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酶促降解在新生大鼠脊髓速激肽神经递质失活中的作用。

Involvement of enzymatic degradation in the inactivation of tachykinin neurotransmitters in neonatal rat spinal cord.

作者信息

Suzuki H, Yoshioka K, Yanagisawa M, Urayama O, Kurihara T, Hosoki R, Saito K, Otsuka M

机构信息

Department of Pharmacology, Faculty of Medicine, Tokyo Medical and Dental University, Japan.

出版信息

Br J Pharmacol. 1994 Sep;113(1):310-6. doi: 10.1111/j.1476-5381.1994.tb16210.x.

Abstract
  1. The possible involvement of enzymatic degradation in the inactivation of tachykinin neurotransmitters was examined in the spinal cord of the neonatal rat. 2. The magnitude of substance P (SP)- or neurokinin A (NKA)-evoked depolarization of a lumbar ventral root in the isolated spinal cord preparation was increased by a mixture of peptidase inhibitors, consisting of actinonin (6 microM), arphamenine B (6 microM), bestatin (10 microM), captopril (10 microM) and thiorphan (0.3 microM). The mixture augmented the response to NKA more markedly than that to SP. 3. In the isolated spinal cord-cutaneous nerve preparation, the saphenous nerve-evoked slow depolarization of the L3 ventral root was augmented by the mixture of peptidase inhibitors in the presence of naloxone (0.5 microM) but not in the presence of both naloxone and a tachykinin receptor antagonist, GR71251 (5 microM). 4. Application of capsaicin (0.5 microM) for 6 min to the spinal cord evoked an increase in the release of SP from the spinal cord. The amount of SP released was significantly augmented by the mixture of peptidase inhibitors. 5. Synaptic membrane fractions were prepared from neonatal rat spinal cords. These fractions showed degrading activities for SP and NKA and the activities were inhibited by the mixture of peptidase inhibitors. The degrading activity for NKA was higher than that for SP and the inhibitory effect of the mixture for NKA was more marked than that for SP. Although some other fractions obtained from homogenates of spinal cords showed higher degrading activities for SP, these activities were insensitive to the mixture of peptidase inhibitors. 6. Effects of individual peptidase inhibitors on the enzymatic degradation of SP and NKA by synaptic membrane fractions were examined. Thiorphan, actinonin and captopril inhibited SP degradation, while thiorphan and actinonin, but not captopril, inhibited NKA degradation. The potency of the inhibition of each peptidase inhibitor was lower than that of the mixture.7. The present results suggest that enzymatic degradation is involved in the inactivation of tachykinin neurotransmitters in the spinal cord of the neonatal rat.
摘要
  1. 在新生大鼠脊髓中研究了酶促降解在速激肽神经递质失活过程中可能发挥的作用。2. 在离体脊髓制备物中,由抑肽酶(6微摩尔)、阿弗菌素B(6微摩尔)、贝司他汀(10微摩尔)、卡托普利(10微摩尔)和硫氧还蛋白(0.3微摩尔)组成的肽酶抑制剂混合物可增强P物质(SP)或神经激肽A(NKA)诱发的腰段腹根去极化幅度。该混合物对NKA反应的增强作用比对SP的更显著。3. 在离体脊髓 - 皮神经制备物中,在纳洛酮(0.5微摩尔)存在下,肽酶抑制剂混合物可增强隐神经诱发的L3腹根慢去极化,但在纳洛酮和速激肽受体拮抗剂GR71251(5微摩尔)同时存在时则不然。4. 向脊髓施加辣椒素(0.5微摩尔)6分钟可引起脊髓中SP释放增加。肽酶抑制剂混合物可显著增强SP的释放量。5. 从新生大鼠脊髓制备突触膜组分。这些组分对SP和NKA显示出降解活性,且该活性受到肽酶抑制剂混合物的抑制。对NKA的降解活性高于对SP的,混合物对NKA的抑制作用比对SP的更显著。尽管从脊髓匀浆中获得的其他一些组分对SP显示出更高的降解活性,但这些活性对肽酶抑制剂混合物不敏感。6. 研究了单个肽酶抑制剂对突触膜组分对SP和NKA酶促降解的影响。硫氧还蛋白、抑肽酶和卡托普利抑制SP降解,而硫氧还蛋白和抑肽酶而非卡托普利抑制NKA降解。每种肽酶抑制剂的抑制效力均低于混合物。7. 目前的结果表明,酶促降解参与了新生大鼠脊髓中速激肽神经递质的失活。

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