Sub-Chronic Agmatine Administration Dose-Dependently Increased Learning and Memory As Well As Social Interaction In Healthy Rats


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Bozkurt N. M., Beyaz F., Kıryar B., Ünal G.

5th International Congress on Psychopharmacology & Child and Adolescent Psychopharmacology / Psychotherapy (ICP 2024), Antalya, Türkiye, 22 - 25 Nisan 2024, ss.79

  • Yayın Türü: Bildiri / Özet Bildiri
  • Basıldığı Şehir: Antalya
  • Basıldığı Ülke: Türkiye
  • Sayfa Sayıları: ss.79
  • Erciyes Üniversitesi Adresli: Evet

Özet

BACKGROUND AND AIM: Agmatine, synthesized as a result of the decarboxylation of l-arginine by

arginine decarboxylase, is an endogenous polyamine. Agmatine as a neuromodulator of the central nervous

system; G proteins interact with many molecular targets such as protein kinases, GABAergic receptors,

glutamatergic receptors, imidazoline receptors, alpha2-adrenergic receptors, voltage-gated calcium channels

and nitric oxide synthase. Agmatine, which shows its biological effects in the central nervous system by


interacting with specific receptors and neuronal pathways, has shown neuroprotective, anti-

neuroinflammatory and memory modulating effects in cellular and animal models of central nervous system


disorders. However, the effects of agmatine on learning-memory and social interaction of healthy animals

are unclear. In this study, we investigated the effects of chronic agmatine administration on rats' visual spatial

learning and memory, as well as their effects on social interaction.

METHODS: 10-week-old rats were used in our study, and the rats were randomly divided into four groups

(n = 8 for each group): Saline, Agmatine (40 mg/kg), Agmatine (80 mg/kg) and Agmatine (120 mg/kg). All

treatments were administered daily intraperitoneally for twenty eight days. Behavioral experiments were

performed from the twenty-first day of treatments. Novel object recognition test was used to test visual

learning and memory in rats, Y-maze test was used to test spatial learning and memory, and social interaction

test was performed to test social interaction.

RESULTS: Agmatine (40 mg/kg) and Agmatine (80 mg/kg) increased visual learning and memory, spatial

learning and memory, and social interaction in rats compared to the control group. Agmatine (120 mg/kg)

impaired visual learning and memory, as well as spatial learning and memory, in rats compared to the control

group. Agmatine (120 mg/kg) did not alter social interaction in rats.

CONCLUSIONS: Our study showed that sub-chronic agmatine administration in healthy rats can increase

learning and memory in a dose-dependent manner. It has also been shown that sub-chronic agmatine

administration increases social interaction in healthy rats. While these effects of agmatine can be attributed

to its being a multimodal neuromodulator, further studies are needed to elucidate its mechanism of action.