Biochemistry & Pharmacology: Open Access
Open Access
ISSN: 2167-0501
+44-77-2385-9429
ISSN: 2167-0501
+44-77-2385-9429
Sinan Cavun, Gulce Sevdar, M Sertac Yilmaz, Levent R Buyukuysal and Sami Aydin
Uludag University, Turkey
Posters & Accepted Abstracts: Biochem Pharmacol (Los Angel)
Statement of the Problem: Depression is the 4th leading cause of disability and death all around the world and it is expected
to be be the 2nd cause after 2020. Globally, more than 300 million people of all ages suffer from depression. The high rate of
patients who still have not responded to depression treatment makes it necessary to perform preclinical research. The current
medications used in depression treatment are also very troublesome drugs in respect of the adverse effects they cause. The risks
and adverse effects of antidepressants currently used for depression treatment spread in a large range from sexual problems to
death. In the current brain microdialysis studies from our laboratory, it is shown that glycyl-glutamine (Gly-Gln) augments
serotonin release in the brain. It is well known that serotonin is a hormone that makes people feel happy, energetic and lively. In
this study, we aim to investigate antidepressant effects of Gly-Gln dipeptide because of its enhancing effects on serotonin levels.
Methodology: These studies have been performed by the "forced swimming test" method which is the most applied animal
model used in antidepressant treatment surveys. Using the swimming test, the dose response study, comparison with Gly-Gln
cleavage products and fluoxetine, as well as locomotor activity test was performed.
Findings: In this sense, animal studies performed with â??glycyl-glutamineâ? showed that it is tremendously effective against
depression.
Conclusion: The most important feature of Gly-Gln is being a molecule, which can be synthesized in our body endogenously,
and it is comes off while ?²-endorphin is being burned in the body. Therefore, Gly-Gln is extremely safe with its adverse effects.
There isnâ??t any adverse effect observed during the toxicological studies. This result is important for considering Gly-Gln as a
potential antidepressant.
Recent Publications
1. M Guclu, S Kiyici, Z Gul and S Cavun (2017) Exenatide treatment causes suppression of serum fasting ghrelin levels in
patients with type 2 diabetes mellitus. Endocrine Connections EC-17-0242.
2. N F Basaran, R L Buyukuysal, M S Yilmaz, S Aydin, S Cavun, et al. (2016) The effect of Glyâ??Gln [??-endorphin 30â??31]
on morphine-evoked serotonin and GABA efflux in the nucleus accumbens of conscious rats. Neuropeptides 58:23â??29.
3. S Kiyici, N F Basaran, S Cavun and V Savci (2015) Central injection of CDP-choline suppresses serum ghrelin levels
while increasing serum leptin levels in rats. European Journal of Pharmacology 764:264â??270.
4. N F Basaran, R L Buyukuysal, W R Millington and S Cavun (2010) Glycyl-
5. glutamine (?²-endorphin30-31) inhibits morphine-induced dopamine efflux in the nucleus accumbens. Naunyn-
Schmiedeberg's Archives of Pharmacology, 381(5):467â??475.
6. S Cavun, G G?¶ktalay and W R Millington (2005) Glycyl-glutamine, an endogenous ?²-endorphin-derived peptide, inhibits
morphine-induced conditioned place preference, tolerance, dependence, and withdrawal. Journal of Pharmacology and
Experimental Therapeutics 315(2):949â??958.
Sinan Cavun, after graduating from the Uludag University, Faculty of Medicine in 1993, completed his Doctoral Education in 1999. He has been working in the field of Pharmacology for a total of 17 years. He worked for eight years in Hospital Medicine Management as a Team Leader. He has focused on neuropharmacology, particularly on depression and neuroendocrine regulation. As a result of his work, he has a European patent in this regard (use of Gly-Gln in the treatment of depression).
E-mail: scavun@uludag.edu.tr