Spiranthera odoratissima A. St. Hil. (manacá) is used in folk medicine to treat renal and hepatic diseases, stomachache, headaches and rheumatism. A central nervous system (CNS) depressant effect of the hexane fraction from the ethanolic extract of this plant has been described. β-caryophyllene, the main component of this essential oil, is a sesquiterpene compound with anti-inflammatory properties that has been found in essential oils derived from several medicinal plants. This work is aimed to evaluate the pharmacological activity of the essential oil obtained from S. odoratissima leaves (EO) and its major component on the murine CNS; we aimed to evaluate a possible anxiolytic-like effect and the underlying mechanisms involved. In an open field test, EO (500 mg/kg) and β-caryophyllene (50, 100 and 200 mg/kg) increased the crossing frequency (P<0.05) and, EO (250 and 500 mg/kg) and β-caryophyllene (200 mg/kg) increased the time spent in the center (P<0.05) without altering total crossings of the open field. EO and β-caryophyllene did not alter the number of falls in the rota-rod test (P>0.05). In the pentobarbital-induced sleep test, EO (500 mg/kg) and β-caryophyllene (200 and 400 mg/kg) decreased the latency to sleep (P<0.05), and EO (125, 250 and 500 mg/kg) (P<0.001) and β-caryophyllene (200 and 400 mg/kg) (P<0.05 and P<0.001) increased the sleep time. In anxiety tests, EO (500 mg/kg) and β-caryophyllene (100 and 200 mg/kg) increased head-dipping behavior (P<0.05) in the hole-board test, entries (P<0.05) into and time spent (P<0.05) on the open arms of the elevated plus maze (EPM), and number of transitions (P<0.05) and time spent in the light compartment (P<0.05) of a light-dark box (LDB). We further investigated the mechanism of action underlying the anxiolytic-like effect of EO and β-caryophyllene by pre-treating animals with antagonists of benzodiazepine (flumazenil) and 5-HT(1A) (NAN-190) receptors prior to evaluation using EPM and LDB. The anxiolytic-like effects of EO were significantly reduced by pre-treatment with NAN-190 (P<0.05) but not flumazenil (P>0.05). The anxiolytic-like effects of β-caryophyllene were not blocked by either NAN-190 or flumazenil (P>0.05). In conclusion, these results suggest that the essential oil derived from S. odoratissima produces an anxiolytic-like effect without altering motor performance and that this effect is mediated by 5-HT(1A) but not via benzodiazepine receptors. In addition, the major component, β-caryophyllene, also has an anxiolytic-like effect that may contribute to the effects of EO, but this effect does not seem to be mediated via 5-HT(1A) or benzodiazepine receptors.

No abstract

No abstract

Cryptococcal infection had an increased incidence in last yearsCryptococcal infections have increased dramatically over the last years. This high incidence can be due in large part to the explosion of acquired immune deficiency syndrome (AIDS) epidemic around the world and the use of more potent immunosuppressive agents by increasing numbers of solid organ transplant recipients (Mitchell & Perfect 1995, Dromer et al. 1996.Cryptococcal meningitis, the most common infection of cryptococcosis is usually chronic and uniformly fatal if untreated (Collazos 2003). Some antifungal drugs, such as polyene macrolides (amphotericin B) and azoles (itraconazole and fluconazole) are currently used in antifungal therapies with certain limitations due to side effects as toxicity and emergence of resistant strains (Terrel 1999, Saag et al. 2000. The lack of response to treatment and resistance in vitro to fluconazole, the drug that now commands maintenance treatment protocols for AIDS patients has began to emerge with Cryptococcus neoformans var. neoformans in immunocompromissed patients undergoing prolonged azole treatment (Alves et al. 1997, Momoff & Parrish 2003 The medicinal plants have been used for several purposes including antimicrobial effects and have showed inhibition of growth to fungi. Caryocar brasiliensis, plant widely distributed in Brazil, has in vitro activity against Paracoccidioides brasiliensis and C. neoformans while Hyptis ovalifolia, plant native from Brazilian cerrado, has inhibitory effect on dermatophytes (Souza et al. 2002). We are interested on antifungal activity of Ocimum gratissimum, plant known as alfavaca cravo, which has presented in vitro inhibitory effect against bacteria as Staphylococcus aureus, Escherichia coli, and some fungi as dermatophytes (Lima et al. 1993, Nakamura et al. 1999.The occurrence of cryptococcosis in Goiânia and its importance in immunocom-promised patients justify in studying Cryptococcus species in this city localized in the Brazilian midwest region. In this paper the antifungal activity of ethanolic crude extract, ethyl acetate, hexane and chloroformic fractions, essential oils and eugenol from O. gratissimum leaves towards 25 isolates of C. neoformans, important pathogen commonly found in our geographic area , was investigated. Chemical analysis of essential oil -Oil sample analysis was performed on a Shimadzu QP5050A gas chromatograph interfaced to a mass spectrometer (GC/MS) instrument employing the following conditions: fused silica capillary column (CBP-5; 30 m x 0.25 µm x 0.25 µm) which was programmed as follows: 60ºC for 2 min and then up to 240ºC at 3ºC/min, then to 270ºC at 10ºC/min ending with a 10 min at 270ºC. The carrier gas was He at a flow rate of 1 ml/min, split mode, with ratio of 1:5, and injection volume of 1 µl in CH 2 Cl 2 and the ionization voltage, 70 EV. The calculation of the retention indexes was made through co-injection with C 8 -C 32 n alkanes series (Van Den Doll & Kratz 1963). Identification of the oil constituents was made based on the ...

