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  • 1
    Publication Date: 2013-03-02
    Description: Prenatal infection and exposure to traumatizing experiences during peripuberty have each been associated with increased risk for neuropsychiatric disorders. Evidence is lacking for the cumulative impact of such prenatal and postnatal environmental challenges on brain functions and vulnerability to psychiatric disease. Here, we show in a translational mouse model that combined exposure to prenatal immune challenge and peripubertal stress induces synergistic pathological effects on adult behavioral functions and neurochemistry. We further demonstrate that the prenatal insult markedly increases the vulnerability of the pubescent offspring to brain immune changes in response to stress. Our findings reveal interactions between two adverse environmental factors that have individually been associated with neuropsychiatric disease and support theories that mental illnesses with delayed onsets involve multiple environmental hits.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Giovanoli, Sandra -- Engler, Harald -- Engler, Andrea -- Richetto, Juliet -- Voget, Mareike -- Willi, Roman -- Winter, Christine -- Riva, Marco A -- Mortensen, Preben B -- Feldon, Joram -- Schedlowski, Manfred -- Meyer, Urs -- New York, N.Y. -- Science. 2013 Mar 1;339(6123):1095-9. doi: 10.1126/science.1228261.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Physiology and Behavior Laboratory, Swiss Federal Institute of Technology (ETH) Zurich, 8603 Schwerzenbach, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23449593" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cytokines/immunology ; Disease Models, Animal ; Female ; Humans ; Mental Disorders/*immunology ; Mice ; Mice, Inbred C57BL ; Poly I-C/immunology/pharmacology ; Pregnancy ; Prenatal Exposure Delayed Effects/*immunology/virology ; Puberty/*immunology ; Stress, Physiological/*immunology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 3940-3946 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Condensed Isoquinolines, IV. Syntheses with 3-Bromo- and 3-Hydrazino-s-triazolo[3.4-a]isoquinoline3-Bromo-s-triazolo[3.4-a]isoquinoline (2) or the unsubstituted s-triazolo[3.4-a]isoquinoline react with butyl lithium to afford the 3-lithio compound 4, which is stable at -70° and decomposes like the MgBr-salt at room temperature with cleavage of the triazolo ring to form l-aminoisoquinoline. From 2 and anthranilic acid 13-oxo-13H-isoquino[1′.2′ : 3.4]-s-triazolo[5.1-b]quinazoline (13) is obtained. N-acyl derivatives of 3-hydrazino-s-triazolo[3.4-a]iso-quinoline (14) cannot be cyclocondensed. 14 reacts with ethyl pyruvate to give via hydrazone 19 11-oxo-10-methyl-11H-as-triazino[4′.3′ : 1.5]-s-triazolo[3.4-a]isoquinoline (20). The thermal decomposition of 3-azido-s-triazolo[3.4-a]isoquinoline (22) in aniline leads to the phenylazo-derivative 23.
    Notes: Aus 3-Brom-s-triazolo[3.4-a]isochinolin (2) oder dem unsubstituierten s-Triazolo[3.4-a]isochinolin und Butyllithium entsteht die bei -70° stabile 3-Lithium-Verbindung 4, die wie das MgBr-Salz 3 bei Raumtemperatur unter Spaltung des Triazolringes in 1-Amino-isochinolin übergeht. Aus 2 und Anthranilsäure wird 13-Oxo-13H-isochino[1′.2′ : 3.4]-s-triazolo[5.1-b]-chinazolin (13) bereitet. N-Acyl-Derivate von 3-Hydrazino-s-triazolo[3.4-a]isochinolin (14) lassen sich nicht cyclokondensieren. 14 liefert mit Brenztraubensäureester via Hydrazon 19 das 11-Oxo-10-methyl-1 1H-as-triazino[4′.3′:1.5]-s-triazolo[3.4-a]isochinolin (20). Der thermische Zerfall von 3-Azido-s-triazolo[3.4-a]isochinolin (22) in Anilin führt zum Benzolazo-Derivat 23.
    Type of Medium: Electronic Resource
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