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1.
Purinergic Signal ; 17(2): 255-271, 2021 06.
Article in English | MEDLINE | ID: mdl-33834349

ABSTRACT

Ischemic stroke is a major cause of morbidity and mortality worldwide and only few affected patients are able to receive treatment, especially in developing countries. Detailed pathophysiology of brain ischemia has been extensively studied in order to discover new treatments with a broad therapeutic window and that are accessible to patients worldwide. The nucleoside guanosine (Guo) has been shown to have neuroprotective effects in animal models of brain diseases, including ischemic stroke. In a rat model of focal permanent ischemia, systemic administration of Guo was effective only when administered immediately after stroke induction. In contrast, intranasal administration of Guo (In-Guo) was effective even when the first administration was 3 h after stroke induction. In order to validate the neuroprotective effect in this larger time window and to investigate In-Guo neuroprotection under global brain dysfunction induced by ischemia, we used the model of thermocoagulation of pial vessels in Wistar rats. In our study, we have found that In-Guo administered 3 h after stroke was capable of preventing ischemia-induced dysfunction, such as bilateral suppression and synchronicity of brain oscillations and ipsilateral cell death signaling, and increased permeability of the blood-brain barrier. In addition, In-Guo had a long-lasting effect on preventing ischemia-induced motor impairment. Our data reinforce In-Guo administration as a potential new treatment for brain ischemia with a more suitable therapeutic window.


Subject(s)
Brain/physiopathology , Guanosine/administration & dosage , Guanosine/therapeutic use , Ischemic Stroke/drug therapy , Ischemic Stroke/physiopathology , Neuroprotective Agents/administration & dosage , Neuroprotective Agents/therapeutic use , Administration, Intranasal , Animals , Blood-Brain Barrier/drug effects , Cell Death/drug effects , Cerebral Veins/drug effects , Electrocoagulation , Electroencephalography/drug effects , Functional Laterality/drug effects , Ischemic Stroke/complications , Male , Movement Disorders/etiology , Movement Disorders/prevention & control , Rats , Rats, Wistar , Signal Transduction/drug effects
2.
Mol Genet Metab ; 109(1): 33-40, 2013 May.
Article in English | MEDLINE | ID: mdl-23562162

ABSTRACT

Since we previously observed that in patients with mucopolysaccharidosis (MPS) the storage of undegraded glycosaminoglycans (GAG) occurs from birth, in the present study we aimed to compare normal, untreated MPS I mice (knockout for alpha-l-iduronidase-IDUA), and MPS I mice treated with enzyme replacement therapy (ERT, Laronidase, 1.2mg/kg every 2 weeks) started from birth (ERT-neo) or from 2 months of age (ERT-ad). All mice were sacrificed at 6 months. Both treatments were equally effective in normalizing GAG levels in the viscera but had no detectable effect on the joint. Heart function was also improved with both treatments. On the other hand, mice treated from birth presented better outcomes in the difficult-to-treat aortas and heart valves. Surprisingly, both groups had improvements in behavior tests, and normalization of GAG levels in the brain and IDUA injection resulted in detectable levels of enzyme in the brain tissue 1h after administration. ERT-ad mice developed significantly more anti-IDUA-IgG antibodies, and mice that didn't develop antibodies had better performances in behavior tests, indicating that development of antibodies may reduce enzyme bioavailability. Our results suggest that ERT started from birth leads to better outcomes in the aorta and heart valves, as well as a reduction in antibody levels. Some poor vascularized organs, such as the joints, had partial or no benefit and ancillary therapies might be needed for patients. The results presented here support the idea that ERT started from birth leads to better treatment outcomes and should be considered whenever possible, a observation that gains relevance as newborn screening programs are being considered for MPS and other treatable lysosomal storage disorders.


Subject(s)
Enzyme Replacement Therapy , Glycosaminoglycans/metabolism , Iduronidase/genetics , Mucopolysaccharidosis I/therapy , Animals , Brain/enzymology , Brain/pathology , Disease Models, Animal , Female , Genetic Vectors , Glycosaminoglycans/genetics , Humans , Iduronidase/administration & dosage , Iduronidase/metabolism , Lysosomes/enzymology , Lysosomes/pathology , Mice , Mice, Knockout , Mucopolysaccharidosis I/enzymology , Mucopolysaccharidosis I/genetics
3.
Metab Brain Dis ; 28(2): 187-92, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23111918

ABSTRACT

Hepatic encephalopathy (HE) arises from acute or chronic liver diseases and leads to cognitive deficits. Different animal models for the study of HE have demonstrated learning and memory impairment and a number of neurotransmitter systems have been proposed to be involved in this. Recently, it was described that bile duct-ligated (BDL) rats exhibited altered spatio-temporal locomotor and exploratory activities and biosynthesis of neurotransmitter GABA in brain cortices. Therefore, the aim of this study was to evaluate cognition in the same animal model. Male adult Wistar rats underwent common bile duct ligation (BDL rats) or manipulation of common bile duct without ligation (control rats). Six weeks after surgery, control and BDL rats underwent object recognition behavioral task. The BDL rats developed chronic liver failure and exhibited a decreased discrimination index for short term memory (STM) when compared to the control group. There was no difference in long term memory (LTM) as well as in total time of exploration in the training, STM and LTM sessions between the BDL and control rats. Therefore, the BDL rats demonstrated impaired STM for recognition memory, which was not due to decreased exploration.


Subject(s)
Bile Ducts/physiology , Hepatic Encephalopathy/psychology , Memory Disorders/chemically induced , Memory Disorders/psychology , Memory, Short-Term/physiology , Ammonia/blood , Animals , End Stage Liver Disease/psychology , Hepatic Encephalopathy/etiology , Hyperammonemia/blood , Hyperammonemia/etiology , Ligation , Male , Psychomotor Performance/physiology , Rats , Rats, Wistar , Recognition, Psychology/physiology , Synaptic Transmission/physiology
4.
Surg Endosc ; 25(8): 2637-42, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21416181

ABSTRACT

BACKGROUND: This study was designed to evaluate the effectiveness of barrier methods to prevent adhesions in videolaparoscopy, comparing the use of Surgicel(®) and Interceed(®) with the control group. METHODS: We performed a controlled, randomized study in healthy adult female rabbits Oryctolagus cuniculu, inducing adhesions in the abdominal wall by resection of a peritoneal fragment and cauterization. In the control group, surgery was performed, and the other group was randomized to the use of the barrier method. After 21 days, videolaparoscopy was repeated, and the presence or absence of adhesions and their score were verified by performing biopsies of the surgical site in all groups. RESULTS: No statistical differences were found in the results on adhesion formation and adhesions score among the three groups. In the control group, there were 54.5% cases of adhesion formation; the median score of adhesions was 6 (range, 3-10). In the Surgicel(®) group, there were 45.5% cases of adhesion formation; median score of adhesions was 6 (range, 4-10). In the Interceed(®) group, there were 45.5% cases of adhesion formation; median score of adhesions was 5 (range, 3-11). CONCLUSIONS: No difference was found using barrier methods, Surgicel(®), and Interceed(®) for preventing adhesion formation in videolaparoscopy.


Subject(s)
Cellulose, Oxidized , Laparoscopy/adverse effects , Laparoscopy/methods , Tissue Adhesions/prevention & control , Video-Assisted Surgery , Animals , Female , Pelvis , Rabbits
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