Ertbjerg P, Henckel P, Karlsson A, Larsen L M, Møller A J
Department of Dairy and Food Science, Royal Veterinary and Agricultural University, Frederiksberg C, Denmark.
J Anim Sci. 1999 Sep;77(9):2428-36. doi: 10.2527/1999.7792428x.
The objective of the study was to improve the understanding of the relationship between the effect of epinephrine plus exercise and meat tenderness. The calpain, calpastatin, and cathepsin B + L activities and postmortem proteolysis in porcine longissimus muscle were studied. The muscle glycogen stores were depleted in five pigs by s.c. injection of epinephrine (.3 mg/kg) at 15 h antemortem and exercise on a treadmill (5 min, 3.8 km/h) immediately before slaughter. Antemortem injection of epinephrine and treadmill exercise resulted in higher ultimate pH (6.32 vs 5.66 in control) and decreased (P < .05) thaw loss, cooking loss, and shear force values. The muscle energy depletion treatment increased (P < .05) the muscle mu-calpain activity measured 42 min postmortem, and at 24 h mu-calpain activity was still approximately 50% greater in the high ultimate pH group. Also, as the ratio of mu-calpain to calpastatin increased (P < .01), the overall proteolytic potential of the calpain system were greater. These observations suggest that the muscle energy level may influence the activity of the calpain system in the living animal. The high ultimate pH group showed lower (P < .001) cathepsin B + L activity in the myofibrillar and the soluble fractions after 8 d of storage, suggesting that the increased ultimate pH increased the stability of the lysosomal membrane and thereby reduced the release of cathepsins from the lysosomes during storage. The SDS-PAGE showed increased (P < .001) degradation of a 39-kDa band in the epinephrine and exercise-treated samples. Degradation products at 30, 31, and 32 kDa were labeled by troponin-T antibody in western blot. An appearing 24-kDa band was identified as a troponin-I degradation product in western blot. The proteolytic degradation pattern of myofibrillar proteins during storage differed in control and treated samples, supporting the hypothesis that calpain-mediated proteolysis was affected after treatment, resulting in meat with high ultimate pH.
本研究的目的是增进对肾上腺素加运动的效果与肉嫩度之间关系的理解。对猪的背最长肌中的钙蛋白酶、钙蛋白酶抑制蛋白以及组织蛋白酶B + L的活性和宰后蛋白水解情况进行了研究。在宰前15小时,通过皮下注射肾上腺素(0.3毫克/千克)使五头猪的肌肉糖原储备耗尽,并在屠宰前立即在跑步机上运动(5分钟,3.8千米/小时)。宰前注射肾上腺素和跑步机运动导致最终pH值升高(对照为5.66,处理组为6.32),解冻损失、烹饪损失和剪切力值降低(P < 0.05)。肌肉能量耗尽处理使宰后42分钟时测得的肌肉μ-钙蛋白酶活性增加(P < 0.05),在24小时时,高最终pH值组的μ-钙蛋白酶活性仍比对照组高约50%。此外,随着μ-钙蛋白酶与钙蛋白酶抑制蛋白的比例增加(P < 0.01),钙蛋白酶系统的整体蛋白水解潜力更大。这些观察结果表明,肌肉能量水平可能会影响活体动物中钙蛋白酶系统的活性。高最终pH值组在储存8天后,肌原纤维和可溶部分中的组织蛋白酶B + L活性较低(P < 0.001),这表明最终pH值升高增加了溶酶体膜的稳定性,从而减少了储存期间组织蛋白酶从溶酶体中的释放。SDS - PAGE显示,肾上腺素和运动处理组样品中一条39 kDa条带的降解增加(P < 0.001)。在蛋白质印迹中,30、31和32 kDa的降解产物被肌钙蛋白 - T抗体标记。在蛋白质印迹中,一条出现的24 kDa条带被鉴定为肌钙蛋白 - I降解产物。对照和处理样品在储存期间肌原纤维蛋白的蛋白水解降解模式不同,支持了处理后钙蛋白酶介导的蛋白水解受到影响,从而导致最终pH值较高的肉的假说。