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Volume 7, Issue 3 (Suppl)

J Nutr Disorders Ther, an open access journal

ISSN: 2161-0509

Page 95

JOINT EVENT

&

July 27-29, 2017 Rome, Italy

Advances in Natural Medicines Nutraceuticals & Neurocognition

14

th

International Conference on Clinical Nutrition

13

th

International Congress on

Intrauterine Growth Restriction (IUGR): a serotonergic neuropathologic picture in experimental

animals and human infants

Jorge Hernández–Rodríqguez

1

and

Gabriel Manjarreéz–Gutiérrez

2

1

Medicine University of Querétaro, México

2

National Institute of Social Security, México

I

n our lab, we evaluated if the free plasma fraction of L-Tryptophan (FFT) and the N1/P2 component of the auditory evoked

potentials (AEP) were associated with impaired brain serotonin neurotransmission in infant rats and humans with IUGR.

FFT, bound and total plasma L-Trp were measured and the AEP’s, in a prospective, longitudinal and comparative study,

comparing IUGR and control infants. Results showed that the FFT was increased and the amplitude of the N1/P2 component of

AEP was significantly decreased in IUGR relative to control infants. FFT and the N1/P2 component had a negative association.

We concluded that in newborns with IUGR, the changes in measured FFT and in the amplitude of N1/P2 component of

AEP, suggest an inverse association between FFT and the N1/P2 component of AEP and that these changes observed may be

causally related with brain serotonergic activity. In IUGR epigenetic factors such as nutritional stress induced disturbances in

brain serotonin metabolism and in serotonergic activity, identifiable postnatally through alterations in AEP cortical responses,

may have influenced brain cerebral sensory cortex development. These data allowed us to propose the presence of an impaired

serotonergic transmission, installed very early in brain development and that might be also casually associated with brain

serotonin-related disorders in adulthood.

jorgeh@webmail.fisio.cinvestav.mx

J Nutr Disorders Ther 2017, 7:3(Suppl)

DOI: 10.4172/2161-0509-C1-007

The science behind citicoline to protect against neurodegenerative processes and maintaining normal

cognitive function

Karen E Todd

Kyowa Hakko, USA

Statement of the Problem:

The human brain is under constant attack by various factors, including environmental pollution,

internal toxicity, stress and lack of nutrients due to poor diet. As we age, communication between neurons decreases and affects

memory, focus, attention, recall and mental energy. Critical to brain function is citicoline, or CDP choline. The compound is

comprised of cytidine and choline, with the former crucial for proper absorption of choline. In the brain, citicoline promotes

the production of phosphatidylcholine (phospholipids), which make up ~30% of brain tissue, aid in neural communication

and provide essential protection for neurons. The body obtains choline naturally through foods such as eggs and meat. But as

we age, the body loses some of its ability to absorb choline.

Methodology & Orientation:

Numerous scientific studies have shown that daily supplementation of citicoline may improve

brain function for subjects including healthy adolescent males, healthy middle-aged women and the elderly.

Findings:

Clinical trials have shown that a branded form of citicoline—Cognizin®—may be effective in combating the effects

of certain neurodegenerative processes. Studies also show Cognizin® may aid in maintaining normal cognitive function with

aging and point to its ability to act as an antioxidant in preserving normal healthy visual function. This form of citicoline has

been shown to protect neural tissue from the ravages of free radical damage and is the only form approved for use within

Europe as a dietary supplement ingredient.

todd@kyowa-usa.com