Trimethyltin alters membrane properties of CA1 hippocampal neurons

• Published in: Neurotoxicology (Park Forest South) Vol. 13; no. 3; p. 569
• Main Authors: Harkins, A.B. (University of Texas at San Antonio, San Antonio, TX), Armstrong, D.L
• Format: Journal Article
• Language: English
• Published: Netherlands 1992
• Subjects: ACTION POTENTIAL; Action Potentials - drug effects; ANIMAL TISSUES; Animals; BRAIN; Cell Membrane - drug effects; CEREBRO; COMPOSE ORGANOSTANNIQUE; COMPUESTO ORGANICO DEL ESTANO; ELECTROPHYSIOLOGY; ENCEPHALE; HIPPOCAMPUS; Hippocampus - cytology; Hippocampus - drug effects; In Vitro Techniques; Male; MEMBRANA; MEMBRANE; MEMBRANE POTENTIAL; MEMBRANES; Microelectrodes; NERF; NERVES; NERVIOS; NERVOUS SYSTEM; Neurons - drug effects; NEUROTOXINS; ORGANOTIN COMPOUNDS; Organotin Compounds - toxicity; RAT; RATA; RATS; Rats, Sprague-Dawley; SISTEMA NERVIOSO; SYSTEME NERVEUX; TEJIDOS ANIMALES; TISSU ANIMAL; TOXICIDAD; TOXICITE; TOXICITY; TOXINAS; TOXINE; TOXINS; Trimethyltin Compounds - toxicity
• ISSN: 0161-813X; 1872-9711

Trimethyltin produces pathological changes in the hippocampus, but the physiological mechanisms underlying its toxicity remain unclear. Intracellular recordings of CA1 neurons in rat hippocampal slices were conducted during bath application of 50 and 100 microM trimethyltin and 50 and 200 microM dimethyltin. Trimethyltin slowly depolarized the membrane potential without spontaneous spiking, and decreased input resistance and time constant. Trimethyltin decreased, in a dose-dependent manner, both the elicited action potential and the orthodromically-stimulated action potential amplitudes; increased the threshold current for both elicited and orthodromically-stimulated action potentials; and prolonged the duration of the orthodromic excitatory post-synaptic potential. These trimethyltin-induced effects were not readily reversed. On the other hand, dimethyltin at high concentrations only reduced the amplitude of the orthodromic action potential. Slice viability was compromised following exposure to trimethyltin, but not following dimethyltin. These data demonstrate that decreased membrane time constant and input resistance is an early and reliable indicator of the onset of trimethyltin-induced changes. The effects do not resemble those produced by excitotoxins, but rather share similarities with responses observed during slice hypoxia.