No abstract

Preparations from Pimenta pseudocaryophyllus (Gomes) L.R. Landrum (Myrtaceae) have been widely used in Brazilian folk medicine. This study aims to evaluate the antimicrobial activity of the crude ethanol extracts, fractions, semipurified substances, and essential oils obtained from leaves of two chemotypes of P. pseudocaryophyllus and to perform the antinociceptive and anti-inflammatory screening. The ethanol extracts were purified by column chromatography and main compounds were spectrally characterised (1D and 2D 1H and 13C NMR). The essential oils constituents were identified by GC/MS. The broth microdilution method was used for testing the antimicrobial activity. The abdominal contortions induced by acetic acid and the ear oedema induced by croton oil were used for screening of antinociceptive and anti-inflammatory activities, respectively. The phytochemical analysis resulted in the isolation of pentacyclic triterpenes, flavonoids, and phenol acids. The oleanolic acid showed the best profile of antibacterial activity for Gram-positive bacteria (31.2–125 μg mL−1), followed by the essential oil of the citral chemotype (62.5–250 μg mL−1). Among the semipurified substances, Ppm5, which contained gallic acid, was the most active for Candida spp. (31.2 μg mL−1) and Cryptococcus spp. (3.9–15.6 μg mL−1). The crude ethanol extract and fractions from citral chemotype showed antinociceptive and anti-inflammatory effects.

In the context of developing a new natural product-based cosmetic, the in vitro efficacy and safety evaluations of a complex botanical mixture based on Eugenia dysenterica leaf hydroalcoholic extract (EDE) (2.5-1000μg/mL) were carried out. Chromatographic analysis demonstrated the presence of the tannin (ellagic acid) and flavonoids (quercetin and gallic acid) which characterize the EDE as a polyphenol-rich mixture. Using HFF-1 fibroblasts, it was shown that EDE promoted cell regeneration after UVA exposure. It also led to the inhibition of the collagenase, elastase and tyrosinase enzymes, which are involved in skin-related disorders. In terms of toxicological evaluation, the EDE was classified as non-phototoxic through the 3T3 Neutral Red Uptake Phototoxicity Test (OECD N° 432, 2004) and non-eye irritant by Bovine Corneal Opacity and Permeability (OECD N° 437, 2013) assay, in conjunction with corneal histomorphometric analysis. Furthermore, the EDE has no skin sensitization potential as demonstrated by a two-out-of-three prediction model [protein-binding/haptenization (OECD N° 442C, 2015), keratinocyte and dendritic cell activations]. In addition, it was shown that the EDE seems to be non-genotoxic through the cytokinesis-block micronucleus assay (OECD N° 487, 2014) using HepG2 cells. When considered together, these findings support the use of EDE botanical mixture in cosmetic/pharmaceutical products.

No abstract