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1.
Article in English | MEDLINE | ID: mdl-35031531

ABSTRACT

To assess the validity of Yaakov Stern's theory, which postulates that the first cognitive deficits of Alzheimer disease are delayed in patients with high cognitive reserve, compared to those with low cognitive reserve, but this is subsequently associated with faster cognitive decline when cerebral lesions have reached a certain degree of severity. A retrospective study of 318 patients with Alzheimer disease without associated cerebral disorders, was performed at the Memory Clinic of the University Hospital of Strasbourg. The patients were divided into five groups according to their degree of cognitive reserve, as assessed by their level of education (primary, middle school, intermediate, high school and higher education). Cognitive status was assessed by scores on the Mini Mental Status Examination (MMSE) at the first examination and during follow-up lasting four years or longer. Slopes of cognitive decline were computed and compared between groups using ß linear regression. Patients in the higher education group had higher MMSE scores than those in the other groups at the first consultation, but a statistically significant steeper slope during the follow-up. Our results are consistent with Stern's theoretical model, which assumes that high cognitive reserve is accompanied by compensation mechanisms which hinder the onset of clinical cognitive decline in patients with Alzheimer disease, but that is then associated with a faster decline at a later stage when the reserve is exhausted.

2.
Geriatr Psychol Neuropsychiatr Vieil ; 19(2): 229-235, 2021 Jun 01.
Article in French | MEDLINE | ID: mdl-34080985

ABSTRACT

To appraise the validity of the Yaakov Stern's theory, which postulates that the first cognitive deficits of Alzheimer's disease are delayed in patients with high cognitive reserve, compared to those with low cognitive reserve, but is subsequently associated with faster cognitive decline when cerebral lesions have reached some degree of severity. A retrospective study of 318 patients with Alzheimer's disease without associated cerebral disorders, was performed in the Memory Clinic of the University Hospital of Strasbourg. The patients were divided into 5 groups according to the degree of cognitive reserve assessed by the level of education (primary, middle school, intermediary, high school and higher education). Cognitive status was assessed by the scores on the Mini Mental Status at the first examination and during a 4-year or more follow-up. Slopes of cognitive decline were computed and compared between groups by ß linear regression. Patients in the higher education group had higher MMSE scores than those in the other groups at the first consultation, but a statistically significant steeper slope during the follow-up. Our results are congruent with the Stern's theoretical model, assuming that high cognitive reserve brings into play compensation mechanisms which hinder the onset of clinical cognitive decline in patients with Alzheimer's disease, but then is associated with a faster decline at a later stage when the reserve is exhausted.


Subject(s)
Alzheimer Disease , Cognition Disorders , Cognitive Dysfunction , Cognitive Reserve , Disease Progression , Humans , Neuropsychological Tests , Retrospective Studies
3.
Chem Biodivers ; 9(4): 714-26, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22492490

ABSTRACT

We report here a novel reductive coupling reaction of conjugated, non- or poorly enolizable aldehydes induced by H(2) S and operative in aqueous solutions under prebiotically relevant conditions. This reaction leads from retinal to ß-carotene, and from benzylic aldehydes to the corresponding diarylethylenes. This novel reaction also opens a new potentially prebiotic pathway leading from glyoxylic acid to various compounds that are involved in the reductive tricarboxylic acid cycle. This C--C bond forming reaction of prebiotic interest might have been operative, notably, in the sulfide-rich environments of hydrothermal vents, which have been postulated as possible sites for the first steps of organic chemical evolution.


Subject(s)
Aldehydes/chemistry , Carbon/chemistry , Citric Acid Cycle , Oxidation-Reduction , Sulfites/chemistry , Water/chemistry
4.
Astrobiology ; 10(10): 973-88, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21162677

ABSTRACT

Laboratory experiments carried out under plausible prebiotic conditions (under conditions that might have occurred at primitive deep-sea hydrothermal vents) in water and involving constituents that occur in the vicinity of submarine hydrothermal vents (e.g., CO, H(2)S, NiS) have disclosed an iterative Ni-catalyzed pathway of C-C bond formation. This pathway leads from CO to various organic molecules that comprise, notably, thiols, alkylmono- and disulfides, carboxylic acids, and related thioesters containing up to four carbon atoms. Furthermore, similar experiments with organic compounds containing various functionalities, such as thiols, carboxylic acids, thioesters, and alcohols, gave clues to the mechanisms of this novel synthetic process in which reduced metal species, in particular Ni(0), appear to be the key catalysts. Moreover, the formation of aldehydes (and ketones) as labile intermediates via a hydroformylation-related process proved to be at the core of the chain elongation process. Since this process can potentially lead to organic compounds with any chain length, it could have played a significant role in the prebiotic formation of lipidic amphiphilic molecules such as fatty acids, potential precursors of membrane constituents.


