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分泌蛋白Bv8引起的伤害性感受敏化

Nociceptive sensitization by the secretory protein Bv8.

作者信息

Negri Lucia, Lattanzi Roberta, Giannini Elisa, Metere Alessio, Colucci Mariantonella, Barra Donatella, Kreil Günther, Melchiorri Pietro

机构信息

Department of Human Physiology and Pharmacology V. Erspamer, University La Sapienza, 00185 Rome, Italy.

出版信息

Br J Pharmacol. 2002 Dec;137(8):1147-54. doi: 10.1038/sj.bjp.0704995.

DOI:10.1038/sj.bjp.0704995
PMID:12466223
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1573618/
Abstract

1 The small protein Bv8, isolated from amphibian skin, belongs to a novel family of secretory proteins (Bv8-Prokineticin family, SWISS-PROT: Q9PW66) whose orthologues have been conserved throughout evolution, from invertebrates to humans. 2 When injected intravenously or subcutaneously (from 0.06 to 500 pmol kg(-1)) or intrathecally (from 6 fmol to 250 pmol) in rats, Bv8 produced an intense systemic nociceptive sensitization to mechanical and thermal stimuli applied to the tail and paws. 3 Topically delivered into one rat paw, 50 fmol of Bv8 decreased by 50% the nociceptive threshold to pressure in the injected paw without affecting the threshold in the contralateral paw. 4 The two G-protein coupled prokineticin receptors, PK-R1 and PK-R2, were expressed in rat dorsal root ganglia (DRG) and in dorsal quadrants of spinal cord (DSC) and bound Bv8 and the mammalian orthologue, EG-VEGF, with high affinity. In DSC, PK-R1 was more abundant than PK-R2, whereas both receptors were equally expressed in DRG. IC(50) of Bv8 and EG-VEGF to inhibit [(125)I]-Bv8 binding to rat DRG and DSC were 4.1+/-0.4 nM Bv8 and 76.4+/-7.6 nM EG-VEGF, in DRG; 7.3+/-0.9 nM Bv8 and 330+/-41 nM EG-VEGF, in DSC. 5 In the small diameter neurons (<30 microm) of rat DRG cultures, Bv8 concentrations, ranging from 0.2 to 10 nM, raised Ca(2+) in a dose-dependent manner. 6 These data suggest that Bv8, through binding to PK receptors of DSC and primary sensitive neurons, results in intense sensitization of peripheral nociceptors to thermal and mechanical stimuli.

摘要
  1. 从小型两栖动物皮肤中分离出的小蛋白Bv8,属于一个新的分泌蛋白家族(Bv8-促动力蛋白家族,SWISS-PROT:Q9PW66),其直系同源物在从无脊椎动物到人类的整个进化过程中都得到了保留。2. 当以静脉内或皮下注射(0.06至500 pmol kg(-1))或鞘内注射(6 fmol至250 pmol)的方式给予大鼠时,Bv8会对施加于尾巴和爪子的机械和热刺激产生强烈的全身性伤害性敏感化。3. 将50 fmol的Bv8局部施用于一只大鼠的爪子,可使注射爪子对压力的伤害性阈值降低50%,而不影响对侧爪子的阈值。4. 两种G蛋白偶联的促动力蛋白受体PK-R1和PK-R2在大鼠背根神经节(DRG)和脊髓背侧象限(DSC)中表达,并以高亲和力结合Bv8和哺乳动物直系同源物EG-VEGF。在DSC中,PK-R1比PK-R2丰富,而在DRG中两种受体表达量相等。Bv8和EG-VEGF抑制[(125)I]-Bv8与大鼠DRG和DSC结合的IC(50),在DRG中分别为4.1±0.4 nM Bv8和76.4±7.6 nM EG-VEGF;在DSC中分别为7.3±0.9 nM Bv8和330±41 nM EG-VEGF。5. 在大鼠DRG培养物的小直径神经元(<30微米)中,0.2至10 nM范围内的Bv8浓度以剂量依赖性方式升高Ca(2+)。6. 这些数据表明,Bv8通过与DSC和初级感觉神经元的PK受体结合,导致外周伤害感受器对热和机械刺激产生强烈的敏感化。

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