This site uses cookies to measure how you use the website so it can be updated and improved based on your needs and also uses cookies to help remember the notifications you’ve seen, like this one, so that we don’t show them to you again. If you could also tell us a little bit about yourself, this information will help us understand how we can support you better and make this site even easier for you to use and navigate.

Memantine prevents hypoglycemia-induced decrements of the cerebral energy status in healthy subjects

Authors

Willenborg, B., Schmoller, A., Caspary, J., Melchert, U. H., Scholand-Engler, H. G., Jauch-Chara, K., Hohagen, F., Schweiger, U., Oltmanns, K. M.

Journal

The Journal Of Clinical Endocrinology And Metabolism, Volume: 96, No.: 2, Pages.: E384-E388

Year of Publication

2011

Abstract

Context: The risk to develop dementia is significantly increased in diabetes mellitus. Memantine, an N-methyl-D-aspartate receptor antagonist, which is clinically applied in dementia, has been shown to exert neuroprotective effects under hypoglycemic conditions in rats.; Objective: We hypothesized that memantine may prevent hypoglycemia-induced decrements in the cerebral high-energy phosphate, i.e. ATP, metabolism to exert its neuroprotective action under these conditions.; Design and Participants: In a randomized, double-blind crossover design, we applied memantine vs. placebo in 16 healthy male subjects and examined the cerebral high-energy phosphate metabolism by (31)phosphor magnetic resonance spectroscopy, hormonal counterregulation, and neurocognitive performance during hypoglycemic glucose clamp conditions.; Results: We found increments in hormonal counterregulation and reduced neurocognitive performance during hypoglycemia (P < 0.05). Cerebral ATP levels increased upon hypoglycemia in the memantine condition as compared with placebo (P = 0.006) and remained higher after renormalizing blood glucose concentrations (P = 0.018), which was confirmed by ATP to inorganic phosphate ratio (P = 0.046). Phosphocreatine levels and phosphocreatine to inorganic phosphate ratio remained stable throughout the experiments and did not differ between conditions (P > 0.1 for both).; Conclusion: Our data demonstrate that memantine preserves the cerebral energy status during experimentally induced hypoglycemia in healthy subjects. An improved neuronal energy status may thus be involved in the neuroprotective effect under these conditions and may qualify memantine as potential future option to combat cognitive impairments and dementia in diabetes.;

Bibtex Citation

@article{Willenborg_2011, doi = {10.1210/jc.2010-1348}, url = {http://dx.doi.org/10.1210/jc.2010-1348}, year = 2011, month = {feb}, publisher = {The Endocrine Society}, volume = {96}, number = {2}, pages = {E384--E388}, author = {B. Willenborg and A. Schmoller and J. Caspary and U. H. Melchert and H. G. Scholand-Engler and K. Jauch-Chara and F. Hohagen and U. Schweiger and K. M. Oltmanns}, title = {Memantine Prevents Hypoglycemia-Induced Decrements of the Cerebral Energy Status in Healthy Subjects}, journal = {The Journal of Clinical Endocrinology {&} Metabolism} }

Keywords

adenosine triphosphate, adult, blood, blood glucose, brain chemistry, diabetes, dizocilpine maleate, double-blind method, drug effects, energy metabolism, glucose clamp technique, hormones, humans, hyperinsulinism, hypoglycemia, insulin, magnetic resonance imaging, male, memantine, metabolism, neuroprotective agents, pharmacology, phosphorus isotopes, prevention & control, stroop test, young adult

Countries of Study

Germany

Types of Study

Before and After Study

Type of Interventions

Risk Factor Modification

Risk Factor Modifications

At risk population