مقالات رزومه دکتر کیمیا مهدوی

Understanding the mechanism of food intake is important for comprehending energy balance, obesity, and the body weight regulation. In particular, examining birds' appetite is critical for conservation efforts, managing human-bird interactions, and understanding the environmental implications of bird feeding practices. In this systematic review, using the PRISMA guideline, we investigated the mediators that were identified as factors affecting the birds' appetite in 2022 and 2023. In order to obtain the appropriate studies, suitable keywords were searched in the relevant electronic databases and an anthology of the desired articles was done. According to the findings, the central administration of adrenomedullin, apelin-13, lipopolysaccharide, neuromedins and spexin causes hypophagia in chickens, while the injection of adiponectin, neuropeptide W (NPW) and phonexin-14 increased the food intake of birds. Also, regarding the members of RF-amide peptide family, neuropeptide VF (NPVF) and neuropeptide FF (NPFF) weakened the food consumption of birds, while kisspeptin and prolactin-releasing peptide (PrRP) strengthened it. The effects observed in birds were similar to mammals in most cases, indicating the structural and general similarities in the regulatory mechanisms of these strains, on the other hand, the contradictory effects between the two species were probably caused by genetic differences. Finally, despite the progress made in identifying the factors and mechanisms involved in regulating the appetite of birds, it is recommended to conduct future studies using modern laboratory methods, especially cellular-molecular methods.

According to previous studies, the serotonergic system plays a remarkable role in regulating meal intake, however, its role in the mediation of feeding caused by neuromodulin S (NMS) has not been investigated in birds. In the present research, 5 trials were considered in order to determine the links between these systems. In treatment 1, chickens received intracerebroventricular (ICV) infusion of NMS (0.25, 0.5, and 1 nmol). NMS (1 nmol), SB242084 (1.5 μg), a 5-HT2C receptor antagonist, and NMS + SB242084 were injected in the treatment 2. In subsequent treatments, instead of SB242084, 8-OH-DPAT (agonist of 5-HT1A receptor, 15.25 nmol), PCPA (serotonin synthesis inhibitor, 1.25 μg), and Fluoxetine (serotonin reuptake inhibitor, 10 μg) were applied. Then, total food consumption was recorded for 120 minutes. Based on observations, NMS dose-dependently attenuated meal intake (P<0.05). Hypophagia was diminished with NMS + SB242084 administration (P<0.05). ICV infusion of NMU + 8-OH-DPAT had no significant effect on the hypophagia (P≥0.05). The NMS-induced decreasing feed intake was attenuated with co-infusion of NMS+ PCPA (P< 0.05). Also, hypophagia was strengthened by NMS+ Fluoxetine co-infusion (P< 0.05). According to the results, the NMS-induced hypophagia is possibly mediated via 5-HT2c receptors in layer-type chickens.

Serotonin (5-HT) plays an underpinning role in appetite regulation and the opioid system has a role in the modulation of the ingestion behavior in birds. The current survey was aimed to evaluate the effect of opioid receptors on serotonin-induced hypophagia in neonatal broilers. During experiments, food-deprived chickens received intracerebroventricular (ICV) injection and thereafter, the cumulative food intake was measured after 30, 60, and 120 minutes. In experiment 1, to determine the effective dose of serotonin, the control solution and the various doses of serotonin (2.5, 5, and 10 μg) were administered to birds. In the second experiment, groups received not only the control solution, but also an effective dose of serotonin (10 µg), µ-opioid receptor antagonist (β_FNA, 5 µg), and a co-injection of β_FNA (5 µg) and serotonin (10 µg), respectively. The next experiments were similar to the second experiment, however, in place of β_FNA, the antagonist of κ- opioid receptor (nor_BNI, 5 µg), the δ- opioid receptor antagonist (NTI, 5 µg), and the agonist of µ opioid receptor (DAMGO, 62.25 pmol) were used in experiments 3, 4, and 5, respectively. The results showed a dose-dependent hypophagic impact of serotonin. This effect was attenuated by β_FNA; however, nor_BNI and NTI had no effect. Furthermore, the diminishing effect of serotonin on food consumption in chickens was strengthened following DAMGO administration (p < 0.05). According to the results, the hypophagic effect of serotonin is possibly mediated through µ opioid receptors in neonatal broilers.