Acute Hypotensive, Diuretic and Antioxidant Activities Induced by Urtica circularis

Aims: The aim of this study was to investigate the possible hypotensive and diuretic effects of ethanolic extract of Urtica circularis (Hicken) Sorarú (Urticaceae) using preclinical methods. Place and Duration of Study: Department of Pharmacology, School of Pharmacy and Biochemistry, Universidad de Buenos Aires, from July 2015 to January 2016. Methodology: Effect on blood pressure and heart rate on anaesthetized normotensive and hypertensive rats were measured using Statham Gould P23ID pressure transducer coupled to a Grass 79D polygraph. Rats were placed in metabolic cages in order to collect urine. Urinary volume was measured and sodium and potassium concentration was estimated from each urine sample using indirect ion-selective electrode potentiometry. The vasorelaxant activity of major compound was studied using isolated aortic rings. Antioxidant activity was estimated measuring 2,2 diphenyl 2 picryl hydrazyl hydrate radical scavenging activity. Results: The intravenous administration of the extract of U. circularis (0.1–30 mg/kg) in anaesthetized normotensive and hypertensive rats caused a dose-dependent reduction in the mean arterial pressure without affecting the heart rate. The greater reduction of blood pressure induced by U. circularis was observed in hypertensive rats (30 mg/kg: Spontaneously Hypertensive Rat: -34.7±3.3 mmHg, Spague Dawley: -18.3±3.9 mmHg). Cumulative urinary excretions 24 h after treatment with the extract 100 and 300 mg/kg were 18.2±1.2 and 14.9±1.5 mL respectively, significantly higher than the control group (9.0±1.3 mL). The addition of cumulative concentrations of vicenin-2 (10-7-10-4M) generated relaxation in endothelium-intact aortic rings pre-contracted with 10–7M Phenylephrine (Emax = 66.2±3.5%). Extract showed antioxidant activity reaching 45% of DPPH scavenging activity at 1000 μg/mL, meanwhile the flavonoid reached 20% of scavenger capacity. Conclusion: U. circularis, has a diuretic, antioxidant and hypotensive effect. Vicenin-2, the major component of this extract showed vasorelaxant activity, potentially responsible for the properties of the extract.Fil: Rodriguez Basso, A.. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Farmacología; ArgentinaFil: Marrassini, Carla. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Anesini, Claudia Alejandra. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Gorzalczany, Susana Beatriz. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Farmacología; Argentin

Refashioning the Ethiopian monarchy in the twentieth century: An intellectual history

This article traces the shift in the Ethiopian monarchical ideology from lineage as symbolic Christian filiation to dynasty as a political genealogy of sovereign power. From the end of the nineteenth century, and more prominently under Haylä Səllase, Ethiopian state sources started qualifying the Ethiopian ruling dynasty as ‘unbroken’ in history. A record of ‘uninterrupted’ power allowed the Ethiopian government to politically appropriate past glories and claim them as ‘ours’, thus compensating for the political weakness of the present with the political greatness of the past. The ideological rebranding of the Ethiopian monarchy in the 1930s brought Ethiopia closer to Japan, and the ‘eternalist clause’ of the Meiji constitution offered a powerful model of how to recodify dynasty in modern legal terms. An intellectual history of dynasty in the Ethiopian context sees the concept simultaneously associated with both hegemonic and counter-hegemonic political projects. The narratives of continuity enabled by the dynastisation of history were successful in invigorating the pro-Ethiopian front during the Italian occupation of Ethiopia (1936-1941), but served at the same time to reinforce domestic mechanisms of class, political and cultural domination

Organic solvent-luteolin interactions studied by FT-Raman, Vis-Raman, UV-Raman spectroscopy and DFT calculations

The interactions of luteolin with three alcohols (methanol, 1-propanol, 1-butanol) and dimethylsulfoxide (DMSO) were studied by FT-Raman, Vis-Raman and UV-Raman spectroscopies, coupled to density functional theory calculations. No large shift was observed for the bands in the spectra of luteolin in alcohols or DMSO in the 1700-1550 cm-1 region. This is possibly related to the presence of a strong intramolecular hydrogen bond involving the 5-OH and the carbonyl of luteolin, as suggested by literature data [V. Exarchou, A. Troganis, I.P. Gerothanassis, M. Tsimidou, D. Boskou, Tetrahedron 2002, 58, 7423-7429] and DFT calculations. Furthermore, DFT calculations suggest that the CO stretching of luteolin is implicated in several vibrational modes, whereas the most upshifted band in the 1700-1550 cm-1 can be interpreted as arising mainly from a 5-OH bending. The results are discussed in the framework of vibrational spectroscopy studies on flavonoids, of the photophysical properties of luteolin, and of the reported literature of vibrational spectra of luteolin under different conditions, in particular when interacting with biomolecules

Antiproliferative activity of aqueous and polyphenol-rich extracts of Larrea divaricata Cav. upon a melanoma cell line

Abstract: Most of the deaths from skin cancer are caused by melanoma, a malignancy in which STAT3 plays a crucial role. The inhibition of STAT3 is considered a potential target to induce cell death, tumor regression and metastasis inhibition. The objective of this work was to evaluate the activity of the aqueous extract of Larrea divaricata (Aq), a fraction rich in polyphenols (EA),and the isolated compound quercetin-3-methyl ether (Q3ME) on B16F10 melanoma cells. The effects of Aq, EA and Q3ME were assessed on B16F10 cells by determining the proliferation, viability, apoptosis induction and the expression and phosphorylation of STAT3. The phytochemical composition of the extracts was determined by High Performance Liquid Chromatography. Aq, EA and Q3ME presented antiproliferative activity on B6F10 cells through p-STAT3 inhibition and early and late apoptosis induction (EC50 EA= ≤0.1 μg/ml; Aq= 316±30 μg/ml; Q3ME= <0.1 μg/ml). L. divaricata could be considered for the development of adjuvant phytotherapies in melanoma treatment