Subject(s)
Carbon/chemistry , Chemistry, Organic/methods , Carbon Monoxide/chemistry , Catalysis , Chromatography, Gas , Mass Spectrometry , Nickel/chemistry , Organic Chemicals/analysis , Organic Chemicals/chemical synthesis , Organic Chemicals/chemistry , X-Ray Diffraction
5.
Org Lett ; 12(7): 1504-7, 2010 Apr 02.
Article in English | MEDLINE | ID: mdl-20218690

ABSTRACT

Four oleanane-related aromatic triterpenoids isolated from an archeological piece of oak wood have been identified by NMR studies. Their structures give clue to a novel diagenetic transformation pathway of 2,3-oxygenated higher plant triterpenoids in the environment.


Subject(s)
Triterpenes/chemistry , Indicators and Reagents/chemistry , Molecular Structure , Stereoisomerism , Triterpenes/isolation & purification , Wood/chemistry
6.
Anal Chim Acta ; 648(1): 85-97, 2009 Aug 19.
Article in English | MEDLINE | ID: mdl-19616693

ABSTRACT

Plant resins, and particularly dammars from the Dipterocarpaceae family, were widely used in the past, notably as part of caulking material. The organic composition of resins, already complicated, is not always preserved over time and can be considerably affected by ageing. Hence, their occurrence in archaeological items leads to the necessity to identify them taxonomically with precision. Resinous organic materials collected near and/or on wrecks discovered in South China Sea, supposed to contain dammar resins because of their geographical excavation context, were investigated by gas chromatography-mass spectrometry (GC-MS), together with freshly collected dammars, to establish taxonomic and alteration parameters allowing to identify dammar even in very altered samples or in mixtures together with other organic materials. This study specially focuses on three samples collected within or close to the M1J wreck, a Portuguese wreck lost in the Straight of Malacca during the 16th century. Our analyses establish that all three are made of dammar, two of them in association with pitch and bitumen. In addition, biodegradation biomarkers were detected in all these three samples, indicating that they were submitted to microbial degradation processes during their ageing.


Subject(s)
Dipterocarpaceae/chemistry , Resins, Plant/chemistry , Triterpenes/analysis , Archaeology , Asian People , Dipterocarpaceae/classification , Dipterocarpaceae/genetics , Gas Chromatography-Mass Spectrometry , Humans , Plant Bark/chemistry , Triterpenes/chemistry
7.
Anal Biochem ; 380(2): 202-10, 2008 Sep 15.
Article in English | MEDLINE | ID: mdl-18565321

ABSTRACT

The applicability of gas chromatography-combustion-isotope ratio mass spectrometry (GC-C-IRMS) for the quantification of 13C enrichment of proteinogenic amino acids in metabolic tracer experiments was evaluated. Measurement of the 13C enrichment of proteinogenic amino acids from cell hydrolyzates of Corynebacterium glutamicum growing on different mixtures containing between 0.5 and 10% [1-13C]glucose shows the significance of kinetic isotope effects in metabolic flux studies at low degree of labeling. We developed a method to calculate the 13C enrichment. The approach to correct for these effects in metabolic flux studies using delta13C measurement by GC-C-IRMS uses two parallel experiments applying substrate with natural abundance and 13C-enriched tracer substrate, respectively. The fractional enrichment obtained in natural substrate is subtracted from that of the enriched one. Tracer studies with C. glutamicum resulted in a statistically identical relative fractional enrichment of 13C in proteinogenic amino acids over the whole range of applied concentrations of [1-13C]glucose. The current findings indicate a great potential of GC-C-IRMS for labeling quantification in 13C metabolic flux analysis with low labeling degree of tracer substrate directly in larger scale bioreactors.


