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1.
Hist Sci Med ; 40(2): 115-28, 2006.
Article in French | MEDLINE | ID: mdl-17152523

ABSTRACT

Count Henri de Bonneval, was born in Bordeaux in 1806, in the line of descent of one of the most ancient French families of noble rank. He was assistant manager of the Strasbourg stud farm in 1830, when Louis-Philippe, an Orleanist, ascended to the throne of the Bourbon Charles X. As several other legitimists, Count Henri refused to take an oath to the new king and prefered to resign his position. Interested in medicine, he was deeply impressed by Hahnemann's Organon der Heilkunst and decided to leave France for KOthen, in Saxony, in order to learn homeopathy directly from its founder Back to France, he defended in Montpellier the first French medical thesis devoted to homeopathy and then opened a consulting room in Bordeaux. He rapidly gained a solid reputation and a large audience as a practitioner of homeopathy. At the same time, Henri acquired the Chateau de Latresne and the 500 acres surrounding land. He renovated and brought up to date the agricultural and wine-producing activities of the estate. The medical doctor soon proved to be an expert agronomist, extending his competence to the famous vineyard Chateau Canon of St. Emilion. Throughout his life, the Count showed notable qualities of philanthropy, materialized at Latresne by the construction of a church and, adjacent to the chapel, a boarding school, two classrooms and shelters for poor or sick old people. At the end of his life, Henri de Bonneval wrote a comprehensive book, that includes the presentation and discussions of the homeopathic methods, some philosophical reflections and personal memories.


Subject(s)
Agriculture/history , Homeopathy/history , Charities/history , France , History, 19th Century , Wine/history
2.
J Steroid Biochem Mol Biol ; 82(2-3): 233-9, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12477490

ABSTRACT

In different cell systems, the lipido-sterolic extract of Serenoa repens (LSESr, Permixon inhibits both type 1 and type 2 5alpha-reductase activity (5alphaR1 and 5alphaR2). LSESr is mainly constituted of fatty acids (90+/-5%) essentially as free fatty acids (80%). Among these free fatty acids, the main components are oleic and lauric acids which represent 65% and linoleic and myristic acids 15%. To evaluate the inhibitory effect of the different components of LSESr on 5alphaR1 or 5alphaR2 activity, the corresponding type 1 and type 2 human genes have been cloned and expressed in the baculovirus-directed insect cell expression system Sf9. The cells were incubated at pH 5.5 (5alphaR2) and pH 7.4 (5alphaR1) with 1 or 3nM testosterone in presence or absence of various concentrations of LSESr or of its different components. Dihydrotestosterone formation was measured with an automatic system combining HPLC and an on-line radiodetector. The inhibition of 5alphaR1 and 5alphaR2 activity was only observed with free fatty acids: esterified fatty acids, alcohols as well as sterols assayed were inactive. A specificity of the fatty acids in 5alphaR1 or 5alphaR2 inhibition has been found. Long unsaturated chains (oleic and linolenic) were active (IC(50)=4+/-2 and 13+/-3 microg/ml, respectively) on 5alphaR1 but to a much lesser extent (IC(50)>100 and 35+/-21 microg/ml, respectively) on 5alphaR2. Palmitic and stearic acids were inactive on the two isoforms. Lauric acid was active on 5alphaR1 (IC(50)=17+/-3 microg/ml) and 5alphaR2 (IC(50)=19+/-9 microg/ml). The inhibitory activity of myristic acid was evaluated on 5alphaR2 only and found active on this isoform (IC(50)=4+/-2 microg/ml). The dual inhibitory activity of LSESr on 5alpha-reductase type 1 and type 2 can be attributed to its high content in free fatty acids.


Subject(s)
Androgen Antagonists/pharmacology , Fatty Acids, Nonesterified/pharmacology , Oxidoreductases/antagonists & inhibitors , Plant Extracts/pharmacology , Animals , Cell Line , Cholestenone 5 alpha-Reductase , Fatty Alcohols/pharmacology , Humans , Hypolipidemic Agents/pharmacology , Isoenzymes/antagonists & inhibitors , Isoenzymes/metabolism , Oxidoreductases/metabolism , Serenoa , Sitosterols/pharmacology , Tocopherols/pharmacology
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