Effect of haloperidol on the numeric density of neurons and nuclear height in the rat hippocampus: A stereological and histopathological study

B. Unal, M. Özbek, Aydin, N. Aydın, Z. Bulucu, Ozgen Vuraler, E. Odacı, B. Sahin, S. Kaplan
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引用次数: 24

Abstract

In recent studies, some neuroleptics have shown neurotoxic activities. Clinical and experimental studies have been carried out to investigate the effects of different neuroleptic drugs considered to affect the central nervous system. The aim of this study was to evaluate neurotoxic effects of halperidol on hippocampal neurons. The drug was given in daily doses of either 1 or 3 mg/kg for 6 weeks to adult male guinea pigs. After treatment, all animals were anaesthetized via short inhalation of ether, and then were fixed by a mixture of 2% glutaraldehyde and +2% paraformaldehyde in 0.1 M phosphate buffer. Brains were removed from the cranium and stored in the same fixative overnight. On the following day, the CA1 region of the hippocampus was dissected out. After embedding in araldite resin and obtaining semi-thin sections, the tissues were stained with toluidine blue. The physical dissector was used for measurements of nuclear height and numerical density of neurons and the sections were also evaluated histopathologically. The numerical density of neurons and nuclear height in the hippocampus for the low-dose (1 mg/kg) and high-dose (3 mg/kg) experimental groups were 12.4 mm3 and 3.6 μm and 7.14 mm3 and 3.56 μm, respectively. In contrast, the control group had a neuronal numerical density of 16.55 mm −3 and a nuclear height of 4.09 μm. There was a significant difference in both the mean density of neurons and the mean height of nuclei between haloperidol-treated and control groups (p < 0.05). There was also a statistical difference in the mean density of neurons (but not in nuclear height) when comparing the dosage of haloperidol (p < 0.05). These findings suggest that haloperidol treatment may lead to a loss of neurons as well as a decrease in the height of nuclei in the hippocampus.
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氟哌啶醇对大鼠海马神经元数量密度和核高度的影响:一项体视学和组织病理学研究
在最近的研究中,一些抗精神病药显示出神经毒性。已经进行了临床和实验研究,以调查被认为影响中枢神经系统的不同抗精神病药物的作用。本研究的目的是评估氟哌啶醇对海马神经元的神经毒性作用。给成年雄性豚鼠每日1或3 mg/kg剂量,连续6周。治疗后,所有动物短时间吸入乙醚麻醉,然后用0.1% M磷酸盐缓冲液中2%戊二醛和+2%多聚甲醛的混合物固定。大脑从头盖骨中取出,在相同的固定液中保存过夜。第二天,切除海马CA1区。将组织包埋于钠盐树脂中,获得半薄切片,用甲苯胺蓝染色。物理解剖仪用于测量核高度和神经元的数值密度,并对切片进行组织病理学评估。低剂量组(1 mg/kg)和高剂量组(3 mg/kg)海马神经元数量密度和核高度分别为12.4 mm3和3.6 μm, 7.14 mm3和3.56 μm。对照组神经元数值密度为16.55 mm−3,核高度为4.09 μm。氟哌啶醇处理组与对照组神经元平均密度、核平均高度差异有统计学意义(p < 0.05)。氟哌啶醇给药组神经元平均密度差异有统计学意义(p < 0.05),核高度差异无统计学意义(p < 0.05)。这些发现表明氟哌啶醇治疗可能导致神经元的丧失以及海马核高度的降低。
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