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1.
Pharmacol Biochem Behav ; 227-228: 173587, 2023 06.
Article in English | MEDLINE | ID: mdl-37308040

ABSTRACT

Patterns of drug ingestion may have a dissimilar impact on the brain, and therefore also the development of drug addiction. One pattern is binge intoxication that refers to the ingestion of a high amount of drug on a single occasion followed by an abstinence period of variable duration. In this study, our goal was to contrast the effect of continuous low amounts with intermittent higher amounts of Arachidonyl-chloro-ethylamide (ACEA), a CB1R agonist, on amphetamine seeking and ingestion, and describe the effects on the expression of CB1R and CRFR1 in the central nucleus of the amygdala (CeA) and in the nucleus accumbens shell (NAcS). Adult male Wistar rats were treated with a daily administration of vehicle or 20 µg of ACEA, or four days of vehicle followed by 100 µg of ACEA on the fifth day, for a total of 30 days. Upon completion of this treatment, the CB1R and CRFR1 expression in the CeA and NAcS was evaluated by immunofluorescence. Additional groups of rats were evaluated for their anxiety levels (elevated plus maze, EPM), amphetamine (AMPH) self-administration (ASA) and breakpoint (A-BP), as well as AMPH-induced conditioned place preference (A-CPP). Results indicated that ACEA induced changes in the CB1R and CRFR1 expression in both the NAcS and CeA. An increase in anxiety-like behavior, ASA, A-BP and A-CPP was also observed. Since the intermittent administration of 100 µg of ACEA induced the most evident changes in most of the parameters studied, we concluded that binge-like ingestion of drugs induces changes in the brain that may make the subject more vulnerable to developing drug addiction.


Subject(s)
Amphetamine , Nucleus Accumbens , Rats , Male , Animals , Nucleus Accumbens/metabolism , Amphetamine/pharmacology , Rats, Wistar , Amygdala , Conditioning, Classical
2.
Data Brief ; 32: 106095, 2020 Oct.
Article in English | MEDLINE | ID: mdl-32793782

ABSTRACT

Within the variables relevant to the design of a pavement structure, the subgrade soils should be considered, which must be characterized in order to determine their mechanical properties and their bearing capacity. However, in developing countries such as Colombia, where the resources available for the design phase of a road project are very scarce, simplified and low-cost techniques should be used while delivering fast results, in order to be able to determine the geotechnical characteristics of soils. Therefore, it is necessary to look for correlations between the different geotechnical variables of subgrade soils. This document contains a database with the main physical characteristics of the soils. To collect these data, 46 geotechnical survey were carried out through several urban road sectors located in the city of Sincelejo, northern Colombia. Field tests were carried out with the Dynamic Cone Penetrometer and laboratory tests from undisturbed samples, for the realization of the California Bearing Ratio. Additionally, from disturbed samples, standard soil tests were conduct. The dataset obtained from the characterization of the soils, helps to create correlations between different variables, in such a way that it is possible to obtain bearing capacity parameters, such as CBR and Resilient Modulus, required for pavement design, based on simpler and faster tests such as the Dynamic Cone Penetrometer test, soil particle size analysis, the Atterberg limits or soil moisture content. In addition, these data can be supplemented by future researches in geographical regions with socioeconomic characteristics similar to those of Colombia.

