Enhancing adult hippocampal neurogenesis with lysophosphatidic acid: a proposal for erasing cocaine contextual memory

Stimulating adult hippocampal neurogenesis (AHN) has been uncovered as a promising approach in the manipulation of retrograde memories. This work aims to study whether increasing AHN with lysophosphatidic acid (LPA, an endogenous lysophospholipid with proneurogenic actions) promotes the forgetting of previously established cocaine-contextual associations. C57BL/6J mice previously trained in a cocaine-induced conditioned place preference (CPP) paradigm were submitted to 23 days of withdrawal, during which they received repeated intracerebroventricular infusions of LPA, ki16425 (a selective LPA1/3 receptors antagonist), or vehicle solution. Then, CPP maintenance was assessed, and the causal role of AHN in this process was evaluated using a mediation analysis. In a complementary experiment, wild-type and LPA1-null mice were acutely infused with LPA or ki16425 to determine the involvement of the LPA1 receptor in the in vivo proneurogenic actions of LPA. The chronic LPA treatment significantly weakened the long-term retention of a previously acquired cocaine-CPP memory, an effect clearly mediated by a LPA-induced increase in the number of adult-born dentate granule cells. In contrast, the ki16425-treated mice displayed aberrant responses of initially decreased CPP retention that progressively increased CPP across the extinction sessions, in absence of effects on AHN. The histological studies suggested that the proneurogenic actions of LPA were related to the enhancement of cell proliferation and critically depended on the LPA1 receptor function. Our results suggest that the LPA/LPA1-pathway acts as a potent in vivo modulator of AHN, and highlight the usefulness of a post-learning increase of adult-born hippocampal neurons as a strategy to promote the forgetting of cocaine-context associations.Plan Propio de Investigación y Transferencia. Campus de Excelencia Internacional Andalucía Tech. Spanish Ministry of Economy and Competitiveness (Agencia Estatal de Investigación), co‐funded by the European Research Development Fund (AEI/FEDER, UE) (PSI2013‐44901‐P and PSI2017‐82604‐R to L.J.S. and PSI2015‐73156‐JIN to E.C.O.); by the National System of Health‐Instituto de Salud Carlos III, which is co‐funded by AEI/FEDER, UE (Red de Trastornos Adictivos; RD16/0017/0001 to F.R.d.F.); and by the Andalusian R&D&I Programme, Regional Ministry of Economy and Knowledge (PAIDI CTS643 to G.E.T.). D.L.G.M. hold a FPU grant from the Spanish Ministry of Education, Culture and Sports (FPU13/04819 ). F.R.d.F. and G.E.T. are supported by Nicolas Monardes Programme, from the Andalusian Regional Ministry of Health. E.C.O. holds a ‘Jóvenes Investigadores’ grant (code: PSI2015‐73156‐JIN) from the Spanish Ministry of Economy and Competitiveness (Agencia Estatal de Investigación), which is co‐funded by the AEI/FEDER, UE

More adult-born dentate gyrus neurons to weaken cocaine-related retrograde memories: an in vivo strategy employing exogenous lysophosphatidic acid

The post-training enhancement of adult hippocampal neurogenesis (AHN) has been receiving growing interest as a potential method to manipulate retrograde memories. Recent hypothesis suggest that the addition of adult-born dentate granule cells might promotes remodeling of pre-existing hippocampal circuits, which might both clear cocaine-related memories and facilitate the learning of new adaptive information. Here, we study the effect of stimulating AHN in vivo with exogenous lysophosphatidic acid (LPA) on the maintenance of retrograde cocaine-contextual associative memories. Male C57BL/6J mice trained in a cocaine-induced Conditioned Place Preference (CPP) model were later submitted to repeated intracerebroventricular (i.c.v.) injections of LPA, Ki16425 or vehicle solution during withdrawal. Afterwards, the long-term persistence of the cocaine-CPP was assessed and the mediational role of AHN in this process was evaluated. In addition, wild-type and mice lacking the LPA1 receptor received a single i.c.v. injection of LPA, Ki16425 or vehicle to assess the role of the LPA1 receptor in the LPA-induced increase of AHN. Our results revealed that the chronic administration of LPA decreased the retention of a previously acquired cocaine-induced CPP. This effect was mediated by an LPA-induced increase of AHN. In contrast, mice treated with Ki16425 showed reduced cocaine-CPP retention, but they increased their preference for the cocaine-paired compartment throughout CPP extinction. Besides, no effects of Ki16425 on AHN were found. Immunohistochemical studies suggested that LPA stimulated cell proliferation and promoted neuronal maturation with a key role of the LPA1 receptor. These findings emphasize the relevance of LPA and its LPA1 receptor as an in vivo modulator of AHN and the utility of the post-training increase of adult-born hippocampal neurons to weaken cocaine-context associations.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tec

