Françoise Bévalot

Vasorelaxant and hypotensive effects of a hydroalcoholic extract from the fruits of Nitraria sibirica Pall. (Nitrariaceae).

ETHNOPHARMACOLOGICAL RELEVANCE Fruits of Nitraria sibirica Pall. are traditionally used in Uighur medicine to treat hypertension. This study aimed to support that folk use by defining their vasoactive and hypotensive properties. MATERIALS AND METHODS The vasorelaxant activity and the underlying mechanisms of a hydroalcoholic extract from the fruits of Nitraria sibirica Pall. (NSHE) were evaluated on thoracic aortic rings isolated from Wistar rats. In addition, the acute hypotensive effect of NSHE was assessed in anesthetized spontaneously hypertensive rats (SHR) and in their normotensive control Wistar Kyoto (WKY) rats. RESULTS NSHE (0.1-10 g/l) was clearly more effective to induce vasodilation of phenylephrine- (PE, 1 μM) than high KCl- (60mM) pre-contracted aortic rings with respective E(max) values of 82.9±2.2% and 34.8±3.6%. The removal of endothelium almost abolished the relaxant effect of the extract. In addition, pre-treatment with N(w)-nitro-L-arginine-methyl ester (L-NAME, 100 μM), atropine (1 μM) or charybdotoxin (30 nM) plus apamin (30 nM), respective blockers of nitric oxide (NO) synthase, muscarinic receptors and endothelium-derived hyperpolarizing factor (EDHF), significantly reduced the observed effect of NSHE. By contrast, the cyclooxygenase (COX) inhibitor indomethacin (10 μM) or the K(+) channels blockers glibenclamide (10 μM), iberiotoxin (30 nM) and 4-amino-pyridine (4-AP, 1 mM) failed to modify the vasodilation. Finally, the acute intravenous injection of NSHE (1, 5, 10, 20 mg/kg) induced an immediate and transient hypotensive effect in anesthetized SHR and in WKY rats. CONCLUSIONS This experimental animal study suggests that hydroalcoholic extract from the fruits of Nitraria sibirica Pall. induces vasorelaxation through an endothelium-dependent pathway involving NO synthase (NOS) activation, EDHF production and muscarinic receptor stimulation. Additionally, our results determine that this vasorelaxant effect is translated by a significant hypotensive effect.

Mechanisms of vasorelaxation induced by Ziziphora clinopodioides Lam. (Lamiaceae) extract in rat thoracic aorta

AIM OF THE STUDY Ziziphora clinopodioides Lam. (ZC) is widely used in Uyghur folk medicine for the treatment of hypertension diseases in Xinjiang, an autonomous region of China. To provide pharmacological basis for this traditional use, we explored the vasodilating effects of ZC and investigated the underlying mechanisms. MATERIALS AND METHODS Activity of hexane (ZCHE), dichloromethane (ZCDE) and aqueous (ZCAE) extracts of ZC were evaluated on isolated rat aortic rings pre-contracted with phenylephrine (PE) or high KCl. The mechanisms were evaluated on ZCDE, the most potent extract. RESULTS ZCDE-induced relaxation in endothelium-intact aortic rings pre-contracted with phenylephrine (PE, 10(-6) M) or high KCl (6×10(-2) M), with respective EC(50) values of 0.27±0.03 and 0.34±0.04 g/l. Mechanic removal of the endothelium did not significantly modify ZCDE-induced relaxation. In endothelium-denuded aorta pre-contracted with PE (10(-6) M), the vasorelaxant effect of ZCDE was significantly decreased by 4-amino-pyridine (10(-3) M), but not by glibenclamide (10(-4) M), iberiotoxin (3×10(-8) M) and thapsigargin (10(-7) M). In Ca(2+) free solution, ZCDE significantly inhibited extracellular Ca(2+)-induced contraction in high KCl and PE pre-contracted rings. Additionally ZDCE inhibited the intracellular Ca(2+) release sensitive to PE (10(-6) M). CONCLUSIONS The results demonstrate that ZDCE exhibits endothelium-independent vasodilating properties that are mediated by inhibition of extracellular Ca(2+) influx through voltage- and receptor-operated Ca(2+) channels (VDDCs and ROCCs), by inhibition of Ca(2+) release from intracellular stores, and also by the opening of voltage-dependent K(+) channels.

Acetophenones and other constituents from the roots of Melicope erromangensis

Octandrenolone and five novel related dimethylpyran acetophenones have been isolated from the chloroform extract of roots of Melicope erromangensis and identified by spectroscopic studies and chemical correlations as O-methyloctandrenolone, (+)-trans-3‴,4‴-dihydro-3‴,4‴-dihydroxy-O-methyloctandrenolone, (+)-trans- 3″,4″-dihydro-3″,4″-dihydroxy-O-methyloctandrenolone, and trans-3″,4″-dihydro-3″,4″-dihydroxyoctandrenolone. In addition, four known quinolines and three known flavones have been isolated.

