The role of flavor and fragrance chemicals in TRPA1 (transient receptor potential cation channel, member A1) activity associated with allergies

TRPA1 has been proposed to be associated with diverse sensory allergic reactions, including thermal (cold) nociception, hearing and allergic inflammatory conditions. Some naturally occurring compounds are known to activate TRPA1 by forming a Michael addition product with a cysteine residue of TRPA1 through covalent protein modification and, in consequence, to cause allergic reactions. The anti-allergic property of TRPA1 agonists may be due to the activation and subsequent desensitization of TRPA1 expressed in sensory neurons. In this review, naturally occurring TRPA1 antagonists, such as camphor, 1,8-cineole, menthol, borneol, fenchyl alcohol and 2-methylisoborneol, and TRPA1 agonists, including thymol, carvacrol, 1’S-1’- acetoxychavicol acetate, cinnamaldehyde, α-n-hexyl cinnamic aldehyde and thymoquinone as well as isothiocyanates and sulfides are discussed

Seasonal variation in essential oil composition, oil toxicity and the biological activity of solvent extracts of three South African Salvia species

Aromatic plants contain both volatile and non-volatile fractions and the chemical composition of these two fractions may be influenced by seasonal changes. The essential oil and solvent extracts of S. africana-caerulea, S. africana-lutea and S. lanceolata, collected at the same locality throughout the 2005 growing season, were compared in terms of essential oil composition, yields and biological activities. Mostly quantitative, rather than qualitative variationwas observed in the oil composition of each species.Major fluctuations in the composition of S. africana-caerulea oil included limonene (2–33%) and viridiflorol (2–24%). Levels of α-pinene (1–12%), myrcene (2–12%) and α-eusdesmol (trace-13%) fluctuated seasonally in the S. africana-lutea oil. In S. lanceolata, considerable changeswere noted for β-caryophyllene (1–19%), β-caryophyllene oxide (1–21%) and ledol (3–12%). The extract prepared from S. lanceolata harvested inwinterwas more active against Gram-positive bacteria. The S. africana-caerulea extract exhibited the most favourable antiplasmodial activity when harvested in winter (IC50 value: 12 μgml−1), which contrasts with the lowest anti-plasmodial activity of S. lanceolata obtained at the same period (IC50 value: 43 μgml−1). The anti-oxidant activity of the solvent extracts also displayed variation over seasons with thewinter collection of S. africana-lutea yielding the most favourable anti-oxidant activity (IC50 value: 10 μg ml−1). All the solvent extracts prepared from the winter collection exhibited the lowest toxicity (20bIC50 valuesb60 μg ml−1), while the three essential oils obtained from autumn collection were more toxic (0.03bIC50 valuesb0.4 μg ml−1)

Morphological characterisation and agronomical parameters of different species of Salvia sp. (Lamiaceae)

The aim of this work is to assess the morphological characteristics and parameters of biomass production, such as fresh and dry matter weight (FMW and DMW, g/plant), yield of dry matter (YDM) in terms of ton/ha, essential oil content (EOC, mL/100 g) and yield of essential oils (YEO) expressed as L/ha of the following plants Salvia verbenaca, Salvia argentea, Salvia lavandulifolia, Salvia pratensis, Salvia sclarea, Salvia triloba and Salvia officinalis. Except for Salvia argentea (S2) all other species have adapted to the south Brazilian climate conditions, with morphological differences among the species evaluated. In terms of DMW and YDM, S. officinalis was found to be the most productive species with 445.83 g/plant and 11.14 ton/ha. The higher essential oil content and yield was observed for S. officinalis, affording 1.99 mL/100 g and 221.74 L/ha, respectively. Chemical characterisation of the essential oils obtained from hydrodistillation was performed through GC and GC/MSD analyses, which revealed for most of the species studied, α e β-thujone, camphor and 1,8-cineole as major compounds, apart from S. sclarea, for which linalool, linalyl acetate and α-terpineol were the major components