Degree Recital: Jeremy Ahn

Jeremy Ahn, piano, presents his Senior Degree recital. Performing works by Bach, Mussorgsky, and Kapustin.https://digitalcommons.andrews.edu/seniors-2020-2021/1002/thumbnail.jp

Training memory without aversion: Appetitive hole-board spatial learning increases adult hippocampal neurogenesis.

Learning experiences are potent modulators of adult hippocampal neurogenesis (AHN). However, the vast majority of findings on the learning-induced regulation of AHN derive from aversively-motivated tasks, mainly the water maze paradigm, in which stress is a confounding factor that affects the AHN outcome. Currently, little is known regarding the effect of appetitively-motivated training on AHN. Hence we studied how spatial learning to find food rewards in a hole-board maze modulates AHN (cell proliferation and immature neurons) and AHN-related hippocampal neuroplasticity markers (BDNF, IGF-II and CREB phosphorylation) in mice. The 'Trained' mice were tested for both spatial reference and working memory and compared to 'Pseudotrained' mice (exposed to different baited holes in each session, thus avoiding the reference memory component of the task) and 'Control' mice (exposed to the maze without rewards). In contrast to Pseudotrained and Control mice, Trained mice reduced the number of proliferating hippocampal cells but they notably increased their population of immature neurons assessed by immunohistochemistry. This evidence shows that hole-board spatial reference learning diminishes cell proliferation in favor of enhancing young neurons' survival. Interestingly, the enhanced AHN in the Trained mice (specifically in the suprapyramidal blade) positively correlated with their reference memory performance, but not with their working memory. Furthermore, the Trained animals increased the hippocampal protein expression of all the neuroplasticity markers analyzed by western blot. Results show that the appetitively-motivated hole-board task is an useful paradigm to potentiate and/or investigate AHN and hippocampal plasticity minimizing aversive variables such as fear or stress.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech. This study was funded by grants from the Spanish Ministry of Economy and Competitiveness (Agencia Estatal de Investigación) co-funded by the European Research Development Fund -AEI/FEDER, UE- (PSI2015-73156-JIN ‘Jóvenes Investigadores grant’ to E.C.O. and PSI2013-44901-P to L.J.S. and C.P.), from ‘Junta de Andalucía’ SEJ1863 to C.P. and from University of Málaga (Plan Propio 2017 – ‘Ayudas para proyectos puente’) to M.G.F. Author P.S.P. holds a ‘Juan de la Cierva-formación‘grant from the Spanish Ministry of Economy, Industry and Competitiveness (code: FJCI-2015-23925) and a ‘D.3. Estancia de investigadores de reconocido prestigio en la UMA‘ grant from the University of Málaga. Authors R.D.M.F. and D.L.G.M. hold ‘FPU’ grants from the Spanish Ministry of Education, Culture and Sports (code: FPU14-01610 and FPU13/04819, respectively). Author F.J.P. holds a ‘Miguel Servet’ grant (code: CP14/00212) from the National System of Health-Instituto de Salud Carlos-III co-funded by FEDER, UE

A note on constrained degree reduction of polynomials in Bernstein–Bézier form over simplex domain

AbstractIn the paper [H.S. Kim, Y.J. Ahn, Constrained degree reduction of polynomials in Bernstein–Bézier form over simplex domain, J. Comput. Appl. Math. 216 (2008) 14–19], Kim and Ahn proved that the best constrained degree reduction of a polynomial over d-dimensional simplex domain in L2-norm equals the best approximation of weighted Euclidean norm of the Bernstein–Bézier coefficients of the given polynomial. In this paper, we presented a counterexample to show that the approximating polynomial of lower degree to a polynomial is virtually non-existent when d≥2. Furthermore, we provide an assumption to guarantee the existence of solution for the constrained degree reduction

Vivian Raimundo Senior Voice Recital

Vivian Raimundo, soprano gives her senior recital performance accompanied by Jeremy Ahn, pianist (and guitarist).https://digitalcommons.andrews.edu/seniors-2020-2021/1012/thumbnail.jp