Casares Federico M, McElroy Anne, Mantione Kirk, Baggermann Geert, Zhu Wei, Stefano George B
Neuroscience Research Institute, State University of New York, College at Old Westbury, Old Westbury, NY 11568, USA.
Neuro Endocrinol Lett. 2005 Apr;26(2):89-97.
The study was designed to determine if morphine was present in lobster tissues. It was also important to determine, as in other animals, if its levels would change in response to stress. In this regard, it was also important to determine if lobster immune and neural tissues express the mu opiate receptor subtype, which was coupled to constitutive nitric oxide synthase derived nitric oxide release.
Homarus americanus were used in these experiments. Morphine was purified in lobster tissues via high pressure liquid chromatography coupled to UV detection. It was quantified via radioimmunoassay (RIA) and was identified via quadruple time of flight - mass spectrometry. Animals were subject to 2 forms of trauma, namely pereiopod-ablation or lipopolysaccaride (LPS) - injection, and morphine levels determined in nerve cord or hemolymph. Real-time nitric oxide production was determined via an amperometric probe. RT-PCR was used to determine the presence of a micro opiate receptor transcript.
In Homarus americanus hemolymph and nerve cord morphine was found. RIA revealed morphine levels of 3.36 pg/mg +/ - 0.48 SEM (N=8) in nerve cord and 717.88 pg/ml +/ - 56.77 SEM (N=58) in hemolymph. In stressed (pereiopod-ablated or LPS-injected) animals, the endogenous morphine levels initially increased significantly by 24% for hemolymph and 48% for nerve cord. By day 5, the stressed and control values for endogenous morphine, in both tissues, was lower and non-distinguishable. In both hemocytes and neural cells, morphine, not met-enkephalin, stimulated constitutive nitric oxide release in a naloxone antagonizable manner, demonstrating a mu opiate receptor mediated phenomenon and suggesting the presence of the mu opiate receptor subtype, micro3, since it is opiate alkaloid selective and opioid peptide insensitive. RT-PCR revealed the presence of a micro opiate receptor transcript in Homarus neural and immune tissues, which exhibits a 100% sequence identity with its human counterpart.
Taken together, after eliminating all sources of contamination, morphine is present in lobster tissues, potentially demonstrating hormonal and neurotransmitter functions that are involved in the animals' stress response.
本研究旨在确定龙虾组织中是否存在吗啡。与其他动物一样,确定其水平是否会因应激而变化也很重要。在这方面,确定龙虾免疫和神经组织是否表达μ阿片受体亚型也很重要,该亚型与组成型一氧化氮合酶衍生的一氧化氮释放相关。
本实验使用美洲螯龙虾。通过与紫外检测联用的高压液相色谱法在龙虾组织中纯化吗啡。通过放射免疫测定法(RIA)对其进行定量,并通过四极杆飞行时间质谱法进行鉴定。对动物施加两种形式的创伤,即步足切除或脂多糖(LPS)注射,并测定神经索或血淋巴中的吗啡水平。通过安培探针测定实时一氧化氮产量。使用逆转录聚合酶链反应(RT-PCR)确定微阿片受体转录本的存在。
在美洲螯龙虾的血淋巴和神经索中发现了吗啡。RIA显示神经索中的吗啡水平为3.36 pg/mg ± 0.48 SEM(N = 8),血淋巴中的吗啡水平为717.88 pg/ml ± 56.77 SEM(N = 58)。在应激(步足切除或注射LPS)的动物中,血淋巴中内源性吗啡水平最初显著增加24%,神经索中增加48%。到第5天,两种组织中应激组和对照组的内源性吗啡值均较低且无差异。在血细胞和神经细胞中,吗啡而非甲硫氨酸脑啡肽以纳洛酮可拮抗的方式刺激组成型一氧化氮释放,表明这是一种μ阿片受体介导的现象,并提示存在μ阿片受体亚型μ3,因为它对阿片生物碱具有选择性且对阿片肽不敏感。RT-PCR显示在美洲螯龙虾的神经和免疫组织中存在微阿片受体转录本,其与人类对应物具有100%的序列同一性。
综上所述,在消除所有污染来源后,龙虾组织中存在吗啡,这可能表明其具有参与动物应激反应的激素和神经递质功能。