Haleem Darakhshan Jabeen
Department of Biochemistry, Neurochemistry and Biochemical Neuropharmacology Research Unit, University of Karachi, Karachi 75270, Pakistan.
Appetite. 2009 Feb;52(1):44-50. doi: 10.1016/j.appet.2008.07.009. Epub 2008 Aug 5.
5-Hydroxytryptamine (5-HT; serotonin) system is the major neurotransmitter system of interest in research on anorexia nervosa (AN). The AN patients show extreme dieting weight loss, hyperactivity and low basal levels of 5-hydroxyindoleacetic acid (5-HIAA), a major metabolite of 5-HT in the cerebrospinal fluid (CSF). Studies on animal models show that diet restriction (DR) decreases 5-HT metabolism in the brain and hypothalamus which is not necessarily associated with a decrease in the availability of essential amino acid tryptophan (TRP) the precursor of serotonin. To further investigate the mechanism involved in DR-induced decreases of 5-HT the present study uses 8-hydroxy-(2-di-n-propylamino) tetralin (8-OH-DPAT), a selective 5-HT-1A agonist, as a probe to monitor the responsiveness of negative feedback control over 5-HT metabolism. Effects of DR and of 8-OHDPAT on TRP, 5-HT and 5-HIAA concentrations are determined in the hypothalamus, a region of the brain known to role in the regulation of appetite. Animals of DR group given access to food 2h daily for 6 days exhibited 21.6% decrease in the body weight compared to freely feeding (FF) controls. The levels of TRP in the plasma and of 5-HT in the hypothalamus decreased. No effect was found on the levels of TRP in the hypothalamus. 8-OH-DPAT-induced decreases of 5-HT and 5-HIAA were greater in DR than FF group. 8-OH-DPAT-induced hyperactivity was also greater in DR than FF group. The results show that DR-induced decreases of 5-HT are due to an increase in the responsiveness of negative feedback control over 5-HT and not due to smaller availability of TRP. DR-induced increase in activity and 8-OH-DPAT-induced greater hyperactivity in DR than FF group may also be due to exaggerated negative feedback control over 5-HT. It is suggested that drugs decreasing the responsiveness of negative feedback control over 5-HT may be of use for the treatment and prevention of AN in under weight patients on restricted diet.
5-羟色胺(5-HT;血清素)系统是神经性厌食症(AN)研究中主要关注的神经递质系统。AN患者表现出极端节食导致体重减轻、多动,且脑脊液(CSF)中5-羟色胺的主要代谢产物5-羟吲哚乙酸(5-HIAA)的基础水平较低。对动物模型的研究表明,饮食限制(DR)会降低大脑和下丘脑的5-HT代谢,而这不一定与血清素前体必需氨基酸色氨酸(TRP)的可用性降低有关。为了进一步研究DR诱导的5-HT降低所涉及的机制,本研究使用选择性5-HT-1A激动剂8-羟基-(2-二正丙基氨基)四氢萘(8-OH-DPAT)作为探针,来监测对5-HT代谢的负反馈控制的反应性。在已知对食欲调节起作用的大脑区域下丘脑,测定DR和8-OH-DPAT对TRP、5-HT和5-HIAA浓度的影响。与自由进食(FF)对照组相比,DR组动物每天进食2小时,持续6天,体重下降了21.6%。血浆中TRP水平和下丘脑中5-HT水平降低。未发现对下丘脑中TRP水平有影响。DR组中8-OH-DPAT诱导的5-HT和5-HIAA降低比FF组更大。DR组中8-OH-DPAT诱导的多动也比FF组更大。结果表明,DR诱导的5-HT降低是由于对5-HT的负反馈控制反应性增加,而不是由于TRP可用性降低。DR诱导的活动增加以及DR组中8-OH-DPAT诱导的比FF组更大的多动也可能是由于对5-HT的负反馈控制过度。建议降低对5-HT负反馈控制反应性的药物可能对治疗和预防节食的体重过轻患者的AN有用。