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1.
Int J Neurosci ; : 1-7, 2020 Sep 23.
Article in English | MEDLINE | ID: mdl-32916077

ABSTRACT

PURPOSE/AIM: The role of cholinergic neurotransmission in the hippocampus remains controversial since different studies showed either no influence or its modulatory effect on glutamatergic hippocampal synapses. It remains unclear whether septal cholinergic input can modulate plasticity of synapses formed by CA3 pyramids on CA1 neurons. The aim of the study was to clarify the role of septal input in the development of LTP in this synapse. MATERIALS AND METHODS: We recorded in vivo in rats under urethane anesthesia focal excitatory postsynaptic potential (fEPSP) characteristics in CA1 area after stimulation of the ventral hippocampal commissure (VHC), which contains both CA3 axons innervating CA1 neurons and cholinergic axons coming from the medial septum. We performed two series of experiments in which LTP was induced by tetanization of either VHC or medial septal area (MSA). Degeneration of cholinergic neurons in MSA was induced by intraseptal injection of 192IgG-saporin. RESULTS: In both experimental series, tetanization induced an increase in fEPSP amplitude which lasted for at least 40 min after tetanic stimulation, although tetanization of VHC induced a larger increase in fEPSP amplitude compared to MSA tetanization. Elimination of septal cholinergic neurons by 192IgG-saporin abolished LTP development in both experimental series. This suppression of LTP in animals with cholinergic deficit was not due to loss of hippocampal neurons. CONCLUSIONS: Our data suggest that activation of septal cholinergic fibers during tetanization is a critical factor of LTP induction in the hippocampal CA3 to CA1 synapses.

2.
Biochemistry (Mosc) ; 82(10): 1088-1102, 2017 Oct.
Article in English | MEDLINE | ID: mdl-29037130

ABSTRACT

In this review, recent data are presented on molecular and cellular mechanisms of pathogenesis of the most widespread (about 95%) sporadic forms of Alzheimer's disease obtained on in vivo rodent models. Although none of the available models can fully reproduce the human disease, several key molecular mechanisms (such as dysfunction of neurotransmitter systems, especially of the acetylcholinergic system, ß-amyloid toxicity, oxidative stress, neuroinflammation, mitochondrial dysfunction, disturbances in neurotrophic systems) are confirmed with different models. Injection models, olfactory bulbectomy, and senescence accelerated OXYS rats are reviewed in detail. These three approaches to in vivo modeling of sporadic Alzheimer's disease have demonstrated a considerable similarity in molecular and cellular mechanisms of pathology development. Studies on these models provide complementary data, and each model possesses its specific advantages. A general analysis of the data reported for the three models provides a multifaceted and the currently most complete molecular picture of sporadic Alzheimer's disease. This is highly relevant also from the practical viewpoint because it creates a basis for elaboration and preclinical studies of means for treatment of this disease.


Subject(s)
Alzheimer Disease/pathology , Acetylcholinesterase/metabolism , Alzheimer Disease/metabolism , Amyloid beta-Peptides/metabolism , Animals , Brain/drug effects , Brain/metabolism , Ciliary Neurotrophic Factor/genetics , Ciliary Neurotrophic Factor/metabolism , Disease Models, Animal , Endotoxins/toxicity , Olfactory Bulb/surgery , Oxidative Stress
3.
Biochemistry (Mosc) ; 82(3): 275-281, 2017 Mar.
Article in English | MEDLINE | ID: mdl-28320268

ABSTRACT

Infectious diseases in early postnatal ontogenesis can induce neuroinflammation, disrupt normal central nervous system development, and contribute to pathogenesis of cerebral pathologies in adults. To study long-term consequences of such early stress, we induced neonatal proinflammatory stress (NPS) by injecting bacterial lipopolysaccharide into rat pups on postnatal days 3 and 5 and then assessed the levels of corticosterone, proinflammatory cytokines and their mRNAs, and neurotrophins and their mRNAs in the hippocampus and neocortex of the one-month-old animals. Long-term potentiation (LTP) was studied in hippocampal slices as an index of synaptic plasticity. NPS-induced impairments of LTP were accompanied by the accumulation of corticosterone and IL-6 in the hippocampus. In the neocortex, a decrease in exon IV BDNF mRNA was detected. We suggest that excessive corticosterone delivery to hippocampal receptors and proinflammatory changes persisting during brain maturation are among the principal molecular mechanisms responsible for NPS-induced neuroplasticity impairments.


