Orchard I, Loughton B G
J Neurobiol. 1981 Mar;12(2):143-53. doi: 10.1002/neu.480120204.
The release of hyperlipemic hormone from the glandular cells of the corpus cardiacum (CC) of Locusta migratoria is under the synaptic control of axons in nervus corpus cardiacum II (NCC II). The effects of aminergic agonists and antagonists on the release of the hyperlipemic hormone induced by electrical stimulation of NCC II have been examined. CC isolated from reserpine-injected locusts did not release hormone when subjected to electrical stimulation of NCC II but continued to release hormone in response to high-potassium saline. The electrically stimulated release of hormone from isolated CC was abolished by the alpha-adrenergic blocking agent, phenoxybenzamine, but potentiated by the beta-adrenergic blocking agent, propranolol. Phenoxybenzamine did not interfere with release induced by high-potassium saline. It is suggested that the postsynaptic receptors on the glandular cells are similar to the alpha-adrenergic receptors of vertebrates. Octopamine was found to be present in the glandular lobe of the CC at concentrations of 0.62 pmole per gland pair. Reserpine depleted the content to 0.3 pmole per pair. Bathing the CC in 10(-7) M octopamine resulted in the release of hyperlipemic hormone, and this release was blocked by phenoxybenzamine. It is concluded that the neurotransmitter involved in the synapse between axons of NCC II and the cells releasing hyperlipemic hormone is aminergic, possibly octopaminergic. Octopamine may well be a transmitter mediating hormone release in insects.
飞蝗心侧体腺细胞中促脂激素的释放受心侧体神经II(NCC II)轴突的突触控制。已研究了胺能激动剂和拮抗剂对电刺激NCC II诱导的促脂激素释放的影响。从注射利血平的飞蝗分离得到的心侧体,在受到NCC II的电刺激时不释放激素,但对高钾盐水仍能继续释放激素。α-肾上腺素能阻断剂酚苄明可消除分离的心侧体经电刺激后的激素释放,但β-肾上腺素能阻断剂普萘洛尔可增强这种释放。酚苄明不干扰高钾盐水诱导的释放。这表明腺细胞上的突触后受体与脊椎动物的α-肾上腺素能受体相似。发现章鱼胺在心侧体腺叶中的浓度为每对腺体0.62皮摩尔。利血平使含量降至每对0.3皮摩尔。将心侧体置于10^(-7) M章鱼胺中孵育会导致促脂激素释放,且这种释放被酚苄明阻断。得出的结论是,NCC II轴突与释放促脂激素的细胞之间突触所涉及的神经递质是胺能的,可能是章鱼胺能的。章鱼胺很可能是介导昆虫激素释放的一种递质。