Chelikani Prasanth K, Haver Alvin C, Reidelberger Roger D
Veterans Affairs-Nebraska Western Iowa Health Care System, Omaha, NE 68105, USA.
Am J Physiol Regul Integr Comp Physiol. 2004 Nov;287(5):R1064-70. doi: 10.1152/ajpregu.00376.2004. Epub 2004 Jul 8.
We compared the effects of the two molecular forms of the brain-gut peptide YY (PYY), PYY(1-36) and PYY(3-36), on gastric emptying. Unanesthetized rats received 20-min intravenous infusions of rat PYY(1-36) (0, 1.7, 5, 17, 50, 100, 170 pmol x kg(-1) x min(-1)) and rat PYY(3-36) (0, 0.5, 1.7, 5, 17, 50, 100, 170 pmol x kg(-1) x min(-1)), either alone or combined, and gastric emptying of saline was measured during the last 10 min of infusion. For comparison, human PYY(3-36) was administered at 0, 17, and 50 pmol x kg(-1) x min(-1). Gastric emptying was decreased by 11, 24, 26 and 38% in response to 17, 50, 100, and 170 pmol x kg(-1) x min(-1) of rat PYY(1-36); by 10, 26, 41, 53, and 57% in response to 5, 17, 50, 100, and 170 pmol x kg(-1) x min(-1) of rat PYY(3-36); and by 35 and 53% in response to 17 and 50 pmol x kg(-1) x min(-1) of human PYY(3-36), respectively. Estimated ED50s were 470 and 37 pmol x kg(-1) x min(-1) for rat PYY(1-36) and PYY(3-36), respectively. In general, within an experiment, coadministration of PYY(1-36) and PYY(3-36) inhibited gastric emptying by an amount that was comparable to that produced when either peptide was given alone. We conclude that 1) intravenous infusion of PYY(1-36) and PYY(3-36) each produces a dose-dependent inhibition of gastric emptying in rats, 2) PYY(3-36) is an order of magnitude more potent than PYY(1-36) in inhibiting gastric emptying, 3) human PYY(3-36) and rat PYY(3-36) inhibit gastric emptying similarly, and 4) PYY(1-36) and PYY(3-36) do not appear to interact in an additive or synergistic manner to inhibit gastric emptying.
我们比较了脑肠肽YY(PYY)的两种分子形式,即PYY(1 - 36)和PYY(3 - 36)对胃排空的影响。未麻醉的大鼠接受20分钟的大鼠PYY(1 - 36)(0、1.7、5、17、50、100、170 pmol·kg⁻¹·min⁻¹)和大鼠PYY(3 - 36)(0、0.5、1.7、5、17、50、100、170 pmol·kg⁻¹·min⁻¹)静脉输注,单独或联合输注,在输注的最后10分钟测量生理盐水的胃排空情况。为作比较,给予人PYY(3 - 36),剂量为0、17和50 pmol·kg⁻¹·min⁻¹。分别给予17、50、100和170 pmol·kg⁻¹·min⁻¹的大鼠PYY(1 - 36)后,胃排空分别降低11%、24%、26%和38%;分别给予5、17、50、100和170 pmol·kg⁻¹·min⁻¹的大鼠PYY(3 - 36)后,胃排空分别降低10%、26%、41%、53%和57%;分别给予17和50 pmol·kg⁻¹·min⁻¹的人PYY(3 - 36)后,胃排空分别降低35%和53%。大鼠PYY(1 - 36)和PYY(3 - 36)的估计半数有效剂量(ED50)分别为470和37 pmol·kg⁻¹·min⁻¹。一般来说,在一个实验中,联合给予PYY(1 - 36)和PYY(3 - 36)对胃排空的抑制程度与单独给予任何一种肽时相当。我们得出以下结论:1)静脉输注PYY(1 - 36)和PYY(3 - 36)均可在大鼠中产生剂量依赖性的胃排空抑制作用;2)在抑制胃排空方面,PYY(3 - 36)的效力比PYY(1 - 36)高一个数量级;3)人PYY(3 - 36)和大鼠PYY(3 - 36)对胃排空的抑制作用相似;4)PYY(1 - 36)和PYY(3 - 36)在抑制胃排空方面似乎不存在相加或协同作用。