Osher Center for Integrative Medicine, Stockholm Brain Institute, Department of Clinical Neuroscience Karolinska Institutet, Stockholm, Sweden.
PLoS One. 2011 Mar 15;6(3):e17752. doi: 10.1371/journal.pone.0017752.
The main aim of this study was to assess if the perception of thermal pain thresholds is associated with genetically inferred levels of expression of the 5-HT transporter (5-HTT). Additionally, the perception of the so-called thermal grill illusion (TGI) was assessed. Forty-four healthy individuals (27 females, 17 males) were selected a-priori based on their 5-HTTLPR/rs25531 ('tri-allelic 5-HTTLPR') genotype, with inferred high or low 5-HTT expression. Thresholds for heat- and cold-pain were determined along with the sensory and affective dimensions of the TGI.
Thresholds to heat- and cold-pain correlated strongly (rho = -0.58, p<0.001). Individuals in the low 5-HTT-expressing group were significantly less sensitive to heat-pain (p = 0.02) and cold-pain (p = 0.03), compared to the high-expressing group. A significant gender-by-genotype interaction also emerged for cold-pain perception (p = 0.02); low 5-HTT-expressing females were less sensitive. The TGI was rated as significantly more unpleasant (affective-motivational dimension) than painful (sensory-discriminatory dimension), (p<0.001). Females in the low 5-HTT expressing group rated the TGI as significantly less unpleasant than high 5-HTT expressing females (p<0.05), with no such differences among men.
CONCLUSION/SIGNIFICANCE: We demonstrate an association between inferred low 5-HTT expression and elevated thresholds to thermal pain in healthy non-depressed individuals. Despite the fact that reduced 5-HTT expression is a risk factor for chronic pain we found it to be related to hypoalgesia for threshold thermal pain. Low 5-HTT expression is, however, also a risk factor for depression where thermal insensitivity is often seen. Our results may thus contribute to a better understanding of the molecular underpinnings of such paradoxical hypoalgesia. The results point to a differential regulation of thermoafferent-information along the neuraxis on the basis of 5-HTT expression and gender. The TGI, suggested to rely on the central integration of thermoafferent-information, may prove a valuable tool in probing the affective-motivational dimension of these putative mechanisms.
本研究的主要目的是评估热痛觉阈值的感知是否与 5-羟色胺转运体(5-HTT)的基因推断表达水平相关。此外,还评估了所谓的热格栅错觉(TGI)的感知。根据其 5-HTTLPR/rs25531(“三等位基因 5-HTTLPR”)基因型,预先选择了 44 名健康个体(27 名女性,17 名男性),具有高或低 5-HTT 表达的推断。确定了热痛觉和冷痛觉的阈值,以及 TGI 的感觉和情感维度。
热痛觉和冷痛觉阈值之间存在很强的相关性(rho=-0.58,p<0.001)。与高表达组相比,低 5-HTT 表达组对热痛觉(p=0.02)和冷痛觉(p=0.03)的敏感性显著降低。对于冷痛觉感知,还出现了显著的性别-基因型相互作用(p=0.02);低 5-HTT 表达的女性敏感性较低。TGI 的评分明显比疼痛(感觉区分维度)更不愉快(情感动机维度)(p<0.001)。低 5-HTT 表达组的女性对 TGI 的评分明显低于高 5-HTT 表达的女性(p<0.05),而男性之间没有差异。
结论/意义:我们证明了在健康非抑郁个体中,推断的低 5-HTT 表达与热痛觉阈值升高之间存在关联。尽管降低 5-HTT 表达是慢性疼痛的危险因素,但我们发现它与阈值热痛觉的低痛觉有关。然而,低 5-HTT 表达也是抑郁的危险因素,其中通常会出现热不敏感。我们的结果可能有助于更好地理解这种矛盾性低痛觉的分子基础。结果表明,基于 5-HTT 表达和性别,沿轴突对热感觉信息进行了差异调节。TGI 被认为依赖于热感觉信息的中枢整合,可能是探测这些假定机制的情感动机维度的有效工具。