Mushtaq Saima, Das Yavuz Kursad, Aksoy Abdurrahman
Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, Ondokuz Mayis University, Samsun, Türkiye.
Vet Med Sci. 2025 Jan;11(1):e70190. doi: 10.1002/vms3.70190.
This study aimed to compare the inhibitory effect of flunixin meglumine and meloxicam on the smooth muscles of the gastrointestinal tract in male cattle. Tissue samples, including the abomasum, ileum, proximal loop and centripetal gyri of the ascending colon, were collected from routinely slaughtered male cattle. These samples were sectioned into strips and mounted in an isolated tissue bath system. Smooth muscle contractions were evoked using carbachol, and cumulative doses of atropine, flunixin meglumine and meloxicam were administered to assess smooth muscle activity. Atropine, used as a positive control, did not abolish contractions in the abomasum and centripetal gyri tissues, even at a high concentration of 10 µM. Based on area-under-curve values, flunixin meglumine demonstrated a greater inhibitory effect than meloxicam by factors of 8.57, 4.28, 12.44 and 3.93 in the abomasum, ileum, proximal loop and centripetal gyri tissues, respectively. For beats-per-minute values, flunixin meglumine exhibited a stronger inhibitory effect than meloxicam by factors of 7.22, 3.88, 7.03 and 3.35 in the abomasum, ileum, proximal loop and centripetal gyri tissues, respectively. Finally, based on peak maximum values, flunixin meglumine's inhibitory effect was 6.13, 4.43, 7.07 and 7.02 times greater than that of meloxicam in the abomasum, ileum, proximal loop and centripetal gyri tissues, respectively. In conclusion, flunixin meglumine was more potent than meloxicam in inhibiting smooth muscle activity. Conversely, meloxicam is associated with fewer adverse effects due to its selective action on the cyclooxygenase-2 enzyme. However, flunixin meglumine may be more advantageous than meloxicam for applications in beef and milk production due to its shorter residue elimination time.
本研究旨在比较氟尼辛葡甲胺和美洛昔康对雄性牛胃肠道平滑肌的抑制作用。从常规屠宰的雄性牛中采集组织样本,包括皱胃、回肠、升结肠近端袢和向心回。将这些样本切成条带并安装在离体组织浴系统中。使用卡巴胆碱诱发平滑肌收缩,并给予累积剂量的阿托品、氟尼辛葡甲胺和美洛昔康以评估平滑肌活性。用作阳性对照的阿托品,即使在高浓度10 µM时,也不能消除皱胃和向心回组织中的收缩。基于曲线下面积值,氟尼辛葡甲胺在皱胃、回肠、近端袢和向心回组织中分别比美洛昔康表现出大8.57、4.28、12.44和3.93倍的抑制作用。对于每分钟搏动值,氟尼辛葡甲胺在皱胃、回肠、近端袢和向心回组织中分别比美洛昔康表现出强7.22、3.88、7.03和3.35倍的抑制作用。最后,基于峰值最大值,氟尼辛葡甲胺在皱胃、回肠、近端袢和向心回组织中的抑制作用分别比美洛昔康大6.13、4.43、7.07和7.02倍。总之,氟尼辛葡甲胺在抑制平滑肌活性方面比美洛昔康更有效。相反,美洛昔康因其对环氧化酶-2酶的选择性作用而副作用较少。然而,由于氟尼辛葡甲胺的残留消除时间较短,在牛肉和牛奶生产中的应用可能比美洛昔康更具优势。