Endocrine Unit of First Department of Internal Medicine, Faculty of Medicine, University of Szeged, Korányi fasor 8-10, H-6720, Szeged, Hungary.
Physiol Behav. 2011 Jul 6;103(5):421-30. doi: 10.1016/j.physbeh.2011.03.016. Epub 2011 Mar 16.
Many chemicals utilized by humans are present as environmental pollutants and may influence homeostasis from neurological, immunological, endocrinological and/or behavioral aspects. Such agents, acting alone or in ambient mixtures, may be biologically active even at extremely low doses, and it may be postulated that stable, bioaccumulative, reactive endocrine disruptors may affect central and/or peripheral secretion of arginine-vasopressin (AVP) and oxytocin (OXT) and thereby related physiological and behavioral functions, potentially leading to disorders in exposed subjects. The primary aim of this study was to demonstrate effects of chronic exposure to a low dose of an orally administered chlorobenzene mixture on anxiety-related and aggressive behavior mediated largely by AVP and OXT. Chlorobenzenes were applied to model ambient mixtures of endocrine disruptors. Adult, male Wistar rats were exposed daily to 0.1 μg/kg of 1,2,4-trichlorobenzene and hexachlorobenzene via a stomach tube for 30, 60 or 90 days, after which anxiety-related and aggressive behavioral elements were examined in open-field, elevated plus maze and resident-intruder tests. The plasma levels of AVP, OXT and adrenocorticotrophic hormone at the endpoints were measured by radioimmunoassay or immunochemiluminescence assay. The levels of basal and serotonin- or norepinephrine-stimulated AVP and OXT secretion in pituicyte cultures prepared from the posterior lobe of the pituitaries were also measured. The hormone levels proved to be increased to extents depending on the duration of exposure to the chlorobenzenes. Several anxiety-related and aggressive behavioral elements were also enhanced following chlorobenzene exposure, while certain explorative and locomotive elements of the animals were decreased. As both physiological and behavioral elements were modulated by chronic, subtoxic doses of chlorobenzenes, it is concluded that doses of such environmental pollutants low enough to fall outside the range of legal regulation may pose potential risks of anxiogenic and/or aggressive consequences in exposed subjects, including humans.
许多人类使用的化学物质作为环境污染物存在,可能会从神经、免疫、内分泌和/或行为方面影响体内平衡。这些单独或在环境混合物中存在的物质,即使在极低剂量下也可能具有生物活性,并且可以假设稳定、生物累积、反应性的内分泌干扰物可能会影响精氨酸加压素(AVP)和催产素(OXT)的中枢和/或外周分泌,并由此影响相关的生理和行为功能,从而导致暴露人群出现疾病。本研究的主要目的是证明慢性低剂量口服摄入氯苯混合物对焦虑相关和攻击性行为的影响,这些行为主要由 AVP 和 OXT 介导。氯苯被用于模拟内分泌干扰物的环境混合物。成年雄性 Wistar 大鼠通过胃管每天接受 0.1μg/kg 的 1,2,4-三氯苯和六氯苯,连续 30、60 或 90 天,然后在开放场、高架十字迷宫和群居-入侵试验中检查焦虑相关和攻击性行为成分。通过放射免疫或免疫化学发光测定在终点测量 AVP、OXT 和促肾上腺皮质激素的血浆水平。还测量了从垂体后叶制备的垂体细胞培养物中基础和 5-羟色胺或去甲肾上腺素刺激的 AVP 和 OXT 分泌水平。激素水平的增加程度取决于暴露于氯苯的时间长短。在氯苯暴露后,几种与焦虑相关和攻击性行为成分也得到增强,而动物的某些探索和运动成分则减少。由于生理和行为成分均受到慢性、亚毒性剂量的氯苯调节,因此可以得出结论,此类环境污染物的剂量低到足以超出法律规定的范围,可能会对暴露人群(包括人类)产生焦虑和/或攻击性后果的潜在风险。