Molecular Sciences III. Posters
Körmendi, Petra
Department of Medical Chemistry, Molecular Biology and Pathobiochemistry
+36302495687
petra.bianka.kormendi@gmail.com
Effect of Ethanol Exposure on Longevity and Chemotaxis on Caenorhabditis Elegans
Körmendi Petra, Cynthia Hunn, Gábor Hajdú, and Csaba Barta
Semmelweis University
Department of Medical Chemistry, Molecular Biology and Pathobiochemistry
Molecular Sciences III. Posters
Hungarian
Molecular Sciences
Neurosciences
Alcohol is one of the most frequently abused addictive substances in humans, which has a wide range of effects on the central nervous system. About 70% of C. elegans genes are homologous to those of humans and a resemblance between the nervous systems of the two species can clearly be pointed out: Dopaminergic as well as serotonergic neurons are present in their central nervous systems, which play a role in the reward system and are indispensable when discussing addiction. Both dopamine and serotonin affect movement and behavior of the animals. The fully mapped out neuronal network and the precise knowledge of the functionality of its synapses makes C. elegans a valuable model for addiction research.
In the longevity paradigm C. elegans was treated with 400mM and 200mM ethanol from day one adult age onwards. In the diacetyl race paradigm animals were conditioned to 400mM and 200mM ethanol for 24 hours during late L4-young adult state, and after 1 hour withdrawal period transferred to a race plate (infused with or without ethanol) and subjected to an attractive odorant stimulus (diacetyl).
High dose ethanol reduces lifespan by almost 50%, whereas low dose has either no, or considerably effect on longevity. Upon alcohol treatment, the worm’s characteristic movements are also altered. In diacetyl race after high dose treatment (400mM), the worms may lose the ability to coordinate their movement, orientation or their interest towards the attractant diacetyl. Upon lower dosage, these responses were less prevalent. Wild type (N2) animals were compared to serotonin deficient (tryptophane-hydroxylase) tph-1-, and dopamine receptor deficient dop-2 (ortholog of human DRD2) null mutants.
Our results have shown that alcohol induces changes in C. elegans longevity as well as behavior in a dose dependent manner. High concentration ethanol exposure decreases life span dramatically and hinders locomotor performance that can be at least partially rescued by low dose exposure during the race. Neurotransmitter deficient mutants also showed alterations in motility patterns. A further advantage of the worm model is the possibility of examining transgenerational and epigenetical effects.
Supervisor:
Barta Csaba
barta.csaba@med.semmelweis-univ.hu
Poszter
Szabad
elfogadva
poszter
nem rendelkezett róla
4752
11:10
11:13
Körmendi Petra, Cynthia Hunn, Gábor Hajdú, and Csaba Barta
Semmelweis University
Department of Medical Chemistry, Molecular Biology and Pathobiochemistry