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Distribution and fate of DCX/PSA-NCAM expressing cells in the adult mammalian cortex： A local reservoir for adult cortical neuroplasticity？

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Frontiers in Biology 2016年第3期11卷 193-213页

作者： richard konig Bruno Benedetti Peter Rotheneichner Anna O' Sullivan Christina Kreutzer Maria Belles Juan Nacher Thomas M. Weiger Ludwig Aigner Sebastien Couillard-Despres Spinal Cord Injury and Tissue Regeneration Center Salzburg (SCI-TReCS) Paracelsus Medical University Salzburg Austria Institute of Molecular Regenerative Medicine Paracelsus Medical University Salzburg Austria Department of Physiology and Medical Physics Innsbruck Medical University Innsbruck Austria Institute of Experimental Neuroregenerat ion Paracelsus Medical University Salzburg Austria Department of Otorhinolaryngology Head and Neck Surgery Paracelsus Medical University Salzburg Salzburg Austria Neurobiology Unit Interdisciplinary Research Structure ffor Biotechnology and Biomedicine Valencia. Universitat de Valencia.Comunitat Valenciana Spain Division of Cellular and Molecular Neurobiology Department of Cell Biology University of Salzburg Salzburg Austria

Abstract The expression of early developmental markers such as doublecortin （DCX） and the polysialylated-neural cell adhesion molecule （PSA-NCAMIp has been used to identify immature neurons within canonical neurogenic niches. Additionally, DCX/PSA-NCAM ＋ immature neurons reside in cortical layer II of the paleocortex and in the paleo- and entorhinal cortex of mice and rats, respectively. These cells are also found in the neocortex of guinea pigs, rabbits, some afrotherian mammals, cats, dogs, non-human primates, and humans. The population of cortical DCX/PSA-NCAM ＋ immature neurons is generated prenatally as conclusively demonstrated in mice, rats, and guinea pigs. Thus, the majority of these cells do not appear to be the product of adult proliferative events. The immature neurons in cortical layer II are most abundant in the corlLices of young individuals, while very few DCX/PSA-NCAM ＋ cortical neurons can be detected in aged mammals. Maturation of DCX/PSA-NCAM ＋ cells into glutamatergic and GABAergic neurons has been proposed as an explanation for the age-dependent reduction in their population over time. In this review, we compile the recent information regarding the age-related decrease in the number of cortical DCX/PSA-NCAM ＋ neurons. We compare the distribution and fates of DCX/PSA-NCAM ＋ neurons among mammalian species and speculate their impact on cognitive function. To respond to the diversity of adult neurogenesis research produced over the last number of decades, we close this review by discussing the use and precision of the term ＂adult non-canonical neurogenesis.＂

关键词： aging cognition doublecortin piriform cortex plasticity neurogenesis

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Evaluation of Antimycobacterial Activity of Higenamine Using Galleria mellonella as an In Vivo Infection Model

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Natural Products and Bioprospecting 2018年第1期8卷 63-69页

作者： Paul Erasto richard Sunguruma Joan J.Munissi Victor Wiketye Charles de konig Atallah F.Ahmed National Institute for Medical Research P.O.Box 9653Dar Es SalaamTanzania Department of Chemistry University of Dar es SalaamDar Es SalaamTanzania School of Chemistry Witwatersrand UniversityJohannesburgRepublic of South Africa Department of Pharmacognosy College of PharmacyKing Saud UniversityP.O.Box 2457Riyadh 11451Saudi Arabia

The Phytochemical investigation on MeOH extract on the bark of Aristolochia brasiliensis Mart.&Zucc(Aristolochi-aceae)led to the isolation of major compound(1)as light brown grainy *** compound was identified as 1-(4-hydroxybenzyl)-1,2,3,4-tetrahydroisoquinoline-6,7-diol(higenamine)on the basis of spectroscopic analysis,including 1D and 2D NMR *** compound was evaluated for its antimycobacterial activity against Mycobacterium indicus pranii(MIP),using Galleria mellonella larva as an in vivo infection *** survival of MIP infected larvae after a single dose treatment of 100 mg/kg body weight of higenamine was 80%after 24 *** the compound exhibited a dose dependent activity,as evidenced by the reduction of colony density from 10^(5) to 10^(3) CFU for test concentrations of 50,100,150 and 200 mg/kg body weight *** IC50 value for higenamine was 161.6 mg/kg body weight as calculated from a calibration *** analysis showed that,a complete inhibition of MIP in the *** could be achieved at 334 mg/kg body *** the fact that MIP has been found to be highly resistant against isoniazid(INH)in an in vitro assay model,in this study the microbe was highly susceptible to this standard anti-TB *** isolation of higenamine from the genus Aristolochia and the method used to evaluate its in vivo antimycobacterial activity in *** are herein reported for the first time.

关键词： Aristolochia brasiliensis Galleria mellonella Higenamine Isoniazid Mycobacterium indicus pranii Antimycobacterial activity

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