Transcript Neurotox I
TOXC707 Advanced Toxicology (2007) Neurotoxicology: Overview: Factors unique to nervous system Examples of neurotoxicants Cells of the Nervous System ◄ neurons ◄ neuroglia (90% of cells) oligodendrocytes (Schwann cells in PNS) astrocytes microglia gliosis is a marker of gross CNS toxicity Increased expression of Glial Fibrillary Acidic Protein- (GFAP) Dopamine: A Brain Neuromodulator Frontal Cortex Gyrus Cinguli Corpus Callosum Basal Ganglia Nuc. Accumben s Olfactory Tubercle Hypothalamus } Sub. Nigra Tegmentum Pituitary Medial Forebrain Bundle Entorhinal Cortex Midbrain Types of neuronal connections Axons Axo-axonal Synapse Axo-somatic Synapse Perikarya Dendro-dendritic Synapse Axo-dendritic Synapse Dendrites Major Components of Peripheral Nervous System Peripheral neuron Three views of myelinating Schwann cell Nucleus Schwann cell cytoplasm Unwrapped Compact membrane (Myelin) Longitudinal Cross-section Cytoplasmic channel (SchmidtLantermann) Processes of demyelination and remyelination Susceptibility to neurotoxicants ◄ High metabolic rate and electrical excitability are dependent on membrane integrity and aerobic metabolism ◄ Extended length of axons poses logistical problems associated with transport from cell bodies to terminal fields ◄ Metabolism of some neurotransmitters may produce oxidative stress (e.g., dopamine) ◄ Inability to replace dead or dying cells Dr. Mailman’s Pet Peeves ◄ Neurotoxin A toxic compound of natural origin ◄ Neurotoxicant A toxic compound ◄ Putative “Generally regarded as such; supposed” (American Heritage) “Generally thought to be or to exist, whether or not this is really true” (Cambridge) Does not mean hypothesized or speculated. Consequences of neuronal characteristics ◄ axonal transport sensitive to toxicants ◄ hexanes cause cross-linking of neurofilaments ◄ diabetic neuropathy Neurodevelopmental Toxicology Unique aspects of the nervous system for neurotoxicology: Neurodevelopment ◄ Massive loss of neurons during vertebrate development has been known for more than a century. Beard (1889) – loss of neuronal populations in fish (RohonBeard Neurons) Collin (1906) – death of many sensory and motor neurons in the chick embryo ~50% of Post-mitotic neurons die during normal development Clarke, Rogers & Cowan J. Comp. Neurol. 167: 125 (1976) Apoptotic neuronal death in the developing substantia nigra R. Burke. Cell Tiss. Res. 2004 Victor Hamburger: Peripheral Targets Regulate Cell Death led to NGF discovery Transcriptional regulation of apoptotic cell death Summary ◄ ◄ ◄ ◄ ◄ There is massive death of neurons, neuroprogenitors, and oligodendroglia in normal vertebrate development. This is largely regulated by access to limiting supplies of exogenous survival-promoting trophic factors. Survival is promoted largely by activation of Akt as well as Erks, and involves blockade of death pathways at multiple points. Developmental neuron death is transcription dependent. Induction of death involves multiple pro-apoptotic signaling pathways, some of which converge on induction of BH3domain proteins. Impact of neurodevelopment on toxicology ◄ ◄ ◄ ◄ ◄ The effects of toxicological insults may be temporally delayed, being expressed as a variety of alterations in development. The effects of toxicant exposure will be markedly affected not only by dose/concentration, but also by timing. Insults by the same dose/concentration at different times during development may result in markedly different sequelae. Extrapolation from animal models present an even greater challenge than usual because of species differences in developmental patterns. This will be discussed later re. Fetal Alcohol Syndrome and solvents. Toxicant Access and Metabolism Unique aspects of the nervous system for neurotoxicology: Blood-brain barrier ◄ ◄ ◄ The choroid plexus separates the blood from the cerebrospinal fluid, whereas the blood-brain barrier limits the influx of circulating substances into the immediate brain interstitial space. Blood brain barrier limits influx of circulating substances from capillaries into interstitial space Brain capillaries, unlike those in other tissues, are not fundamentally porous. ◄ Tight junctions between adjacent capillary endothelial cells Processes from adjacent cells (astrocytic end feet). A microperoxidase (molecular mass 1800 daltons) that is readily transverses capillaries in other tissues will not pass through capillaries in the brain. Carrier-mediated transport systems exist for