Buczko W, Dziaczkowski J, Kopec M, Moniuszko-Jakoniuk J, Sopata I, Wisniewski K, Wize J, Wojtecka-Lukasik E
Br J Pharmacol. 1980 Aug;69(4):551-4. doi: 10.1111/j.1476-5381.1980.tb07902.x.
1 Collagen degradation products (CDP) resulting from bacterial collagenase digestion were fractionated by gel filtration and their biological activities in rats were estimated. 2 CDP induced the following kinin-like effects: increase in permeability of skin blood vessels, contraction of the isolated intestine of the rat, depression of locomotor activity and of motor coordination. 3 The most active CDP fraction was CDP III containing peptides of mol. wt. < 1000 D with a high percentage of hydroxyproline. 4 As compared with bradykinin, CDP III was less active in the skin permeability test and was 15,000 to 20,000 fold less effective in induction of isolated intestine contraction. 5 Depression of the CNS induced by 30 microgram of CDP III administered into the brain ventricle was similar to that observed after 4 microgram of bradykinin given by the same route. 6 CDP III prolonged the duration of sleep evoked by thiopentone and enhanced the threshold of convulsion induced by pentazol. 7 The activity of CDP in comparison to other low molecular weight peptides is discussed.
对细菌胶原酶消化产生的胶原降解产物(CDP)进行凝胶过滤分级,并评估其在大鼠体内的生物活性。
CDP诱导了以下类激肽效应:皮肤血管通透性增加、大鼠离体肠管收缩、运动活性和运动协调性降低。
活性最强的CDP组分是CDP III,其含有分子量<1000 D的肽,且羟脯氨酸含量很高。
与缓激肽相比,CDP III在皮肤通透性试验中的活性较低,诱导离体肠管收缩的效力低15000至20000倍。
向脑室注射30微克CDP III诱导的中枢神经系统抑制与经相同途径给予4微克缓激肽后观察到的情况相似。
CDP III延长了硫喷妥钠诱发的睡眠时间,并提高了戊唑诱发惊厥的阈值。
讨论了CDP与其他低分子量肽相比的活性。