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Featured researches published by Alassane Wélé.


Nutrition & Metabolism | 2009

In vitro vasorelaxation mechanisms of bioactive compounds extracted from Hibiscus sabdariffa on rat thoracic aorta

Mamadou Sarr; Saliou Ngom; Modou Oumy Kane; Alassane Wélé; Doudou Diop; Bocar Sarr; Lamine Gueye; Ramaroson Andriantsitohaina; Aminata Sall Diallo

BackgroundIn this study, we suggested characterizing the vasodilator effects and the phytochemical characteristics of a plant with food usage also used in traditional treatment of arterial high blood pressure in Senegal.MethodsVascular effects of crude extract of dried and powdered calyces of Hibiscus sabdariffa were evaluated on isolated thoracic aorta of male Wistar rats on organ chambers. The crude extract was also enriched by liquid-liquid extraction. The various cyclohexane, dichloromethane, ethyl acetate, butanol extracts obtained as well as the residual marc were subjected to Sephadex LH-20 column chromatography. The different methanolic eluate fractions were then analyzed by Thin Layer (TLC) and High Performance Liquid Chromatography (HPLC) and their vascular effects also evaluated.ResultsThe H. Sabdariffa crude extract induced mainly endothelium-dependent relaxant effects. The endothelium-dependent relaxations result from NOS activation and those who not dependent to endothelium from activation of smooth muscle potassium channels. The phytochemical analysis revealed the presence of phenolic acids in the ethyl acetate extract and anthocyans in the butanolic extract. The biological efficiency of the various studied extracts, in term of vasorelaxant capacity, showed that: Butanol extract > Crude extract > Residual marc > Ethyl acetate extract. These results suggest that the strong activity of the butanolic extract is essentially due to the presence of anthocyans found in its fractions 43-67.ConclusionThese results demonstrate the vasodilator potential of hibiscus sabdariffa and contribute to his valuation as therapeutic alternative.


Chemistry & Biodiversity | 2017

Chemical Diversity and Antimicrobial Activity of Volatile Compounds from Zanthoxylum zanthoxyloides Lam. according to Compound Classes, Plant Organs and Senegalese Sample Locations

Yoro Tine; Abdoulaye Diop; William Diatta; Jean-Marie Desjobert; Cheikh Saad Bouh Boye; Jean Costa; Alassane Wélé; Julien Paolini

The chemical diversity of Zanthoxylum zanthoxyloides growing wild in Senegal was studied according to volatile compound classes, plant organs and sample locations. The composition of fruit essential oil was investigated using an original targeted approach based on the combination of gas chromatography (GC) and liquid chromatography (LC) both coupled with mass spectrometry (MS). The volatile composition of Z. zanthoxyloides fruits exhibited relative high amounts of hydrocarbon monoterpenes (24.3 – 55.8%) and non‐terpenic oxygenated compounds (34.5 – 63.1%). The main components were (E)‐β‐ocimene (12.1 – 39%), octyl acetate (11.6 – 21.8%) and decanol (9.7 – 15.4%). The GC and GC/MS profiling of fruit essential oils showed a chemical variability according to geographical locations of plant material. The LC/MS/MS analysis of fruit oils allowed the detection of seven coumarins in trace content. The chemical composition of fruit essential oils was compared with volatile fractions of leaves and barks (root and trunk) from the same plant station. Hexadecanoic acid, germacrene D and decanal were identified as the major constituents of leaves whereas the barks (root and trunk) were dominated by pellitorine (85.8% and 57%, respectively), an atypic linear compound with amide group. The fruit essential oil exhibited interesting antimicrobial activities against Staphylococcus aureus and Candida albicans, particularly the alcohol fraction of the oil.


