New Knowledge On Why Patients With Type 2 Diabetes Present Smelling Problems
In a study in type 2 diabetic rats, researchers at the Karolinska Institutet have identified alterations in specific nerve cells that are important for odor identification. The findings might explain why type 2 diabetic patients often experience smelling problems and potentially open up a new research field to develop preventive therapies against neurodegenerative diseases in type 2 diabetic patients.
It is well known that patients with type 2 diabetes often suffer from neurodegenerative diseases such as Alzheimer’s disease. An early symptom of these neurodegenerative diseases is decreased odor identification ability. This kind of olfactory problem is also often present in patients with type 2 diabetes, suggesting that decreased smelling could be connected with the development of neurodegenerative diseases. However, so far, the nerve cells responsible for these smelling problems in type 2 diabetes have been unclear.
In the current study, published in the journal Oncotarget, researchers at the Karolinska Institutet identified alterations in a group of nerve cells called interneurons, in the piriform cortex of type 2 diabetic rats. The piriform cortex is a brain area that plays an essential role in odor identification and coding. The researchers also showed that the identified neuronal alterations could be counteracted pharmacologically by clinically used anti-diabetic drugs that mimic the mechanism of a hormone that enhances the production of insulin: the glucagon-like peptide 1.
“Neurodegenerative diseases are highly present within the type 2 diabetic population”, says Grazyna Lietzau, one of the researchers behind the study. “We believe that these findings could be important for the potential development of preventive pharmacological therapies against for example Alzheimer’s and Parkinson’s in these patients.”
This study is a result of a collaborative effort of researchers at Karolinska Institutet’s Department of Clinical Science and Education, Södersjukhuset (Cesare Patrone’s research group and Thomas Nyström), the Department of Molecular Medicine and Surgery, Karolinska Institutet (Claes-Göran Östenson), and the Department of Anatomy and Neurobiology, Medical University of Gdansk in Poland. The work was conceived and directed by Associate Professor Cesare Patrone and Dr Vladimer Darsalia, while Dr Grazyna Lietzau provided important scientific input and directed the experiments. Funders of the study were: the Swedish Heart-Lung foundation, Åhlén-stiftelsen, Stiftelsen för Gamla Tjänarinnor, Tornspiran Stiftelse and Konung Gustaf V:s & Drottning Victorias Frimurarestiftelse.
