Park J H, Keeley L L
Department of Entomology, Texas A&M University, College Station, Texas, 77843, USA.
Gen Comp Endocrinol. 1998 Apr;110(1):88-95. doi: 10.1006/gcen.1997.7053.
Several biogenic amines and their analogs were examined for stimulatory effects on glycogen phosphorylase activity and trehalose biosynthesis in fat body of the cockroach, Blaberus discoidalis. Octopamine and synephrine were the most potent activators of fat body phosphorylase; 10 muM octopamine being nearly as effective as the hypertrehalosemic hormone (HTH). Epinephrine, norepinephrine, and tyramine produced intermediate effects, whereas dopamine, 5-hydroxytryptamine, and melatonin had no effect. The fat body octopamine receptors appeared to be pharmacologically related to vertebrate alpha-adrenergic receptors and belonged to the Octopamine1 class receptor. In contrast to previous reports, synephrine also induced both phosphorylase activation and hypertrehalosemia as effectively as octopamine. Demethylchlordimeform, a formamidine insecticide structurally similar to octopamine, also strongly activated fat body phosphorylase, possibly by interaction with the octopamine receptor.
研究了几种生物胺及其类似物对蜚蠊(Blaberus discoidalis)脂肪体中糖原磷酸化酶活性和海藻糖生物合成的刺激作用。章鱼胺和辛弗林是脂肪体磷酸化酶最有效的激活剂;10μM章鱼胺的效果几乎与高海藻糖血症激素(HTH)相同。肾上腺素、去甲肾上腺素和酪胺产生中等效果,而多巴胺、5-羟色胺和褪黑素则没有效果。脂肪体章鱼胺受体在药理学上似乎与脊椎动物α-肾上腺素能受体相关,属于章鱼胺1类受体。与先前的报道相反,辛弗林也能像章鱼胺一样有效地诱导磷酸化酶激活和高海藻糖血症。脱甲基杀虫脒是一种结构与章鱼胺相似的甲脒类杀虫剂,也可能通过与章鱼胺受体相互作用而强烈激活脂肪体磷酸化酶。