Molecules | 2017

A Method for LC-MS/MS Profiling of Coumarins in Zanthoxylum zanthoxyloides (Lam.) B. Zepernich and Timler Extracts and Essential Oils

Yoro Tine; Franck Renucci; Jean Costa; Alassane Wélé; Julien Paolini

The metabolites from the coumarin class, present in tissues of plants belonging mainly to the Rutaceae and Apiaceae families, included compounds with high chemical diversity such as simple coumarins and furocoumarins. These health-promoting components are recognized for their valuable biological activities in herbal preparations but also for their phototoxic effects. In this work, a targeted liquid chromatography (LC) coupled with tandem mass spectrometry (MS2) was developed for the screening of 39 reference standards of coumarins and furocoumarins in essential oils and plant extracts. Chromatographic separation was accomplished on reversed phase column using water/acetonitrile as the mobile phase and detection was performed on a hybrid QqQ/linear ion trap spectrometer fitted with an atmospheric pressure chemical ionization (APCI) source operating in positive ion mode. This analytical approach was applied to investigate the coumarin compositions of fruit essential oils and methanolic extracts obtained from separated parts (fruit, leaf, stem, trunk, and root) of Zanthoxylum zanthoxyloides. Ten coumarins and six furanocoumarins were reported in this species and data analyses were used to assess the suitability of these compounds to the metabolomics-based differentiation of plant organs. The quantification criteria of the metabolites in extract samples included linearity, limit of quantification, limit of detection, and matrix effect were validated. As reported for other species of the Rutaceae family, the concentration of coumarins was drastically higher in Z. zanthoxyloides fruits than in other plant organs.


Nigerian Journal of Natural Products and Medicine | 2006

Isolation and characterization of three cyclopeptides from the seeds of Annona glauca and A. cherimola

Alassane Wélé; Yanjun Zhang; Lionel Dubost; Jean-Louis Pousset; Bernard Bodo

This paper describes the isolation and structure elucidation of three cytotoxic cyclopeptides, named glaucacyclopeptide B (2), cherimolacyclopeptide G (1) and H (2), from the seeds of Annona glauca and A. cherimola . Techniques used in the structure determination included MS/MS fragmentation using a QTOF mass spectrometer equipped with an ESI source, chemical degradation and one- and two dimensional NMR and IR spectroscopy. Keywords : annonaceae, seeds, cyclopeptides, glaucacyclopeptide B; cherimolacyclopeptide G, cherimolacyclopeptide H Nigerian Journal of Natural Products and Medicine Vol. 9 2005: 68-72


Journal of Natural Products | 2004

A cytotoxic cyclic heptapeptide from the seeds of Annona cherimola.

Alassane Wélé; Yanjun Zhang; Idrissa Ndoye; Jean-Paul Brouard; Jean-Louis Pousset; Bernard Bodo


Phytochemistry | 2005

Two cyclopeptides from the seeds of Annona cherimola

Alassane Wélé; Yanjun Zhang; Jean-Paul Brouard; Jean-Louis Pousset; Bernard Bodo


Phytochemistry | 2005

Cherimolacyclopeptide D, a novel cycloheptapeptide from the seeds of Annona cherimola.

Alassane Wélé; Idrissa Ndoye; Yanjun Zhang; Jean-Paul Brouard; Bernard Bodo


Tetrahedron | 2009

3D-structure of cycloreticulin C and glabrin A, cyclopeptides from the seeds of Annona reticulata

Alassane Wélé; Claudine Mayer; Dermigny Quentin; Yanjun Zhang; Alain Blond; Bernard Bodo


Chemical & Pharmaceutical Bulletin | 2006

Cyclic Peptides from the Seeds of Annona glauca and A. cherimola

Alassane Wélé; Yanjun Zhang; Lionel Dubost; Jean-Louis Pousset; Bernard Bodo


Phytochemistry | 2005

Glaucacyclopeptide A from the seeds of Annona glauca

Alassane Wélé; Idrissa Ndoye; Yanjun Zhang; Jean-Paul Brouard; Jean-Louis Pousset; Bernard Bodo

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Bernard Bodo

Centre national de la recherche scientifique

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Yanjun Zhang

Centre national de la recherche scientifique

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Jean-Paul Brouard

Centre national de la recherche scientifique

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Idrissa Ndoye

Cheikh Anta Diop University

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Yoro Tine

Cheikh Anta Diop University

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Lamine Gueye

Cheikh Anta Diop University

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Mamadou Sarr

Cheikh Anta Diop University

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Christelle Caux

Centre national de la recherche scientifique

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