Subject(s)
Corticosterone/metabolism , Hippocampus/metabolism , Interleukin-6/metabolism , Long-Term Potentiation , Neuronal Plasticity , Stress, Physiological , Animals , Hippocampus/pathology , Inflammation/metabolism , Inflammation/pathology , Male , Rats , Rats, Wistar
4.
Zh Vyssh Nerv Deiat Im I P Pavlova ; 66(5): 611-625, 2016 09.
Article in Russian | MEDLINE | ID: mdl-30695406

ABSTRACT

We studied the effect of chronic combined stress (model of experimental neurosis) on behavior of rats with different basal strategies of behavior in novelty conditions. Chronic stress resulted in decreases in the body weight and testosterone contents in the blood and neocortex in all animals. Animals with initially low orient- ing-exploratory response in the "open field" test did not exhibit substantial alterations of behavior during repeated testing in this test of the "dark-light chamber" test; however, the depression-like behavior was more expressed in the second forced swim test. Chronic combined stress did not significantly affect the behavior of this group of rats. Animals with initially high orienting-exploratory response in the "open field" test exhibited decreased locomotor and exploratory activity in the repeated "open field" tests. The decreases in the locomotor and exploratory activity were substantially less expressed in the repeated tests in these rats after chronic combined stress. The indices of depression-like behavior increased one month after the end of exposure to chronic combined stress. Our data demonstrate that different responses to novelty in the "open field" test do not allow predict with reasonable certainty the development of depression-like behavior after exposure to chronic combined stress.


Subject(s)
Anxiety/physiopathology , Depressive Disorder/physiopathology , Exploratory Behavior/physiology , Stress, Psychological/physiopathology , Animals , Anxiety/blood , Behavior, Animal/physiology , Body Weight , Depressive Disorder/blood , Disease Models, Animal , Locomotion/physiology , Male , Neocortex/metabolism , Neocortex/physiopathology , Rats , Rats, Wistar , Stress, Psychological/blood , Swimming , Testosterone/blood
5.
Zh Vyssh Nerv Deiat Im I P Pavlova ; 66(5): 632-640, 2016 09.
Article in Russian | MEDLINE | ID: mdl-30695408

ABSTRACT

Opiate reinforcement is considered as a stimulus inducing addiction, however underlying neurobiological mechanisms remain obscure. According to the literature, BDNF (brain-derived neurotrophic factor) in the lateral ventral tegmental area (VTA) could modulate morphine reinforcement, but the role of BDNF in the midline VTA has not been studied yet. The aim of the study was to investigate the effect of a single intra-mid- line VTA injection on the acquisition and expression of morphine conditioned place preference (CPP). CPP procedure was composed of eight conditioning sessions (one session per day): morphine (i.p., 10 mg/kg) and saline injections were paired to the compartments and counterbalanced.Recombinant human BDNF (0.75 ug) or phosphate-buffered saline (PBS) as a vehicle were injected once into the midline VTA one day before or after conditioning. According to the CPP test rats spent more time in the morphine-paired compartments a scompared to the saline-paired compartments (p < 0.05). After a single BDNF injection into the midline VTA be- fore conditioning, but not after conditioning, differences in time spent in morphine and saline-paired compartments did not reach significance (p > 0.05). Thus, taking into account limitations of the results, we sug- gest that BDNF in the midline VTA may block morphine reinforcement.


Subject(s)
Brain-Derived Neurotrophic Factor/pharmacology , Conditioning, Classical/drug effects , Morphine/pharmacology , Narcotics/pharmacology , Reinforcement, Psychology , Ventral Tegmental Area/drug effects , Animals , Choice Behavior/drug effects , Conditioning, Classical/physiology , Electrodes, Implanted , Humans , Injections, Intraperitoneal , Injections, Intraventricular , Male , Rats , Rats, Wistar , Saline Solution/pharmacology , Stereotaxic Techniques , Ventral Tegmental Area/physiology
6.
Morfologiia ; 148(5): 14-20, 2015.
Article in Russian | MEDLINE | ID: mdl-26987212