3.
Front Pharmacol ; 11: 616630, 2020.
Article in English | MEDLINE | ID: mdl-33613283

ABSTRACT

Background: The identification of genetic risk factors for Acute Lymphoblastic Leukemia (ALL), are increasingly urgent and necessary. Objective: The purpose of this study is to determine the association of the genetic polymorphisms ABCC1 rs3743527, NCF4 rs1883112 and CBR3 rs1056892 with ALL. Methods: DNA samples were obtained in 71 children with ALL (from 2 to 18 years) and in 71 controls without ALL, to determine the polymorphisms by real-time polymerase chain reaction (qPCR), using specific TaqMan probes in a StepOne® thermal cycler (Applied Biosystems, United States). Results: The results of the Odds Ratio analysis show that in the rs1883112 polymorphism of the NCF4 gene, the heterozygous allele has a risk effect for ALL (OR = 3.1870, CI = 1.8880-7.9383 and p = 0.0002), in turn the mutated genotype (AA) is associated with a protective effect (OR = 0.26, 0.1248 to 0.5434 and p = 0.0003). On the other hand, the CBR3 rs1056892 polymorphism shows a significant association of risk to ALL, in the presence of the HT genotype (OR = 2.77, IC = 1.3837 to 5.5651 and p = 0.004) and the mutated genotype of this polymorphism has a significant association with protection to ALL in the HM genotype (OR = 0.52, IC = 0.2639 to 1.0304 and p = 0.05). While the inheritance models of the polymorphisms let us see that of the rs1883112 polymorphism of the NCF4 polymorphism; the HT genotype of the codominant model shows a protective effect against ALL (OR = 0.4117, IC = 0.1718 to 0.9866 and p = 0.04), the recessive model shows us and confirms what we already saw in table number 3, being that there is an association with protective effect in the HM genotype (OR = 0.2604, IC = 0.1248 to 0.5434 and p = 0.0003). In the polymorphism rs1056892 of the CBR3 gene, a protection association was found in the heterozygous allele of the codominant model (OR = 0.3448, IC = 0.1375 to 0.8896 and p = 0.0274). In addition, the recessive inheritance model for the HM genotype shows a protective effect to ALL, (OR = 0.52, CI = 0.9919 to 3.8638 and p = 0.05). Conclusion: There is an evident impact of the NCF4 rs1883112 and CBR3 rs1056892 polymorphisms with an increased risk of susceptibility to ALL; Likewise, through the codominant inheritance model, the effect of the variation of the CBR3 rs1056892 gene as a protective factor against ALL was evaluated.

4.
Auton Neurosci ; 205: 12-20, 2017 07.
Article in English | MEDLINE | ID: mdl-28254195

ABSTRACT

The application of sodium cyanide (NaCN) to the carotid body receptors (CBR) (CBR stimulation) induces rapid blood hyperglycemia and an increase in brain glucose retention. The commissural nucleus tractus solitarius (cNTS) is an essential relay nucleus in this hyperglycemic reflex; it receives glutamatergic afferents (that also release brain derived neurotrophic factor, BDNF) from the nodose-petrosal ganglia that relays CBR information. Previous work showed that AMPA in NTS blocks hyperglycemia and brain glucose retention after CBR stimulation. In contrast, BDNF, which attenuates glutamatergic AMPA currents in NTS, enhances these glycemic responses. Here we investigated the combined effects of BDNF and AMPA (and their antagonists) in NTS on the glycemic responses to CBR stimulation. Microinjections of BDNF plus AMPA into the cNTS before CBR stimulation in anesthetized rats, induced blood hyperglycemia and an increase in brain arteriovenous (a-v) of blood glucose concentration difference, which we infer is due to increased brain glucose retention. By contrast, the microinjection of the TrkB antagonist K252a plus AMPA abolished the glycemic responses to CBR stimulation similar to what is observed after AMPA pretreatments. In BDNF plus AMPA microinjections preceding CBR stimulation, the number of c-fos immunoreactive cNTS neurons increased. In contrast, in the rats microinjected with K252a plus AMPA in NTS, before CBR stimulation, c-fos expression in cNTS decreased. The expression of AMPA receptors GluR2/3 did not change in any of the studied groups. These results indicate that BDNF in cNTS plays a key role in the modulation of the hyperglycemic reflex initiated by CBR stimulation.


Subject(s)
Brain-Derived Neurotrophic Factor/metabolism , Carotid Body/drug effects , Carotid Body/metabolism , Hyperglycemia/metabolism , Solitary Nucleus/metabolism , alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid/metabolism , Animals , Brain-Derived Neurotrophic Factor/administration & dosage , Enzyme-Linked Immunosorbent Assay , Glucose/metabolism , Hyperglycemia/chemically induced , Hyperglycemia/pathology , Immunohistochemistry , Male , Microinjections , Neurotransmitter Agents/pharmacology , Proto-Oncogene Proteins c-fos/metabolism , Random Allocation , Rats, Wistar , Receptor, trkB/agonists , Receptor, trkB/antagonists & inhibitors , Receptor, trkB/metabolism , Receptors, AMPA/agonists , Receptors, AMPA/antagonists & inhibitors , Receptors, AMPA/metabolism , Sodium Cyanide/pharmacology , Solitary Nucleus/cytology , Solitary Nucleus/drug effects , alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid/administration & dosage
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