Subject(s)
Amino Acids/analysis , Carbon Isotopes/analysis , Corynebacterium glutamicum/metabolism , Gas Chromatography-Mass Spectrometry/methods , Isotope Labeling/methods , Amino Acids/metabolism , Carbon Isotopes/metabolism , Corynebacterium glutamicum/chemistry , Corynebacterium glutamicum/growth & development , Glucose/analysis , Glucose/metabolism , Glucose/pharmacokinetics , Kinetics
8.
Org Lett ; 7(14): 3041-4, 2005 Jul 07.
Article in English | MEDLINE | ID: mdl-15987200

ABSTRACT

[reaction: see text] The polyaromatic hydrocarbon 4,4'-dimethyldinaphtho[a,d]cycloheptane (1a) has been identified by NMR studies after isolation from an Oligocene sediment. The original symmetrical structure of 1a, which bears a central seven-membered ring, is closely related to higher plant triterpenoid precursor(s) of the serratane series and is believed to have been formed in the subsurface by a microbially mediated aromatization process.


Subject(s)
Triterpenes/chemistry , Triterpenes/isolation & purification , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular
9.
J Nat Prod ; 68(5): 759-61, 2005 May.
Article in English | MEDLINE | ID: mdl-15921424

ABSTRACT

Two new cyclic peroxides, 2 and 3, were isolated from a sample of the Norwegian sponge Plakortis simplex. Their structures including relative stereochemistry were elucidated by interpretation of MS and NMR data. Compound 3 exhibited moderate in vitro activity against six solid human tumor cell lines with IC50 values in the range 7-15 microg/mL.


Subject(s)
Antineoplastic Agents/isolation & purification , Peroxides/isolation & purification , Porifera/chemistry , Animals , Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Cyclization , Drug Screening Assays, Antitumor , Humans , Inhibitory Concentration 50 , Molecular Structure , Norway , Peroxides/chemistry , Peroxides/pharmacology , Tumor Cells, Cultured
11.
Org Lett ; 5(9): 1571-4, 2003 May 01.
Article in English | MEDLINE | ID: mdl-12713326

ABSTRACT

The reduction of allylic thiols to alkenes by hydrogen sulfide in aqueous solutions, a novel reaction that may explain reduction processes widely occurring in natural environments, has been discovered. Its mechanism has been studied and suggested to follow an S(RN)1-like pathway involving radical intermediates undergoing 1,4 hydrogen shifts. [reaction: see text]


Subject(s)
Allyl Compounds/chemistry , Hydrogen Sulfide/chemistry , Sulfhydryl Compounds/chemistry , Water Pollutants/analysis , Water/chemistry , Alkenes/chemistry , Free Radicals/chemistry , Hydrogen/chemistry , Isomerism , Oxidation-Reduction
12.
Chem Commun (Camb) ; (16): 1750-1, 2002 Aug 21.
Article in English | MEDLINE | ID: mdl-12196981

ABSTRACT

Two bridgehead-alkylated 2-thiaadamantanes (1,5-dimethyl and 1-methyl) have been identified in petroleum; these compounds give clues to sulfurisation processes affecting petroleum which has undergone high thermal stress.


Subject(s)
Amantadine/analogs & derivatives , Amantadine/chemistry , Petroleum/analysis , Sulfides/chemistry , Molecular Structure , Sulfur/chemistry , Temperature
13.
Chem Commun (Camb) ; (9): 944-5, 2002 May 07.
Article in English | MEDLINE | ID: mdl-12123060

ABSTRACT

A fruitful combination of potentiometry, absorption spectrophotometry, ESMS and 1H NMR enabled the characterisation of two caesium complexes with norbadione A and the determination of the respective stability constants of a mononuclear and a dinuclear caesium complex at pH approximately 6; a preliminary study allowed the assignment of five protonation sites of this pigment; a positively cooperative binding of the second Cs+ cation was observed.


Subject(s)
4-Butyrolactone/chemistry , Agaricales/metabolism , Phenylacetates/chemistry , 4-Butyrolactone/analogs & derivatives , 4-Butyrolactone/pharmacokinetics , Cesium Radioisotopes/pharmacokinetics , Kinetics , Magnetic Resonance Spectroscopy , Mass Spectrometry , Phenylacetates/pharmacokinetics , Potentiometry
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