entry of certain required molecules (e.g., hexoses, carboxylic acids, amino acids (separate ones for neutral, basic, and acidic amino acids), amines, and inorganic ions Breaching the barrier ◄ Generalizations for healthy brain Large molecules (large peptides and proteins) are excluded Polar molecules are excluded; nonpolar lipid-soluble molecules can penetrate more easily Specific transport systems may facilitate toxicant passage ◄ e.g., increased absorption of dimethyl mercury vs. inorganic mercury (Minamata disease) e.g., MPP+ (toxic metabolite of MPTP) does not cross the BBB e.g., elemental mercury forms complex with cysteine and is recognized by amino acid transporters as methionine Alterations in BBB substances that alter membrane function (organic solvents) brain edema bacterial meningitis Unique aspects of the nervous system for neurotoxicology: Toxicant metabolism ◄ Although some xenobiotic metabolic capacity exists in brain, the relative concentration is low compared to the liver or other tissues. ◄ Detoxification mechanisms in CNS have much lower capacity and diversity than in periphery. ◄ Can be important for specific toxicants. 2,4,5-trihydroxyphenylalanine is activated MPTP is activated Unique aspects of the nervous system for neurotoxicology: Plasticity ◄ ◄ ◄ The nervous system has a unique capacity to accommodate to change. These changes may sometimes mask, or even be caused by, neurotoxic insult. Interesting phenomena include: Desensitization Sensitization Up- and down-regulation Long-term potentiation and other types of synaptic plasticity Sprouting Neurotransmission Neurotransmission ◄ ◄ Relies on separation of positive and negative charges across membrane Ionic gradient depends on ATP-linked Na+/K+ pump at rest, interior more negatively charged following sufficient stimulus in dendritic region, unidirectional impulse flow along axon occurs role of ion channels ◄ voltage gated sodium voltage-gated potassium channels Electrochemical neurotransmission vs. electrical transmission Synapse ◄ Specialized structure for releasing and sensing small amounts of neurotransmitters ◄ Neurotransmitters ◄ Importance vs. neuromodulators to toxicologists toxicants may act directly at synaptic loci toxicants may indirectly alter synaptic function Synaptic Structure Synaptic targets for toxicants ◄ Neurotransmitter synthesis ◄ Neurotransmitter storage ◄ Neurotransmitter inactivation or degradation ◄ Neurotransmitter receptor binding ◄ Receptor-linked ◄ Pumping second messenger events or transport of ions ◄ Downstream synthesis) cellular function (e.g., nucleic acid Mechanisms of toxicity: Receptors Receptors and Signal Transduction 1 2 ligand R a bg a Ion E1 R ligand R bg E2 3 ligand 4 R ligand R R R R R nucleus E P P P P Toxicants acting directly on receptors ◄ morphine and codeine ◄ mescaline ◄ LSD (ergot-contaminated grain and medieval European cities and the Salem witch trials??). methylxanthines ◄ derivative of peyote cactus mescaline is believed to cause central actions via interactions with serotonin receptors ergot alkaloids ◄ alkaloids of the opium poppy that causes acute analgesic, antitussive, euphoric, emetic/antiemetic effects caffeine; theophylline are found in coffee and tea Adenosine receptor ligands plus phosphodiesterase inhibitors reserpine – VMAT2 ligand blocks vesicular monamine transporter in dopamine and serotonin neurons initial effect is massive release later effect is long term depletion Cholinergic toxins ◄ Snake neurotoxins a-bungarotoxin ◄ Belladonna alkaloids ◄ atropine; scopolamine derived from “deadly nightshade” (Belladonna sp.) competitively blocks muscarinic cholinergic receptors also used as antidote for muscarinic agonists/ACh overactivity nicotine ◄ blocks nicotinic acetylcholine receptor (binds irreversibly) nAChR agonist Cholinesterase inhibitors solanine and chaconine (Solanum sp., tomoato, potato) Huperzine A physostigmine (eserine) from Calabar bean Clostridium Indirect Actions ◄ Tetanus ◄ Botulism ◄ Cl. tetani produces 70,000 KDa protein called tetanospasmin Blocks inhibitory synaptic input on spinal motor neurons, resulting in spastic paralysis. moved through nerve cells via retrograde axonal transport until it binds, or is fixed, to gangliosides in the brain stem or cord. Ricin also retrogradely transported. Cl. botulinum produces a series of neurotoxins Bind to presynaptic cholinergic nerve terminals Gas gangrene Cl. perfringens Amino acid receptors ◄ strychnine blocks glycine receptors