Scientists have discovered something relevant to people with type 1
or 2 diabetes, and it may lead to less diabetes related complications.
The discovery involves mitochondria in brain cells. Mitochondria are
cell organelles involved in respiration and energy production.
Researchers at the Yale School of Medicine determined that alterations
in the size of specific brain mitochondria play an essential role in
maintaining safe blood glucose levels.
“Low blood sugar can be as dangerous as high blood sugar,” said
researcher and Yale professor Sabrina Diano. “This new finding adds to
our understanding of how the body keeps blood sugar levels within a safe
range when sugar levels drop, like during fasting, or when they spike
after a meal.”
The Yale investigators were interested in understanding how the
brain’s appetite regulating neurons influence the body’s sugar levels.
Their study involved mice where the mitochondria protein called
dynamin-related protein 1 (DRP1) was either missing, or was present in
differing amounts in brain cells that detect circulating glucose.
It was discovered that, driven by the DRP1 protein, the mitochondria
changed its shape and size depending on whether a mouse was, or was not
hungry. “We found that when DRP1 activity in neurons was missing, these
neurons were more sensitive to changes in glucose levels,” said Diano.
The researchers were surprised that the observed intracellular
changes in such a small group of neurons were important for raising
blood sugar levels during fasting periods by activating a brain response
signaling organs such as the liver to step-up glucose production.
The study’s findings, according to Diano, imply that changes in this
mechanism may be involved in the development of hypoglycemia-associated
autonomic failure (HAAF), a diabetes complication that more often occurs
in those with type 1 diabetes.
HAAF is characterized by decreased symptom perception, or
hypoglycemia unawareness, and a diminished counter-regulatory hormone
response to low blood sugar. The Yale team plans to continue their
investigation by focusing on the role of mitochondria changes in the
development of HAAF.
Fonte: http://www.informationaboutdiabetes.com/news/diabetes-research/tiny-brain-organelles-influence-glucose-levels
Comentário do Bloguista: Diabetes
é uma doença crónica que surge quando o organismo não consegue
estabilizar os níveis de açúcar (glucose) no sangue. Os cientistas
descobriram algo relevante para as pessoas com diabetes tipo 1 ou 2.
A descoberta envolve mitocôndrias em células
cerebrais, pesquisadores da Faculdade de Medicina de Yale determinaram
que alterações no tamanho das mitocôndrias cerebrais específicas
desempenham um papel essencial na manutenção dos níveis seguros de
glicose no sangue. O estudo envolveu uma proteína das mitocôndrias, DRP1
(Dynamin-related protein 1), em diferentes quantidades em células
cerebrais que detectam a glicose circulante. Alterações intracelulares
observadas em um pequeno grupo de neurónios foram importantes para
elevar os níveis de açúcar no sangue durante os períodos de jejum,
ativando uma resposta do cérebro, sinalizando órgãos como o fígado para
aumentar a produção de glicose.
De acordo com o estudo
mudanças neste mecanismo podem estar envolvidas no desenvolvimento da
falha autonómica associada à hipoglicemia (HAAF), uma complicação que
ocorre mais frequentemente em diabéticos tipo 1.

The creation of this blog came from a challenge posed to Masters students of Biomedical Sciences of the University of Beira Interior, Covilhã (Portugal), by Professor Doctor José Eduardo Cavaco within the course "Project in Biomedical Sciences''.
The Biomedical Sciences combine the areas of Biology, Biochemistry, Physics, Management and Engineering, stimulating the capacity for self learning, critical thinking and adaptation to new technologies.
Thus, the Biomedics integration in different areas of the national and international job market is possible as technical supporters in clinical environment, consulting, industry, education and research.
For more information: http://www.ubi.pt/Curso/907.
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