New insights into the mechanisms of the vasorelaxant effects of apocynin in rat thoracic aorta.

Apocynin is a naturally occurring acetophenone widely used as an inhibitor of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase. Recent data suggested that apocynin might exert NADPH oxidase‐independent pharmacological properties. Among them, vasorelaxant properties have been described, but the mechanisms still give rise to debates. The present study investigated the mechanisms involved in the vasorelaxant effect of apocynin on the in vitro model of rat isolated thoracic aortic rings. Apocynin (30 μm to 10 mm) induced a dose‐dependent relaxation in both endothelium‐intact and endothelium‐denuded aortic rings with respective EC50 values of 0.78 ± 0.08 and 1.91 ± 0.21 mm. Endothelium removal or inhibition of nitric oxide (NO) synthase with Nω‐nitro‐l‐arginine‐methyl ester (l‐NAME) significantly decreased but did not abolish the effect of apocynin. By contrast, apocynin‐induced relaxation was unchanged after incubation with indomethacin or charybdotoxin plus apamin. In endothelium‐denuded aortas, the vasorelaxant effect of apocynin was significantly reduced by glibenclamide but not by 4‐aminopyridine nor by iberiotoxin. Apocynin significantly decreased Ca2+‐induced contraction and inhibited intracellular Ca2+mobilization after contraction with phenylephrine. Finally, the acute intravenous injection of apocynin led to an immediate and transient hypotensive effect in spontaneously hypertensive rats (SHR). In conclusion, our data demonstrated that apocynin induces both endothelium‐independent relaxant effects involving inhibition of Ca2+mobilization and activation of KATP channels in vascular smooth muscle cells and endothelium‐dependent effects mediated by NO. These results should provide a basis for caution when interpreting results on the vascular effects of apocynin.

Bioassay-guided isolation of vasorelaxant compounds from Ziziphora clinopodioides Lam. (Lamiaceae)

Ziziphora clinopodioides Lam. (Lamiaceae) is traditionally used in Uighurs medicine for the treatment of hypertension. Our study determined and evaluated the bioactive compounds by performing an activity-guided fractionation of a hydroalcoholic extract of the whole plant, using an in vitro model of rat isolated thoracic aortic rings. Seven compounds were identified as active principles: acacetin, apigenin, chrysin, thymonin, acetovanillone, 4-hydroxyacetophenone and ethyl 4-coumarate. Apigenin, chrysin and ethyl 4-coumarate were found to be the most effective. Our results provide the first evidence that the vasodilation induced by Z. clinopodioides Lam. is mediated, at least in part, by phenolic components.

Coumarins from Three Phebalium species

The twigs of Phebalium anceps yielded the common furocoumarins psoralen, bergapten and xanthotoxin whereas the leaves of P. coxii and P. ralstonii gare only 8-prenylated 7-methoxycoumarins. From R coxii murrangatin and murralongin were obtained whilst R ralstonii yielded both of these compounds and another coumarin, the novel 7-methoxy-8-(2-acetoxy-3-methyl-1oxobut-2-enyl)-coumarin. The chemotaxonomic implications of these results are discussed.

Alkaloids from stem bark of dutaillyea baudouinii

Abstract The stem bark of Dutaillyea baudouinii yielded five quinolines. Two were the known furoquinolines, evoxine and haplopine, two were new dihydrofuroqunolines, 7,8-dimethoxyplatydesmine and 7,8-dimethoxymyrtopsine, and one was a new dihydropyranoquinoline, 8,9-dimethoxygeibalansine.

Zanthomamide: An aromatic amide from Zanthoxylum thomense

Abstract From the stem bark of Zanthoxylum thomense a new amide, zanthomamide has been isolated and characterized as N -methyl, N -cinnamyl-(3′,4′-methylenedioxy)-phenylethylamine. Other constituents identified are the known benzophenanthridines, decarine, norchelerythrine and angoline.

Paracotoin derivatives from leaves of Ticorea pedicellata

Abstract Three new paracotoin derivatives have been isolated from the leaves of Ticorea pedicellata and identified as 4,5-dimethoxyparacotoin, 4,5,2′-trimethoxyparacotoin and 4,2′-dimethoxyparacotoin by full spectral analysis. The chemotaxonomic implications of the occurrence of paracotoin-type compounds in the Rutaceae are briefly discussed.

Phebaclavin I, a novel 3-prenylated coumarin, and trichoclin acetate, a new natural furocoumarin, from the aerial parts of Phebalium aff. tuberculosum (Rutaceae).

Phebaclavin I, a novel 3-prenylated coumarin, was isolated from the aerial parts of Phebalium aff. tuberculosum (Rutaceae) together with five known related compounds, Phebaclavin A, B, D, G, H. The structure of phebaclavin I was established by spectroscopic methods. Several other known coumarins were obtained, including trichoclin acetate, a furocoumarin isolated for the first time from a natural source, but previously described from acetylation of trichoclin.