Heilig M, Ekman R
Department of Clinical Neuroscience, Göteborg University, Mölndal Hospital, Sweden.
Neurochem Int. 1995 Apr;26(4):351-5. doi: 10.1016/0197-0186(94)00150-s.
We have previously reported elevated brain tissue contents of neuropeptide Y-like immunoreactivity (NPY-LI) following 3 weeks of oral treatment with the antidepressants zimelidine and imipramine. Other studies have not reproduced this finding. To eliminate the possibility that this has been due to insufficient treatment duration, dosage, or differences in route of administration or assay specificity, we have administered the selective serotonin reuptake inhibitor citalopram and the preferential noradrenaline reuptake inhibitor desmethylimipramine parenterally for 6 weeks. NPY-LI was assayed using both the assay employed in the original study, and an assay based on a different antiserum which has been extensively examined for cross-reactivity. To exclude the possibility that differential processing rather than altered synthesis rate is responsible for apparent changes in NPY-LI, HPLC analysis of immunoreactive fragment profiles was used. No differences in NPY-LI levels were seen in the brain regions examined, and no differences in HPLC profiles of NPY-LI were present with either drug. We conclude that chronic parenteral administration of antidepressant drugs in naïve (non-depressed) animals does not affect the synthesis or processing of NPY. Another neuropeptide implicated in mechanisms of depression, corticotropin-releasing hormone (CRH) was also found to be unaffected by a similar analysis.
我们之前曾报道,在用抗抑郁药齐美利定和丙咪嗪进行3周口服治疗后,脑组织中神经肽Y样免疫反应性(NPY-LI)含量升高。其他研究并未重现这一发现。为了排除这是由于治疗持续时间不足、剂量、给药途径或检测特异性差异所致的可能性,我们对选择性5-羟色胺再摄取抑制剂西酞普兰和优先去甲肾上腺素再摄取抑制剂去甲丙咪嗪进行了为期6周的非肠道给药。使用原始研究中采用的检测方法以及基于另一种已对交叉反应性进行广泛检测的抗血清的检测方法对NPY-LI进行检测。为了排除是差异加工而非合成速率改变导致NPY-LI出现明显变化的可能性,我们使用高效液相色谱法(HPLC)分析了免疫反应性片段图谱。在所检测的脑区中未发现NPY-LI水平存在差异,且两种药物的NPY-LI的HPLC图谱均未出现差异。我们得出结论,在未经治疗(非抑郁)的动物中,长期非肠道给予抗抑郁药物不会影响NPY的合成或加工。另一种与抑郁机制有关的神经肽促肾上腺皮质激素释放激素(CRH),经类似分析也发现未受影响。