ABSTRACT

Using dosed lateral fluid percussion, moderate and severe traumatic brain injury (TBI) was modeled in one- and two-year-old rats. Brain sections were stained using the Nissl cresyl violet method and an immunohistochemical reaction was performed for the demonstration of glial fibrillary acidic protein (GFAP), a marker of astrocytes. The results obtained indicate the formation in the cerebral cortex, ipsilateral to the impact, the zones of direct and remote of injury. The zone of direct injury corresponded to the area of immediate contact of the liquid column with the dura mater, whereas the remote area of damage was located laterally and caudally to the former. Morphological signs of the injury depended on the force of impact and were manifested in both age groups by astrocytic gliosis and the thinning of layer I of the cortex resulting from neuronal death. The emergence of ischemia-modified neurons, probably, was due to a local disruption of the blood supply. Disorders in the brain in one-year-old rats had a local character and those in two-year-old rats were diffuse, while gliosis was inhomogeneous. The reproducibility and adequacy of the model allow its use for research of molecular-genetic mechanisms of TBI outcomes in humans, as well as for the identification of common mechanisms of TBI consequences and the pathogenesis of the major diseases, comorbid with TBI, primarily depression and epilepsy.


Subject(s)
Aging , Brain Injuries , Cerebral Cortex , Aging/metabolism , Aging/pathology , Animals , Brain Injuries/metabolism , Brain Injuries/pathology , Cerebral Cortex/metabolism , Cerebral Cortex/pathology , Male , Rats , Rats, Wistar
7.
Bull Exp Biol Med ; 153(6): 835-8, 2012 Oct.
Article in English, Russian | MEDLINE | ID: mdl-23113297

ABSTRACT

We studied the expression of mRNA for genes, whose protein products regulate the glutamate/NO/cGMP signal cascade in the frontal cortex, striatum, midbrain, and hippocampus of rats with various degrees of spontaneous morphine withdrawal syndrome. The concentration of Grin2a mRNA (subunit of the NMDA glutamate receptor) in the frontal cortex increased mainly in animals with severe abstinence. By contrast, the expression of mRNA for the Grin2b subunit in the striatum decreased in animals with mild abstinence. Variations in the content of mRNA for other products of the cascade (isoforms of NO-dependent guanylate cyclase and cGMP-dependent protein kinase) after morphine withdrawal were not related to the degree of abstinence. Our results suggest that the region-specific expression of mRNA for certain subunits of the NMDA glutamate receptor after morphine withdrawal can determine the degree of abstinence.


Subject(s)
Corpus Striatum/metabolism , Frontal Lobe/metabolism , Morphine Dependence/genetics , RNA, Messenger/genetics , Receptors, N-Methyl-D-Aspartate/genetics , Substance Withdrawal Syndrome/genetics , Animals , Corpus Striatum/physiopathology , Cyclic GMP-Dependent Protein Kinases/genetics , Cyclic GMP-Dependent Protein Kinases/metabolism , Frontal Lobe/physiopathology , Gene Expression , Guanylate Cyclase/genetics , Guanylate Cyclase/metabolism , Isoenzymes/genetics , Isoenzymes/metabolism , Male , Morphine/adverse effects , Morphine Dependence/etiology , Morphine Dependence/metabolism , Morphine Dependence/physiopathology , Nitric Oxide/metabolism , Organ Specificity , RNA, Messenger/metabolism , Rats , Rats, Wistar , Receptors, N-Methyl-D-Aspartate/metabolism , Severity of Illness Index , Signal Transduction , Substance Withdrawal Syndrome/metabolism , Substance Withdrawal Syndrome/physiopathology
8.
Epilepsy Behav ; 22(3): 433-41, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21907628

ABSTRACT

There are increasing data on the influence of seizures on neurogenesis in the adult brain. However, data on cell proliferation and differentiation during the early stages of kindling are scarce. We have used pentylenetetrazole (PTZ)-induced kindling to investigate the temporal profile of cytogenesis in the germinative zones of adult rat brain. For comparison, we also used a single PTZ-induced generalized tonic-clonic seizure. During kindling development, the density of 5-bromo-2'-deoxyuridine-positive cells demonstrated similar changes in all germinative zones: a dramatic decrease after the first subthreshold PTZ injection, and a gradual increase to the control level following repeated PTZ administration. On the contrary, a single PTZ-induced generalized tonic-clonic seizure was followed by an increase in the number of proliferating cells in both the dentate gyrus and the subventricular zone. These results may indicate the existence of global mechanisms affecting cellular proliferation in adult brain during seizures. Different temporal profiles of neuronal damage and proliferation changes suggest that neurodegeneration is unlikely to be a global proliferation-regulating factor. The data may contribute to better understanding of the initial phase of kindling development and epileptogenesis.


