Al-Saadi Raghad, Mohammed Jawad Zainab Jamal, Khalaf Omar Hussein, Muhsain Siti Nur F
Department of Pathology & Poultry Diseases, College of Veterinary Medicine, University of Baghdad, Baghdad City, Iraq.
Faculty of Pharmacy, Universiti Teknologi MARA, Shah Alam, Malaysia.
Open Vet J. 2025 Jan;15(1):179-186. doi: 10.5455/OVJ.2025.v15.i1.17. Epub 2025 Jan 31.
Migraine is one of multiple attack neurological conditions that causes moderate to severe headaches with no defined pathophysiology and few animal models.
Establishing an animal model that reproduces migraine-like action is important in medical research to identify the mechanism underlying this disorder. Additionally, it facilitates the availability and reliability of new models that may act as human surrogate models.
Rabbits were divided into four groups. Negative group, migraine group, rizatriptan-nitroglycerin group, and rizatriptan group. The frequency of head scratching and the histopathological changes in the brain, liver, kidney, and heart for groups were evaluated in all groups.
The behavioral characteristic of head scratching was significantly increased in the NTG group (50.4 ± 3.8) compared with the control group (9.2 ± 1.3) after 30 min of the experiment. Moreover, animals treated with rizatriptan benzoate (Riza) 10 mg/kg/orally for 14 days followed by NTG injection showed a significant decrease in the head scratch action (16.8 ± 2.3 and 17.6 ± 3.3) than the animals of NTG group (50.4 ± 3.8 and 43.6 ± 2.3) after 30 min and 60 min, respectively. Furthermore, animals treated with Riza alone showed no statistical differences in the head scratches (7.8 ± 1.3, 9.2 ± 0.8, 10.6 ± 1.1 and 9.6 ± 1.3, respectively) during the 120 min of the experiment, compared with the control group. Histopathological alterations in the brain of rabbits that received NTG showed severe diffuse dilated and engorged blood vessels. These changes were also recorded in the liver and kidney of this group. This marked vasodilation of blood vessels and central and portal veins confirms the successful induction of migraine in the rabbit model. In contrast, animals treated with Riza for 14 days demonstrated substantially less vascular dilation following NTG injection. No significant pathological lesions were observed in animals treated with Riza.
The current study successfully established a rabbit model of migraine using a single dose of NTG to induce migraine-like behavior. Moreover, pre-treatment with rizatriptan benzoate for fourteen days significantly reduced the symptoms of migraine and histopathological changes in different organs.
偏头痛是一种发作性的神经系统疾病,可导致中度至重度头痛,其病理生理学尚不明确,动物模型也较少。
建立一种能重现偏头痛样作用的动物模型,对于医学研究中确定该疾病的潜在机制具有重要意义。此外,这有助于新模型的可用性和可靠性,这些新模型可作为人类替代模型。
将兔子分为四组。阴性组、偏头痛组、利扎曲普坦 - 硝酸甘油组和利扎曲普坦组。评估所有组兔子的挠头频率以及脑、肝、肾和心脏的组织病理学变化。
实验30分钟后,硝酸甘油组(50.4±3.8)挠头的行为特征相较于对照组(9.2±1.3)显著增加。此外,口服10mg/kg苯甲酸利扎曲普坦(利扎)14天,随后注射硝酸甘油的动物,在30分钟和60分钟后,挠头行为相较于硝酸甘油组动物(分别为50.4±3.8和43.6±2.3)显著减少(分别为16.8±2.3和17.6±3.3)。此外,在实验的120分钟内,单独使用利扎治疗的动物挠头情况(分别为7.8±1.3、9.2±0.8、10.6±1.1和9.6±1.3)与对照组相比无统计学差异。接受硝酸甘油的兔子脑部组织病理学改变显示血管严重弥漫性扩张和充血。该组的肝脏和肾脏也有这些变化。血管以及中央静脉和门静脉的这种明显血管扩张证实了在兔模型中成功诱导出偏头痛。相比之下,用利扎治疗14天的动物在注射硝酸甘油后血管扩张明显较少。用利扎治疗的动物未观察到明显的病理损伤。
本研究成功建立了一种使用单剂量硝酸甘油诱导偏头痛样行为的兔偏头痛模型。此外,用苯甲酸利扎曲普坦预处理14天可显著减轻偏头痛症状以及不同器官的组织病理学变化。