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Research Project: Exploiting Nutrition and Protein Quality Controls to Delay Age-related Macular Degeneration and Cataracts

Location: Jean Mayer Human Nutrition Research Center On Aging

Title: Dietary starch composition effects on Cx43-intercellular communication channels and short-term memory

Author
item FRANCISCO, SARAH - Jean Mayer Human Nutrition Research Center On Aging At Tufts University
item SMITH, KELSEY - Jean Mayer Human Nutrition Research Center On Aging At Tufts University
item ROWAN, SHELDON - Jean Mayer Human Nutrition Research Center On Aging At Tufts University
item ARAGONES BARGALLO, GEMMA - Jean Mayer Human Nutrition Research Center On Aging At Tufts University
item SMITH, DONALD - Jean Mayer Human Nutrition Research Center On Aging At Tufts University
item Shukitt-Hale, Barbara
item TAYLOR, ALLEN - Jean Mayer Human Nutrition Research Center On Aging At Tufts University
item BEJARANO FERNANDEZ, ELOY - Jean Mayer Human Nutrition Research Center On Aging At Tufts University

Submitted to: Current Developments in Nutrition
Publication Type: Abstract Only
Publication Acceptance Date: 3/23/2020
Publication Date: 5/29/2020
Citation: Francisco, S., Smith, K., Rowan, S., Aragones Bargallo, G., Smith, D.E., Shukitt Hale, B., Taylor, A., Bejarano Fernandez, E. 2020. Dietary starch composition effects on Cx43-intercellular communication channels and short-term memory. Current Developments in Nutrition. 4(2):1205. https://doi.org/10.1093/cdn/nzaa057_021.
DOI: https://doi.org/10.1093/cdn/nzaa057_021

Interpretive Summary:

Technical Abstract: OBJECTIVES: Intercellular communication mediated by gap junctions is critical for cognitive and sensory functions and is disturbed with age and age-related diseases. We analyzed the impact of consuming a high glycemic diet or a low glycemic dietary intervention on Cx43, a component of gap junction intercellular communication channels associated with spatial short-term memory, in different age groups of mice. METHODS: Male C57Bl6/J mice (n = 12-13) aged 7 months were fed equal amounts of either a high glycemic (HG) diet or a low glycemic (LG) diet for 1 month or 9 months. Within the 9-month feeding trial, half of the HG-fed animals were switched to the LG diet (HGxLG) at 4.5 months. The diets are isocaloric, but the HG starch is 100% composed of amylopectin, and the LG diet contains a 30% amylopectin/70% amylose mixture of starch and is digested much slower. We also analyzed tissues from a previous feeding trial where 12-month aged animals were fed these same diets over 12 months. The animals were weighed weekly, underwent intraperitoneal glucose tolerance tests to evaluate glycemic response, were tested for cognition using a novel object recognition test, and tissues were collected. Tissues including brain and eye samples were evaluated for Cx43, a component of gap junction intercellular communication channels, using immunohistochemistry and western blotting. RESULTS: At both time points, compared to the LG-fed controls, the HG-fed animals had significantly increased (>10%) body weight, while the HGxLG crossover animals' body weight did not differ significantly from the LG-fed controls at 15 months. At 14 months, there was no significant difference in novel object recognition, although there was a trend of improved novel object recognition in the HGxLG crossover group. Cx43 gap junction protein accumulated in eye tissues of the HG-fed animals, and this accumulation was attenuated in the HGxLG group. CONCLUSIONS: These results suggest that detrimental consequences of a high glycemic diet during aging on cognitive function may be reversible, supporting that a switch in dietary habits may be an effective nutritional intervention in older adults.