Subject(s)
Cell Proliferation/drug effects , Convulsants/toxicity , Hippocampus/pathology , Kindling, Neurologic/drug effects , Pentylenetetrazole/toxicity , Seizures/chemically induced , Animals , Bromodeoxyuridine/metabolism , Cell Count , Disease Models, Animal , Dose-Response Relationship, Drug , Hippocampus/drug effects , Kindling, Neurologic/pathology , Male , Rats , Rats, Wistar , Seizures/pathology , Statistics, Nonparametric , Time Factors
9.
Bull Exp Biol Med ; 149(2): 201-3, 2010 Aug.
Article in English, Russian | MEDLINE | ID: mdl-21113491

ABSTRACT

We studied the effects of afobazole on apoptosis through active caspase-3. Afobazole in a final concentration of 10(-8) M inhibits hyperactivation of effector apoptotic caspase-3 in HT-22 cell culture under conditions of glutamate toxicity.


Subject(s)
Anti-Anxiety Agents/pharmacology , Apoptosis/drug effects , Benzimidazoles/pharmacology , Caspase 3/metabolism , Glutamic Acid/metabolism , Morpholines/pharmacology , Animals , Bisbenzimidazole , Cell Line , Glutamic Acid/toxicity , Mice , Microscopy, Fluorescence , Octoxynol
10.
Neurosci Behav Physiol ; 40(2): 123-6, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20033317

ABSTRACT

The effects of intracerebroventricular administration of fragment (25-35) of beta-amyloid peptide [Abeta(25-35)] on cell proliferation in the subventricular zone of the dentate gyrus of the hippocampus in adult rats were analyzed. Animals received doses of 15 nmol of pre-aggregated Abeta(25-35) or the Abeta(35-25) control peptide, or solvent (sterile water) into the lateral ventricles. On post-injection days 1-5, rats received intraperitoneal injections of the thymidine analog 5-bromo-2'-deoxyuridine (BrdU). BrdU incorporated into DNA was detected immunohistochemically on frontal brain sections six and 12 days after peptide administration. At six days, the numbers of BrdU-containing cells in the subventricular zone showed no differences between the study groups. At 12 days, the total number of BrdU-positive cells decreased significantly in all study groups. At the same time, the number of labeled cells in rats given Abeta(25-35) was significantly greater in this brain zone than in animals given water or the control peptide. Thus, Abeta(25-35) significantly increased cell proliferation in the subventricular zone after intracerebroventricular administration.


Subject(s)
Amyloid beta-Peptides/metabolism , Cell Proliferation , Dentate Gyrus/physiology , Peptide Fragments/metabolism , Stem Cell Niche/physiology , Aging , Animals , Bromodeoxyuridine , Immunohistochemistry , Male , Protein Multimerization , Rats , Rats, Wistar , Time Factors
12.
Biochemistry (Mosc) ; 74(3): 281-7, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19364322

ABSTRACT

The cysteine proteases caspase-3 and cathepsins are involved in both neuronal plasticity and neuropathology. Using primary neuroglial and glial cerebellar cultures, the pH dependence of cleavage of a synthetic caspase-3 substrate, Ac-DEVD-AMC, was studied. At acidic pH, cathepsin B cleaved Ac-DEVD, this activity being significantly higher than that of caspase-3 at pH 7.4. This activity is blocked by peptide inhibitors of both caspase-3 and cathepsin B. Substitution of culture medium for balanced salt solution stimulated cathepsin B secretion in both types of cultures. Ischemia (oxygen-glucose deprivation) significantly decreased secretion of cathepsin B activities into the culture medium.


