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Featured researches published by L. Pinto.


Biomaterials | 2013

Chitosan tubes of varying degrees of acetylation for bridging peripheral nerve defects

Kirsten Haastert-Talini; Stefano Geuna; Lars B. Dahlin; Cora Meyer; Lena Stenberg; Thomas Freier; Claudia Heimann; Christina Barwig; L. Pinto; Stefania Raimondo; Giovanna Gambarotta; Silvina Ribeiro Samy; Nuno Sousa; António J. Salgado; Andreas Ratzka; Sandra Wrobel; Claudia Grothe

Biosynthetic nerve grafts are desired as alternative to autologous nerve grafts in peripheral nerve reconstruction. Artificial nerve conduits still have their limitations and are not widely accepted in the clinical setting. Here we report an analysis of fine-tuned chitosan tubes used to reconstruct 10 mm nerve defects in the adult rat. The chitosan tubes displayed low, medium and high degrees of acetylation (DAI: ≈ 2%, DA: ≈ 5%, DAIII: ≈ 20%) and therefore different degradability and microenvironments for the regenerating nerve tissue. Short and long term investigations were performed demonstrating that the chitosan tubes allowed functional and morphological nerve regeneration similar to autologous nerve grafts. Irrespective of the DA growth factor regulation demonstrated to be the same as in controls. Analyses of stereological parameters as well as the immunological tissue response at the implantation site and in the regenerated nerves, revealed that DAI and DAIII chitosan tubes displayed some limitations in the support of axonal regeneration and a high speed of degradation accompanied with low mechanical stability, respectively. The chitosan tubes combine several pre-requisites for a clinical acceptance and DAII chitosan tubes have to be judged as the most supportive for peripheral nerve regeneration.


Journal of The Peripheral Nervous System | 2012

BIOHYBRID – Biohybrid templates for peripheral nerve regeneration

Claudia Grothe; Kirsten Haastert-Talini; Thomas Freier; Xavier Navarro; Lars B. Dahlin; António J. Salgado; Shimon Rochkind; Abraham Shahar; L. Pinto; Martin Hildebrandt; Stefano Geuna

Dear Editor, Peripheral nerve injuries represent a major cause for morbidity and disability in affected patients and cause substantial costs for society in a global perspective. It has been estimated that peripheral nerve injuries affect 2.8% of trauma patients, many of whom acquire life-long disability (Noble et al., 1998). With respect to an incidence of nerve injuries of 13.9/100,000 inhabitants per year (Asplund et al., 2009) and the number of inhabitants in the EU (495,000,000 inhabitants in 2007), the number of peripheral nerve injuries requiring repair and reconstruction, excluding nerve injuries by amputations, may be 70,000 annually only in EU countries. Related to peripheral nerve injuries, the costs for society are substantial and consist of direct (costs for surgery, outpatient visits and rehabilitation) and indirect (lost production) costs. Individual median and ulnar nerve injuries in the forearm have total costs of EUR 51,000 and 31,000, respectively, where around 85% of the costs consist of loss of production (Rosberg et al., 2005), still excluding costs for adjusted quality of life (Eriksson et al., 2011). Thus, one may estimate that the annual costs only in the EU may be as high as EUR 2.2 billion, indicating that improved treatment strategies for peripheral nerve injuries may not only improve the situation for patients, but may also significantly reduce costs for society. Based on these premises, the EU granted EUR 6,000,000 fund as part of the seventh Framework Program to the BIOHYBRID consortium that was built with the overall aim to develop, in a pre-clinical perspective, an innovative biohybrid artificial nerve device for improving the regenerative treatment of severe traumatic injuries of peripheral nerves. BIOHYBRID is a 4-year collaborative project that started on October 1, 2011, and involves 10 partners from 5 European Countries (Germany, Italy, Portugal,


European Neuropsychopharmacology | 2017

Exploring the astrocytic neuroprotective functions in a chronic mild stress model of depression

J. Correia; P. Patricio; N.D. Alves; A.R. Santos; M. Morais; A. Mateus-Pinheiro; S. Guerra-Gomes; V.M. Sardinha; G. Tavares; M. Martins; Nuno Sousa; L. Pinto; João Filipe Oliveira

.................................................................................................................................. VII Resumo .................................................................................................................................... IX Table of contents ...................................................................................................................... XI Abbreviations list ..................................................................................................................... XV


European Neuropsychopharmacology | 2016

Cell cycle regulation of the hippocampal progenitor cells in an animal model of depression and after fluoxetine treatment

P. Patricio; A. Mateus-Pinheiro; A.R. Machado-Santos; N.D. Alves; M. Morais; João Bessa; Nuno Sousa; L. Pinto


European Neuropsychopharmacology | 2017

Tau-dependent suppression of adult neurogenesis in the stressed hippocampus

Chrysoula Dioli; P. Patricio; R. Trindade; L.G. Pinto; Joana Silva; M. Morais; Elisabete Ferreiro; S. Borges; A. Mateus-Pinheiro; A.J. Rodrigues; Nuno Sousa; João Bessa; L. Pinto; Ioannis Sotiropoulos


European Neuropsychopharmacology | 2017

AP2gamma transcription factor as a modulator of hippocampal neurogenesis in an animal model of depression

E. Loureiro-Campos; N.D. Alves; A. Mateus-Pinheiro; P. Patricio; A.R. Machado-Santos; Nuno Sousa; L. Pinto


European Neuropsychopharmacology | 2017

Chronic stress targets adult hippocampal neurogenesis preferentially in the suprapyramidal blade of rat dorsal dentate gyrus

N.D. Alves; P. Patricio; J. Correia; A. Mateus-Pinheiro; A.R. Machado-Santos; E. Loureiro-Campos; M. Morais; João Bessa; Nuno Sousa; L. Pinto


European Neuropsychopharmacology | 2017

The role of AP2gamma transcription factor in the modulation of adult glutamatergic neurogenesis in depression

E. Loureiro-Campos; N.D. Alves; A. Mateus-Pinheiro; P. Patricio; A.R. Machado-Santos; Nuno Sousa; L. Pinto


European Neuropsychopharmacology | 2017

Tau protein as a key element in stress-induced dendritic atrophy and suppression of adult hippocampal neurogenesis

Chrysoula Dioli; João Bessa; L. Pinto; Nuno Sousa; Ioannis Sotiropoulos


European Neuropsychopharmacology | 2016

The cytoskeletal protein Tau as a key element in stress-induced suppression of adult hippocampal neurogenesis

Chrysoula Dioli; R. Trindade; M. Morais; S. Borges; P. Patricio; A. Mateus-Pinheiro; L.G. Pinto; A.J. Rodrigues; Nuno Sousa; João Bessa; L. Pinto; Ioannis Sotiropoulos

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