Metabolic changes in deafferented central neurons of an insect, Acheta domesticus. II. Effects on cholinergic binding sites and acetylcholinesterase

• Published in: The Journal of neuroscience 1986-06, Vol.6 (6), p.1676-1684
• Main Authors: Meyer, MR, Reddy, GR, Edwards, JS
• Format: Article
• Language: English
• Subjects: abdominal ganglia; acetylcholine; acetylcholinesterase; Acetylcholinesterase - metabolism; Acheta domesticus; Biochemistry. Physiology. Immunology; Biological and medical sciences; Denervation; Fundamental and applied biological sciences. Psychology; Gryllidae; Gryllidae - metabolism; Insecta; Invertebrates; Neurons, Afferent - metabolism; Physiology. Development; receptors; Receptors, Cholinergic - metabolism; Receptors, Muscarinic - metabolism; Receptors, Nicotinic - metabolism
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/jneurosci.06-06-01676.1986

Following the finding that cercal deafferentation of developing giant interneurons in the terminal abdominal ganglion (TG) of the cricket Acheta domesticus reduces TG protein metabolism within target interneuron dendrites and somata (Meyer and Edwards, 1982), it is now shown that deafferentation alters the turnover of three macromolecules associated with cholinergic transmission in the cercal sensory-giant interneuron pathway. The labeled specific ligands 3H-quinuclidinyl benzilate and 125I-alpha-bungarotoxin were used to assay populations of putative TG muscarinic and nicotinic cholinergic receptors, respectively, in control and deafferented groups of ganglia. The AChE activity of TG was also determined by assay and histochemical methods. Long-term deafferentation sustained throughout postembryonic development markedly reduces the densities of both muscarinic and nicotinic binding sites in the TG; short-term deafferentation of adult TG also leads to characteristic alterations in the properties of all three cholinergic markers within several days. Rapid changes seen in adults thus correlate with ultrastructural data demonstrating loss of afferent terminals within hours of sensory appendage removal. We propose that peripheral innervation-dependent regulatory mechanisms operate in both the developing and adult insect nervous system. Such mechanisms may influence transsynaptically the synthesis and turnover of specific macromolecules, some of which may reside on the cell surface of insect central neurons that are part of the cercal sensory-giant interneuron system.