Sekimizu Kazuhisa, Larranaga Jorge, Hamamoto Hiroshi, Sekine Masae, Furuchi Takemitsu, Katane Masumi, Homma Hiroshi, Matsuki Norio
Graduate School of Pharmaceutical Sciences, The University of Tokyo, 3-1 Hongo 7-chome, Bunkyo-ku, Tokyo 113-0033.
J Biochem. 2005 Feb;137(2):199-203. doi: 10.1093/jb/mvi019.
Agonists for muscle contraction in silkworms were screened by injecting test solutions into the hemolymph of decapitated silkworm larvae. Kainic acid, a glutamate receptor agonist, and D-glutamic acid induced muscle contractions, and D-aspartic acid was partially effective, whereas NMDA and AMPA, representative mammalian glutamate receptor agonists, did not induce contraction. L-Glutamic acid inhibited the kainic acid or D-glutamic acid-induced contraction. Amino acid analysis revealed that 3% of the total glutamic acid in the silkworm hemolymph is D-glutamic acid. These results suggest that d-glutamic acid acts physiologically as an agonist for muscle contraction in silkworms, and that L-glutamic acid functions as an inhibitor.
通过向断头家蚕幼虫的血淋巴中注射测试溶液,筛选家蚕肌肉收缩的激动剂。谷氨酸受体激动剂 kainic 酸和 D-谷氨酸可诱导肌肉收缩,D-天冬氨酸部分有效,而典型的哺乳动物谷氨酸受体激动剂 NMDA 和 AMPA 则不会诱导收缩。L-谷氨酸可抑制 kainic 酸或 D-谷氨酸诱导的收缩。氨基酸分析显示,家蚕血淋巴中总谷氨酸的 3% 是 D-谷氨酸。这些结果表明,D-谷氨酸在生理上作为家蚕肌肉收缩的激动剂起作用,而 L-谷氨酸则起抑制剂的作用。