Subject(s)
Caspase 3/metabolism , Cathepsin B/metabolism , Coumarins/metabolism , Oligopeptides/metabolism , Animals , Caspase Inhibitors , Catalysis/drug effects , Cell-Free System/enzymology , Cells, Cultured , Culture Media/chemistry , Culture Media/pharmacology , Glucose/pharmacology , Hydrogen-Ion Concentration , Neuroglia/cytology , Neuroglia/enzymology , Oligopeptides/pharmacology , Oxygen/pharmacology , Rats , Rats, Wistar , Substrate Specificity , Time Factors
13.
Neurosci Behav Physiol ; 39(1): 65-72, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19089628

ABSTRACT

We have previously demonstrated transient increases in caspase-3 activity in the hippocampus of rat pups from age 17 days. We report here our studies on the effects of inhibition of caspase-3 during this period on the acquisition of a two-way avoidance reaction. Rat pups received intracerebroventricular doses of the caspase-3 inhibitor Z-DEVD-FMK On postnatal day 18. Control animals of the same age received the inactive peptide Z-FA-FMK or isotonic saline solution. Inhibition of caspase-3 during the period of its natural activation in the hippocampus during early ontogenesis was found to impair the development of operant behavior in rats. This was apparent as a reduction in the efficiency of learning during acquisition of active avoidance reactions and decreases in the numbers of intersignal reactions. Administration of the inhibitor had no specific action on the types of conditioned reflex activity less associated with operant learning. Thus, there were no differences between the experimental and control groups in the numbers of emotional reactions to the conditioned stimulus. The number of orientational-investigative conditioned reactions also showed no change after administration of Z-DEVD-FMK. On the background of the reduction in the efficiency of the acquisition of the conditioned active avoidance reflex, the number of incomplete acts, in contrast to other types of conditioned reactions, increased significantly after administration of Z-DEVD-FMK, which is evidence for the persistence of the ability to form associative connections between activation of the conditioned signal and the need to move to the other sector. The difficulty in these animals arose at the decision-taking stage on choosing the appropriate form of behavior. Changes in orientational-investigative behavior were not associated with inhibition of caspase-3 during the critical period of development, as the effects of Z-DEVD-FMK and Z-FA-FMK were similar.


Subject(s)
Caspase 3/metabolism , Conditioning, Operant/physiology , Hippocampus/enzymology , Animals , Caspase Inhibitors , Conditioning, Operant/drug effects , Enzyme Activation , Escape Reaction/drug effects , Escape Reaction/physiology , Female , Hippocampus/growth & development , Male , Oligopeptides/pharmacology , Rats , Rats, Wistar
14.
Neurosci Behav Physiol ; 36(7): 741-8, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16841155

ABSTRACT

Structural changes in neurons and measures of oxidative stress were studied in the hippocampus of rats tolerant (ST) and sensitive (SS) to developing clonic-tonic seizures in conditions of pentylenetetrazol kindling. Sequences of 11 injections of pentylenetetrazol significantly decreased the number of normal neurons in hippocampal field CA1 in SS rats, this effect being seen in both hippocampal field CA1 and the dentate fascia in ST rats. Decreases in the numbers of normal neurons were accompanied by increases in the numbers of damaged cells in field CA4 in rats of both groups. After 21 injections, decreases in the numbers of normal neurons were seen in field CA1 in both SS and ST rats, while the numbers of damaged neurons were significantly greater than control only in ST rats in fields CA1 and CA4. The glutathione level was significantly lower in the hippocampus in both groups of rats than in controls. Thus, rats " tolerant" to developing convulsions show signs of oxidative stress and neurodegenerative changes in the hippocampus. This suggests that oxidative neuron damage leading to neurodegeneration in the pentylenetetrazol kindling model is not directly associated with convulsive activity.


Subject(s)
Hippocampus/pathology , Kindling, Neurologic/pathology , Nerve Degeneration/pathology , Neurons/pathology , Seizures/pathology , Animals , Cell Count , Convulsants , Male , Nerve Degeneration/chemically induced , Oxidative Stress/drug effects , Pentylenetetrazole , Rats , Rats, Wistar , Seizures/chemically induced , Statistics, Nonparametric
15.
Eur J Neurosci ; 23(1): 129-40, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16420423

