Farzin Mohaya, Hassanpour Shahin, Zendehdel Morteza, Vazir Bita, Asghari Ahmad
Division of Physiology, Department of Basic Sciences, Faculty of Veterinary Medicine, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Division of Physiology, Department of Basic Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran 14155-6453, Iran.
IBRO Neurosci Rep. 2024 May 3;16:542-549. doi: 10.1016/j.ibneur.2024.04.010. eCollection 2024 Jun.
Complex homeostatic control mechanisms are tools to adjust the food birds eat and their appetite. Birds and mammals differ in several ways considering food intake regulation. Therefore, this study aimed to investigate the special effects of the intracerebroventricular (ICV) injection of spexin and its interaction with nitric oxide, serotonin and corticotropin receptors on central food intake regulation in broilers. In the test 1, Broilers received ICV injection of saline, PCPA (p-chlorophenylalanine,1.25 µg), spexin (10 nmol) and PCPA+spexin. In test 2-7, 8-OH-DPAT, SB-242084 (5-HT2C, 1.5 µg), L-arginine (Precursor of nitric oxide, 200 nmol), L-NAME (nitric oxide synthetize inhibitor, 100 nmol), Astressin-B (30 µg) and Astressin2-B (30 µg) were injected to Broilers instead of the PCPA. Then, the amount of food received was measured up to 2 h after the injection. The food consumption was significantly decreased by Spexin (10 nmol) (P<0.05). Concomitant injection of SB-242084+spexin attenuated spexin-induced hypophagia (P<0.05). Co-injection of L-arginine+spexin enhanced spexin-induced hypophagia and this effect was reversed by L-NAME (P<0.05). Also, concomitant injection of Astressin-B + spexin or Astressin2-B + spexin enhanced spexin-induced hypophagia (P<0.05). Founded on these observations, spexin-induced hypophagia may be mediated by nitric oxide and 5-HT2C, CRF1, and CRF2 receptors in neonatal broilers.
复杂的稳态控制机制是调节鸟类食物摄入量和食欲的工具。在食物摄入调节方面,鸟类和哺乳动物在几个方面存在差异。因此,本研究旨在探讨脑室内注射斯佩辛及其与一氧化氮、血清素和促肾上腺皮质激素受体的相互作用对肉鸡中枢食物摄入调节的特殊影响。在实验1中,肉鸡接受脑室内注射生理盐水、对氯苯丙氨酸(PCPA,1.25μg)、斯佩辛(10nmol)以及PCPA+斯佩辛。在实验2 - 7中,用8 - 羟基二丙胺基四氢萘(8 - OH - DPAT)、SB - 242084(5 - HT2C,1.5μg)、L - 精氨酸(一氧化氮前体,200nmol)、L - 硝基精氨酸甲酯(L - NAME,一氧化氮合成抑制剂,100nmol)、促肾上腺皮质激素释放因子拮抗剂B(Astressin - B,30μg)和促肾上腺皮质激素释放因子拮抗剂2 - B(Astressin2 - B,30μg)代替PCPA注射到肉鸡体内。然后,在注射后2小时内测量所摄入的食物量。斯佩辛(10nmol)显著降低了食物消耗量(P<0.05)。同时注射SB - 242084+斯佩辛减弱了斯佩辛诱导的摄食减少(P<0.05)。L - 精氨酸+斯佩辛共同注射增强了斯佩辛诱导的摄食减少,而这种作用被L - NAME逆转(P<0.05)。此外,同时注射Astressin - B +斯佩辛或Astressin2 - B +斯佩辛增强了斯佩辛诱导的摄食减少(P<0.05)。基于这些观察结果,斯佩辛诱导的摄食减少可能由新生肉鸡体内的一氧化氮以及5 - HT2C、促肾上腺皮质激素释放因子1(CRF1)和促肾上腺皮质激素释放因子2(CRF2)受体介导。