Alteration of central serotonin modifies onset and severity of adjuvant-induced arthritis in the rat.

M S Harbuz, O Marti, S L Lightman, D S Jessop
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引用次数: 27

Abstract

Objective: Previous studies have determined that depletion of serotonin reduces the severity of hind-paw inflammation in adjuvant-induced arthritis (AA) in the rat. We wished to (i) test the hypothesis that this effect may be mediated, at least in part, through a central mechanism and (ii) to investigate further the pro-inflammatory role of serotonin we determined whether increasing serotonin using a selective serotonin reuptake inhibitor (SSRI), to increase serotonin availability at the active site of release, would increase inflammation.

Methods: (i) Serotonin was depleted in the brain of rats with the selective neurotoxin 5'7'-dihydroxytryptamine. (ii) Rats were treated with an SSRI on days 10, 11 and 12 following adjuvant injection. Hind-paw inflammation was determined with plethysmometry as an index of severity of inflammation, and brain, pituitaries and blood were collected for assessment of changes in the hypothalamo -pituitary adrenal (HPA) axis.

Results: (i) Serotonin depletion significantly reduced hind-paw inflammation. (ii) SSRI-treated animals developed hind-paw inflammation sooner, and the severity was increased compared to vehicle-treated AA rats. The changes in the HPA axis associated with inflammation were partly reversed by this treatment.

Conclusion: These data suggest a pro-inflammatory role for central serotonin in this disease model and indicate that treatment with SSRIs may exacerbate the development of inflammation.

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中枢血清素的改变改变了大鼠佐剂性关节炎的发病和严重程度。
目的:先前的研究已经确定,血清素的消耗可以降低大鼠佐剂性关节炎(AA)中后爪炎症的严重程度。我们希望(i)检验这种效应可能是通过一个中心机制介导的假设,至少在一定程度上是这样;(ii)为了进一步研究血清素的促炎作用,我们确定了使用选择性血清素再摄取抑制剂(SSRI)来增加血清素,以增加活性部位释放的血清素可用性,是否会增加炎症。方法:(1)用选择性神经毒素5′7′-二羟色胺使大鼠脑内血清素减少。(ii)大鼠在佐剂注射后第10、11、12天给予SSRI治疗。用胸腺体积测量法测定后爪炎症程度,并采集脑、垂体和血液,评估下丘脑-垂体肾上腺(HPA)轴的变化。结果:(1)血清素缺失显著减轻后爪炎症。(ii) ssri处理的大鼠后爪炎症发生得更快,且严重程度较药液处理的AA大鼠有所增加。这种治疗部分逆转了与炎症相关的下丘脑轴的变化。结论:这些数据表明中枢5 -羟色胺在该疾病模型中具有促炎作用,并表明SSRIs治疗可能加剧炎症的发展。
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