seeks to examine factors that may influence vaccination status such as patient's language and presence of a general practitioner (GP) electronic vaccination reminder system.

Variations in lipophilic and vacuolar flavonoids among European Pulicaria species.

Four European Pulicaria species, P. odora, P. paludosa, P.

Identification of lipophilic flavones and flavonols by comparative HPLC, TLC and UV spectral analysis.

The identification of lipophilic flavones and flavonols using a combination of high performance liquid chromatography, thin layer chromatography and UV spectral analysis is discussed. Data are provided for the flavones, apigenin, luteolin and tricetin and twelve of their methyl ethers, 8-hydroxyluteolin, 6-hydroxyluteolin and scutellarein and fourteen of their methyl ethers, and some 6,8-dihydroxyapigenin and 6,8-dihydroxyluteolin derivatives. Data for some forty two flavonols with extra 6- and/or 8-hydroxylation, mostly 6-hydroxykaempferol and quercetagetin derivatives, are also presented.

Acacetin glycosides as taxonomic markers in Calamintha and Micromeria.

A new acetylated flavone glycoside, acacetin 7-O-[6""-O-acetylglucosyl(1""-->2")]rhamnosyl(1"'-->6")glucoside, has been isolated from the leaves of Calamintha glandulosa together with the known compound acacetin 7-O-rhamnosyl(1"'-->6")glucoside. The occurrence of these flavonoids in the closely related genera Satureja, Micromeria, Acinos and Clinopodium indicates that their distribution may be of taxonomic significance.

The role of lipophilic and polar flavonoids in the classification of temperate members of the Anthemideae.

Lipophilic and vacuolar flavonoids were separately identified in representative temperate species of the genera Anthemis, Chrysanthemum, Cotula, Ismelia, Leucanthemum and Tripleurospermum. The four Anthemis species investigated variously produced four main surface constituents, in leaf and flower: santin, quercetagetin 3,6,3'-trimethyl ether, scutellarein 6,4'-dimethyl ether and 6-hydroxyluteolin 6,3'-dimethyl ether. By contrast, surface extracts of disc and ray florets of the species of Chrysanthemum, Cotula, Ismelia, Leucanthemum and Tripleurospermum surveyed yielded five common flavones in the free state: apigenin, luteolin, acacetin, apigenin 7-methyl ether and chrysoeriol.

A distinctive flavonoid chemistry for the anomalous genus Biebersteinia.

Leaf surface extracts of Biebersteinia orphanidis have yielded a complex mixture of five flavones with the unusual 5,7-dihydroxy-6,8-dimethoxy A ring substitution pattern. They are acerosin, hymenoxin, nevadensin, sudachitin and 5,7,4'-trihydroxy-6,8-dimethoxyflavone. Also present at the leaf surface are gardenin B, luteolin, apigenin, acacetin and the coumarin umbelliferone.

Advances in flavonoid research since 1992.

Some of the recent advances in flavonoid research are reviewed. The role of anthocyanins and flavones in providing stable blue flower colours in the angiosperms is outlined. The contribution of leaf flavonoids to UV-B protection in plants is critically discussed.

Geographical variation in the surface flavonoids of Pulicaria dysenterica.

Four chemical races were detected in Pulicaria dysenterica, when sampled within Europe, on the basis of the surface flavonoids present. One race uniquely contained quercetagetin 3,7-dimethyl ether and another 6-hydroxykaempferol 3,4'-dimethyl ether. A third race was based on plants having 6-hydroxykaempferol 3,7-dimethyl ether together with quercetagetin 3,7,3'-trimethyl ether.

The flavonoids of Tanacetum parthenium and T. vulgare and their anti-inflammatory properties.

The lipophilic flavonoids in leaf and flower of Tanacetum parthenium and T. vulgaris have been compared. While those of T.

Condensed tannins and sugars in the diet of chimpanzees (Pan troglodytes schweinfurthii) in the Budongo Forest, Uganda.

Fruits, leaves and bark forming part of the diet of chimpanzees were collected and it was noted whether samples were of a kind being eaten or not eaten. Samples were dried and analysed for condensed tannin content and for three sugars, glucose, sucrose and fructose. It was found that chimpanzees did not select foods according to the level of tannins but did so according to the levels of sugars, preferring the higher levels.

Chrysin and other leaf exudate flavonoids in the genus Pelargonium.

In a chemotaxonomic survey of 57 Pelargonium species, leaf exudate flavonoids were detected in 35% of the sample, mostly in trace amounts. However, chrysin and a related C-methylflavanone were identified as major leaf surface constituents of P. crispum, and a mixture of quercetin and kaempferol mono-, and di- and trimethyl ethers of P.

A biologically active lipophilic flavonol from Tanacetum parthenium.

A new lipophilic flavonol, 6-hydroxykaempferol 3,7,4'-trimethyl ether, called tanetin, has been characterized in the leaf, flower and seed of feverfew, Tanacetum parthenium. It co-occurs with the known 6-hydroxykaempferol 3,7-dimethyl ether, quercetagetin 3,7-dimethyl ether and quercetagetin 3,7,3'-trimethyl ether. Pharmacological tests indicate that tanetin could contribute to the anti-inflammatory properties of feverfew by inhibiting the generation of pro-inflammatory eicosanoids, although it is unlikely to be the only biologically active compound within the plant.

Methylated C-glycosylflavones as taxonomic markers in orchids of the subtribe Ornithocephalinae.

In a leaf flavonoid survey of 15 Brazilian orchid species from the subtribe Ornithocephalinae, flavone C-glycosides were found to be the major constituents in all except two Ornithocephalus taxa. In Zygostates cornuta a rare glycoside, apigenin 7,4'-dimethyl ether 6-C-glucoside-2"-O-rhamnoside, was identified. This also occurred in Z.

Role of secondary metabolites in chemical defence mechanisms in plants.

The classic view that secondary constituents are waste products in plants has been replaced by one in which their value is assumed to be as a protection against herbivorous and microbial attack. However, secondary pathways may still be physiologically important as a means of channelling and storing carbon compounds, accumulated from photosynthesis, during periods when nitrogen is limiting or whenever leaf growth is curtailed. Large increases in the amount of secondary metabolites can occur in stressed plants and those subject to mechanical damage or that caused by insects.