Research output: Contribution to journal › Article › peer-review
The STin2VNTR Polymorphism of the Serotonin Transporter Protein: Association with the Efficiency of Short-Term Memory in Young and Elderly Subjects. / Volf, N. V.; Privodnova, E. Yu; Bazovkina, D. V.
In: Neuroscience and Behavioral Physiology, Vol. 50, No. 6, 01.07.2020, p. 695-699.Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - The STin2VNTR Polymorphism of the Serotonin Transporter Protein: Association with the Efficiency of Short-Term Memory in Young and Elderly Subjects
AU - Volf, N. V.
AU - Privodnova, E. Yu
AU - Bazovkina, D. V.
PY - 2020/7/1
Y1 - 2020/7/1
N2 - Cognitive abilities and the rate of their extinction with age are shown to be determined to a significant extent by genetic factors. The serotoninergic system of the brain affects the development and plastic rearrangements of the brain, and plays an important role in learning and memory processes. Links found between the activity of the serotonin transporter gene and the efficiency of memory processes provided grounds for studying associations between the efficiency of memory and the STin2VNTR polymorphism, which results from a change in the number of tandem repeats in intron 2, which has two frequent alleles (10 and 12 repeats) and one rare (nine repeats) allele. This polymorphism fulfils the role of an allele-dependent amplifier of gene expression. The studies involved younger (n = 204: 84 men and 120 women, age 19–35 years) and older (n = 129: 57 men and 72 women, age over 55 years) right-handed subjects. The efficiency of verbal memory was determined in terms of reproduction of words heard with the right and left ears in a dichotic test procedure and in terms of a measure of the recognition, among distractors, of syllables previously displayed on a screen; imaginal memory efficiency was tested in terms of shape recognition. Regardless of other factors, carriers of the 12/12 genotype of the STin2VNTR polymorphism, as compared with carriers of the 10 allele, demonstrated significantly better memorization of dichotically presented words and imaginal memory. For imaginal memory, the genotype effect was more marked in the older age group.
AB - Cognitive abilities and the rate of their extinction with age are shown to be determined to a significant extent by genetic factors. The serotoninergic system of the brain affects the development and plastic rearrangements of the brain, and plays an important role in learning and memory processes. Links found between the activity of the serotonin transporter gene and the efficiency of memory processes provided grounds for studying associations between the efficiency of memory and the STin2VNTR polymorphism, which results from a change in the number of tandem repeats in intron 2, which has two frequent alleles (10 and 12 repeats) and one rare (nine repeats) allele. This polymorphism fulfils the role of an allele-dependent amplifier of gene expression. The studies involved younger (n = 204: 84 men and 120 women, age 19–35 years) and older (n = 129: 57 men and 72 women, age over 55 years) right-handed subjects. The efficiency of verbal memory was determined in terms of reproduction of words heard with the right and left ears in a dichotic test procedure and in terms of a measure of the recognition, among distractors, of syllables previously displayed on a screen; imaginal memory efficiency was tested in terms of shape recognition. Regardless of other factors, carriers of the 12/12 genotype of the STin2VNTR polymorphism, as compared with carriers of the 10 allele, demonstrated significantly better memorization of dichotically presented words and imaginal memory. For imaginal memory, the genotype effect was more marked in the older age group.
KW - aging
KW - memory
KW - STin2VNTR polymorphism of the serotonin transporter gene
UR - http://www.scopus.com/inward/record.url?scp=85090122109&partnerID=8YFLogxK
U2 - 10.1007/s11055-020-00957-4
DO - 10.1007/s11055-020-00957-4
M3 - Article
AN - SCOPUS:85090122109
VL - 50
SP - 695
EP - 699
JO - Neuroscience and Behavioral Physiology
JF - Neuroscience and Behavioral Physiology
SN - 0097-0549
IS - 6
ER -
ID: 25309368