in spinal cord predominantly effects due to blockade of normal inhibitory influence of glycine receptor complex ◄ monosodium glutamate (MSG) sodium salt of amino acid glutamate can be actively transported into brain Ion channel ligands ◄ Alteration in sodium channel activity tetrodotoxin (isolated from puffer fish) and saxitoxin (dinoflaggelate phytoplankton) veratridine steroidal alkaloid (found in Veratrum and Zygadenus species) depolarizes nerve membranes. grayanotoxins (plant alkaloids from leaves of Ericaceae family) ◄ binds to voltage-dependent sodium channel and blocks increases in conductance disrupts generation of action potentials causes reversible increase in Na+ channel permeability Ouabain inhibits Na+K+ ATPase by high affinity binding to a site on the enzyme interferes with maintenance of electrical potential across membrane Agents that disrupt calcium homeostasis ◄ ◄ In addition to effects on Na+ channels, pyrethroid insecticides target Ca2+/Mg2+ ATPase and calmodulin inhibition of these enzymes increases intracellular calcium excessive intracellular calcium is linked to a variety of deleterious effects Among other effects, a variety of heavy metals (lead, mercury, aluminum) are associated with increased intracellular calcium actions may derive from competition for binding sites on various types of calcium binding proteins Agents that alter intracellular signaling ◄ ◄ Mercury has ubiquitous effects e.g., interferes with synthesis of tubulin and other proteins mechanism my be its ability to couple to cysteine and other thiolcontaining groups, promoting binding to many proteins Aluminum competes with iron for cellular uptake due to similar coordination chemistry participates in redox cycling and oxygen radical formation promotes aggregation of certain proteins has been linked to pathogenesis of Alzheimer’s disease (AD) presence of aluminum in neurofibrillary tangles may be a consequence, not a cause of AD Agents that cause hypoxia ◄ ◄ ◄ ◄ Any agent that derives CNS of oxygen is neurotoxic Neuronal subpopulations with very metabolic activity are particularly susceptible (e.g., hippocampus, neocortex) Sequelae of hypoxia are similar to excitotoxicity Anoxic hypoxia (compromised oxygen supply to brain despite adequate blood flow) ◄ Ischemic hypoxia (block of blood supply to brain) ◄ carbon monoxide any agent causing cardiovascular failure (digitalis glycosides) Cytotoxic hypoxia (interference with cellular respiration) cyanide azide Agents that affect membranes ◄ Organic and inorganic lead damage membranes probably occurs via disruption of ion channels results in ultrastructural damage to mitochondria, breakdown of active transport, damage to myelincontaining membranes ◄ Copper can participate in formation of reactive oxygen species and lipid peroxidation ◄ Solvents and vapors are lipid soluble and can alter membrane fluidity Indirect effects on neurotransmission ◄ activation of neurotransmitter release latrotoxin (black widow venom) releases vesicle-bound neurotransmitters amphetamine, methamphetamine, ephedrine release catecholamines methylmercury neurotransmitter release occurs secondary to altered calcium homeostasis ◄ inhibition of neurotransmitter reuptake or metabolism organophosphates inhibit acetylcholinesterase Agents that interfere with oxidative phosphorylation ◄ Classical inhibitors of oxidative phosphorylation dinitrophenol cyanide hydrogen sulfide ◄ Lead, mercury and other metals indirectly compromise oxidative phosphorylation by mitochondrial insult ◄ MPTP directly inhibits oxidative phosphorylation Agents that damage myelin ◄ Some demyelinating agents do not cross BBB and demyelinate only in periphery ◄ Other agents of capable of CNS and PNS effects Hexachlorophene Isoniazid Tellurium Organotins Protection from oxidative damage ◄ ◄ ◄ Brain has highest rate of oxidative activity of any organ Endogenous oxygen-derived radicals are thought to be important in pathogenesis of many neurodegenerative diseases Both neurons and glia contain protective mechanisms; neurons benefit from secreted enzymes manufactured in glia ◄ e.g., glutathione is distributed ubiquitously--chelates transition metals and prevents redox cycling events glutathione peroxidase and superoxide dismutase are present in astrocytes catalase is found in oligodendrocytes The cytochrome P450 isozymes found in brain purported to have a role in Parkinson’s disease Discussion Translational Medicine (Buzzzzzzz): How can we assess neurotoxicity?