Telegdy G, Kádár T, Kovács K, Penke B
Life Sci. 1984 Jul 9;35(2):163-70. doi: 10.1016/0024-3205(84)90135-8.
The effects of intraperitoneally (ip.) and intracerebroventricularly (icv.) administered sulfated and nonsulfated cholecystokinin octapeptide (CCK-8-SE and CCK-8-NS) and their N- and C-terminal fragments on the tail-pinch-induced feeding behavior of rats were investigated. After ip. administration, only CCK-8-SE inhibited tail-pinch-induced food intake. After icv. administration, both CCK-8-SE and CCK-8-NS, in doses of 800 pmole/rat, reduced the amount of food eaten. Of the CCK fragments tested icv., the sulfated N-terminal fragments, the middle portion of the CCK-8-sequence (the CCK-3-6 fragment), and the C-terminal tetrapeptide depressed the food intake of rats during tail-pinch, whereas the C-terminal tripeptide significantly increased it. The results suggest that CCK peptides inhibit tail-pinch-induced feeding by separate mechanisms, depending on the route of administration.
研究了腹腔内(ip.)和脑室内(icv.)注射硫酸化和非硫酸化的胆囊收缩素八肽(CCK - 8 - SE和CCK - 8 - NS)及其N端和C端片段对大鼠尾部夹捏诱导的摄食行为的影响。腹腔注射后,只有CCK - 8 - SE抑制尾部夹捏诱导的食物摄入。脑室内注射后,剂量为800 pmole/大鼠的CCK - 8 - SE和CCK - 8 - NS均减少了食物摄入量。在脑室内注射测试的CCK片段中,硫酸化的N端片段、CCK - 8序列的中间部分(CCK - 3 - 6片段)和C端四肽在尾部夹捏期间抑制大鼠的食物摄入,而C端三肽则显著增加食物摄入。结果表明,CCK肽根据给药途径通过不同机制抑制尾部夹捏诱导的摄食。