Moscow Medical Dental University, Moscow, Russia.
Med Sci Monit. 2009 Oct;15(10):BR289-292.
Human dental pulp contains monoamine oxidase (MAO) and semicarbazide sensitive amine oxidase (SSAO). In other tissues SSAO is involved in oxidative stress and inflammation, but the role of MAO and SSAO in human pulp and changes of their activities in reversible pulpitis still remains poorly understood.
MATERIAL/METHODS: We investigated MAO labeling with mechanism-based inhibitor [3H]pargyline activities of MAO A, MAO B, and SSAO in healthy and inflamed human dental pulp.
Incubation of human dental pulp homogenates with [3H]pargyline caused MAO labeling. MAO activity assayed with 100 microM [14C]5HT or 10 microM [14C]PEA was sensitive to selective inhibitors of MAO A and MAO B, respectively. MAO activity with 50 microM [14C]PEA was partially inhibited by clorgyline, and total inhibition was achieved only by the combination of clorgyline and semicarbazide, suggesting the presence of SSAO. Inflammation of the dental pulp was accompanied by a significant decrease in MAO labeling, MAO B (but not MAO A) activity and the increase in SSAO activity.
The results of the present study suggest that the increase of dental pulp SSAO activity contributes to the development of inflammation in the dental pulp. The decrease in MAO B activity and lack of significant changes in MAO A activity may be associated with an anti-inflammatory response - inflamed pulp MAO A still effectively deaminates the inflammatory mediator 5HT, whereas inhibition of MAO B could result in some decrease of hydrogen peroxide generation, essential for the tissue damage in inflammation.
人类牙髓中含有单胺氧化酶(MAO)和脒基化敏感胺氧化酶(SSAO)。在其他组织中,SSAO 参与氧化应激和炎症,但 MAO 和 SSAO 在人牙髓中的作用及其在可逆性牙髓炎中的活性变化仍知之甚少。
材料/方法:我们研究了用基于机制的抑制剂[3H]帕吉林对 MAO A、MAO B 和 SSAO 的 MAO 标记活性,以及健康和发炎的人牙髓。
人牙髓匀浆与[3H]帕吉林孵育可引起 MAO 标记。用 100μM[14C]5-HT 或 10μM[14C]PEA 测定 MAO 活性,对 MAO A 和 MAO B 的选择性抑制剂均敏感。用 50μM[14C]PEA 测定 MAO 活性,被氯丙嗪部分抑制,仅氯丙嗪和脒基化联合完全抑制,提示存在 SSAO。牙髓炎症伴随着 MAO 标记、MAO B(而非 MAO A)活性的显著下降和 SSAO 活性的增加。
本研究结果表明,牙髓 SSAO 活性的增加有助于牙髓炎症的发展。MAO B 活性的下降和 MAO A 活性的无显著变化可能与抗炎反应有关——炎症牙髓中的 MAO A 仍能有效地脱氨基炎症介质 5-HT,而 MAO B 的抑制可能导致过氧化氢生成的一些减少,这对炎症中的组织损伤至关重要。