Evaluation of the antioedematogenic, free radical scavenging and antimicrobial activities of aerial parts of Tillandsiastreptocarpa Baker-Bromeliaceae.

The crude methanolic extract of the aerial parts of Tillandsiastreptocarpa was investigated for their acute toxicity and antioedematogenic, antioxidant and antimicrobial activities. Also, the antioedematogenic activity of the hexane fraction resulting from the partition of the crude methanolic extract was evaluated. The methanolic extract and the hexane fraction showed significant (P < 0.05) inhibition of ear oedema, observed at 2 mg/ear in the croton oil-induced mice ear oedema test. In the 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging test, a high reactivity and potent antioxidant effect (IC(50) = 0.0056%, w/v) were observed for the methanolic extract. The antimicrobial activity assay showed that the crude methanolic extract was inactive toward Escherichiacoli, Staphylococcusaureus, Pseudomonasaeruginosa, Bacillussubtilis, Candidaalbicans, C. parapsilosis, C. krusei and C. tropicalis (MIC > 500 microg/ml). The methanolic extract showed no toxic effect on mice at a single dose of 2000 mg/kg (p.o). Common side effects including mild diarrhoea, loss of weight and depression were not recorded. The compounds cycloartenol, 4',5-dihydroxy-3',7-dimethoxyflavanone and a mixture of the steroids stigmasterol, beta-sitosterol and campesterol, were isolated from the hexane fraction and identified by spectroscopic methods.

Protective effects of Mangifera indica L. extract, mangiferin and selected antioxidants against TPA-induced biomolecules oxidation and peritoneal macrophage activation in mice.

We compared the protective abilities of Mangifera indica L. stem bark extract (Vimang) 50-250 mgkg(-1), mangiferin 50 mgkg(-1), vitamin C 100 mgkg(-1), vitamin E 100 mgkg(-1)and beta -carotene 50 mgkg(-1)against the 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced oxidative damage in serum, liver, brain as well as in the hyper-production of reactive oxygen species (ROS) by peritoneal macrophages. The treatment of mice with Vimang, vitamin E and mangiferin reduced the TPA-induced production of ROS by the peritoneal macrophages by 70, 17 and 44%, respectively. Similarly, the H(2)O(2)levels were reduced by 55-73, 37 and 40%, respectively, when compared to the control group. The TPA-induced sulfhydryl group loss in liver homogenates was attenuated by all the tested antioxidants. Vimang, mangiferin, vitamin C plus E and beta -carotene decreased TPA-induced DNA fragmentation by 46-52, 35, 42 and 17%, respectively, in hepatic tissues, and by 29-34, 22, 41 and 17%, in brain tissues. Similar results were observed in respect to lipid peroxidation in serum, in hepatic mitochondria and microsomes, and in brain homogenate supernatants. Vimang exhibited a dose-dependent inhibition of TPA-induced biomolecule oxidation and of H(2)O(2)production by peritoneal macrophages. Even if Vimang, as well as other antioxidants, provided significant protection against TPA-induced oxidative damage, the former lead to better protection when compared with the other antioxidants at the used doses. Furthermore, the results indicated that Vimang is bioavailable for some vital target organs, including liver and brain tissues, peritoneal exudate cells and serum. Therefore, we conclude that Vimang could be useful to prevent the production of ROS and the oxidative tissue damages in vivo.

Differences in heart rate variability between cardioinhibitory and vasodepressor responses to head-up tilt table testing.

BACKGROUND: Patients with syncope show different responses to head-up tilt (HUT) test, which may be due to different pathophysiological mechanisms. METHODS: HUT (70 degrees) was performed in 24 patients who experienced recurrent syncope. Nine patients had a cardioinhibitory (CI) response, 7 patients had a vasodepressor (VD) response, and 8 patients had a mixed (MX) response. Heart rate variability was analyzed at 60-sec periods during HUT. RESULTS: Total spectrum (TS) was greater at rest and 1 min after syncope in the CI and MX groups as compared to the VD group. Low frequency spectrum (LF) was significantly greater during rest and the first minute after syncope in the CI groups as compared with the VD group. After the rest period, the CI and MX groups showed more elevated high frequency spectrum (HF) values than the VD group (p < 0.01). One minute after syncope, the HF increased in the CI and MX groups but not in the VD group (p < 0.01). The VD group showed higher LF/HF ratio from the beginning of rest (3.9 +/- 4.1) as compared to the CI and MX groups (p < 0.01). This difference was most significant 2 min before syncope occurred. The CI and MX groups showed greater pNN50 and rMSSD as compared to the VD group. CONCLUSIONS: Our results suggest that vagal tone is higher in subjects showing cardioinhibitory and mixed responses to HUT. In contrast, patients with a vasodepressor response showed predominantly sympathetic activity. These findings suggest that there are different pathophysiological mechanisms underlying syncope.