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Amarante, M. K.

Publications and source records attributed to Amarante, M. K..

2 recordsLinked to original sources

Postinspiratory complex acts as a gating mechanism regulating swallow-breathing coordination and other laryngeal behaviors

Breathing needs to be tightly coordinated with upper airway behaviors, such as swallowing. Discoordination leads to aspiration pneumonia, the leading cause of death in neurodegenerative diseases. Here we study the role of the postinspiratory complex, (PiCo) in coordinating breathing and swallowing. Using optogenetic approaches in freely breathing-anesthetized ChATcre, Vglut2cre and co-transmission of ChATcre/Vglut2FlpO mice reveals this small brainstem microcircuit acts as a central gating mechanism for airway protective behaviors. Activation of PiCo during inspiration or the beginning of postinspiration triggers swallow behavior, while there is a higher probability for stimulating laryngeal activation when activated further into expiration, suggesting PiCos role in swallow-breathing coordination. PiCo triggers consistent swallow behavior and preserves physiologic swallow motor sequence, while stimulates laryngeal activation variable to stimulation duration. Sufficient bilateral PiCo activation is necessary for gating function since activation of only a few PiCo neurons or unilateral activation leads to blurred behavioral response. Viral tracing experiments reveal projections from the caudal nucleus of the solitary tract (cNTS), the presumed swallow pattern generator (SPG), to PiCo and vice versa. However, PiCo does not directly connect to laryngeal muscles. Investigating PiCos role in swallow and laryngeal coordination will aid in understanding discoordination in breathing and neurological diseases.

neuroscience↗

Association of the GIPR Glu354Gln (rs1800437) polymorphism with hypertension in a brazilian population

ObjectiveTo know the prevalence of the Glu354Gln polymorphism of the GIPR gene, investigate possible associations with arterial hypertension and relationships with cardiometabolic diseases.\n\nMethodA total of 311 subjects recruited from the Clinical Hospital of Londrina State University, located in a Brazilian metropolitan area. Random stratification was performed considering gender and geographic regions. Data were collected through interviews including anthropometric, sociodemographic and metabolic diseases related diseases. In order to analyze GIPR Glu354Gln gene polymorphism, polymerase chain reaction followed by followed by restriction fragment length polymorphism (PCR-RFLP) was performed.\n\nResultsThe highest prevalence for the allele C carriers were found in the Caucasian 29.4% (p = 0.043, OR = 1,89), hypertensive 37.1% (p < 0.0001), smokers 38.3% (p = 0.014) and dyslipidemic group 41.2% (p = 0.019). In this work 46.9% of the participants (n = 146) presented diseases related to cardiometabolic diseases. The results indicated that 60% of hypertensive patients (p = 0.004) and 64.7% of dyslipidemic patients (p = 0.046) were male. Among participants who presented cardiometabolic diseases, arterial hypertension was the most prevalent disease (71.9%), followed by obesity (43.8%). The family comorbidities history to cardiometabolic diseases (DM2, AH, dyslipidemia and obesity) had no significant association with the GIPR Glu354Gln genetic polymorphism. Although there was no difference in the case-control analyses for GIPR Glu354Gln for cardiometabolic group, regarding C allele carriers there were twice associated with arterial hypertension (p<0,001) and dyslipidemia (p<0,03).\n\nConclusionThe prevalence of the GIPR Glu354Gln for the CC genotype and for the C polymorphic allele was 25.7% and 3.2%, respectively. This study shows the potential participation of the GIPR Glu354Gln polymorphism with the pathophysiology of arterial hypertension, dyslipidemia in this Brazilian population. Taking into account the rarity of the CC genotype, additional studies with larger numbers of participants could contribute to a better understanding.

epidemiology↗