屠宰时不同程度β受体刺激对猪背最长肌钙蛋白酶-钙pastatin系统活性的影响

P. L. Sensky, T. Parr, R. Bardsley, P. Buttery
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引用次数: 1

摘要

尽管努力使育种、营养和饲养制度标准化,但消费者研究表明,在英国销售的所有里脊排中,17%在韧性和干燥度方面是不可接受的(Warkup等人,1995年)。最近的证据表明,这种无法解释的变异可能至少部分是由于屠宰前后钙蛋白酶-钙pastatin蛋白水解系统的变化,这是由天然β-激动剂肾上腺素循环水平的变化所刺激的(Sensky等,1996)。屠宰时钙pastatin(系统的抑制成分)的增加也被证明与嫩化程度降低有关(Koohmaraie, 1992, Sensky等人,1996b)。因此,接近屠宰时β受体刺激程度的变化应该与屠宰时的钙pastatin水平相关。本研究旨在调查这一说法的有效性。在屠宰前16小时,将30头雌性长×大白猪(67±1 kg)的饲粮中分别添加2或20 ppm的β拮抗剂纳多洛尔或20 ppm的β激动剂克仑特罗,分为5组,每组6头猪,包括对照组(不添加纳多洛尔),分别给予从低(20 ppm纳多洛尔)到高(20 ppm克仑特罗)不同程度的β受体刺激。在屠宰后立即采用色谱和荧光技术测量背最长肌(LD)样品中的钙蛋白酶和钙pastatin活性(Sensky等,1996b)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of varying the degrees of β-receptor stimulation on the activity of the calpain - calpastatin system at slaughter in porcine longissimus dorsi
Despite efforts to standardise breeding, nutrition and husbandry regimes, consumer studies indicate that 17% of all loin chops sold in the UK are unacceptable in terms of toughness and dryness (Warkup et al., 1995). Recent evidence suggests that this unaccountable variability may be at least partly due to changes in the calpain-calpastatin proteolytic system around the time of slaughter, stimulated by changes in the circulating levels of the natural β-agonist adrenaline (Sensky et al., 1996). An increase in calpastatin, the inhibitory component of the system, at slaughter has also been shown to be associated with reduced degrees of tenderisation (Koohmaraie, 1992, Sensky et al., 1996b). Variation in the degree of β-receptor stimulation close to slaughter should therefore correlate with calpastatin levels at slaughter. This study aimed to investigate the validity of this claim.The diet of 30 female Landrace x Large White pigs (67 ± 1 kg) was supplemented with either 2 or 20 ppm nadolol, a β-antagonist, or clenbuterol, a β-agonist, 16 h before slaughter, giving 5 groups of 6 pigs, including controls (no supplement), with differing degrees of β-receptor stimulation, ranging from low (20 ppm nadolol) to high (20 ppm clenbuterol). Calpain and calpastatin activities were measured in samples of longissimus dorsi (LD) taken immediately after slaughter using chromatographic and fluorimetric techniques (Sensky et al., 1996b).
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