ABSTRACT

Although caspase activity in the nervous system of mollusks has not been described before, we suggested that these cysteine proteases might be involved in the phenomena of neuroplasticity in mollusks. We directly measured caspase-3 (DEVDase) activity in the Helix lucorum central nervous system (CNS) using a fluorometrical approach and showed that the caspase-3-like immunoreactivity is present in the central neurons of Helix. Western blots revealed the presence of caspase-3-immunoreactive proteins with a molecular mass of 29 kDa. Staurosporin application, routinely used to induce apoptosis in mammalian neurons through the activating cleavage of caspase-3, did not result in the appearance of a smaller subunit corresponding to the active caspase in the snail. However, it did increase the enzyme activity in the snail CNS. This suggests differences in the regulation of caspase-3 activity in mammals and snails. In the snail CNS, the caspase homolog seems to possess an active center without activating cleavage typical for mammals. In electrophysiological experiments with identified snail neurons, selective blockade of the caspase-3 with the irreversible and cell-permeable inhibitor of caspase-3 N-benzyloxycarbonyl-Asp(OMe)-Glu(OMe)-Val-Asp-(OMe)-fluoro-methylketone prevented development of the long-term stage of synaptic input sensitization, suggesting that caspase is necessary for normal synaptic plasticity in snails. The results of our study give the first direct evidence that the caspase-3-like activity is essential for long-term plasticity in the invertebrate neurons. This activity is presumably involved in removing inhibitory constraints on the storage of long-term memory.


Subject(s)
Caspases/metabolism , Central Nervous System/cytology , Neuronal Plasticity/physiology , Neurons/cytology , Neurons/physiology , Synapses/physiology , Animals , Apoptosis/drug effects , Blotting, Western/methods , Caspase 3 , Caspases/pharmacology , Central Nervous System/physiology , Drug Interactions , Enzyme Inhibitors/pharmacology , Gene Expression/drug effects , Helix, Snails , Immunohistochemistry/methods , In Situ Nick-End Labeling/methods , In Vitro Techniques , Neuronal Plasticity/drug effects , Neuronal Plasticity/radiation effects , Neurons/classification , Oligopeptides/pharmacology , Staurosporine/pharmacology , Synapses/drug effects , Synapses/radiation effects
16.
Neurosci Behav Physiol ; 36(1): 101-6, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16328175

ABSTRACT

The possible link between amnesia induced by central administration of beta-amyloid (25-35) (Abeta(25-35)) and neurodegenerative changes in the hippocampus was studied. Male Wistar rats received single intracerebroventricular injections of Abeta(25-35) at a dose of 15 nmoles and one month later were trained in an eight-arm radial maze. Training was followed by histological assessment of the state of the hippocampus on brain sections stained with hematoxylin and eosin. Abeta(25-35) induced impairments in long-term (reference) and working memory on testing in the maze. There was a moderate reduction in the number of neurons in hippocampal field CA1; there was no change in the number of cells in field CA3. The numbers of errors made by the animals on testing in the maze were found to correlate negatively with the numbers of nerve cells in hippocampal field CA1. Thus, this is the first demonstration that impairments of learning and memory induced by single doses of Abeta(25-35) are specifically associated with neurodegenerative changes in hippocampal field CA1 in rats.


Subject(s)
Amyloid beta-Peptides/toxicity , Hippocampus/drug effects , Memory Disorders/chemically induced , Memory Disorders/pathology , Peptide Fragments/toxicity , Animals , Behavior, Animal/drug effects , Cell Count , Hippocampus/pathology , Injections, Intraventricular/methods , Male , Maze Learning/drug effects , Maze Learning/physiology , Memory Disorders/physiopathology , Neurons/pathology , Rats , Rats, Wistar
17.
Neuroscience ; 136(2): 579-91, 2005.
Article in English | MEDLINE | ID: mdl-16198488

ABSTRACT

Recent studies suggest that caspase-3-mediated mechanisms are essential for neuronal plasticity. N-benzyloxycarbonyl-Asp(OMe)-Glu(OMe)-Val- Asp(OMe)-fluoromethyl ketone (z-DEVD-fmk), a caspase inhibitor with predominant specificity toward caspase-3, has been shown to block long-term potentiation in hippocampal slices. Intrahippocampal infusion of a caspase-3 inhibitor to rats has been shown to significantly impair spatial memory in the water maze. The present work was designed to study whether i.c.v. administration of a caspase-3 inhibitor z-DEVD-fmk impairs learning in other tasks related to specific forms of memory in rats. The rats received bilateral injections of z-DEVD-fmk or N-benzyloxycarbonyl-Phe-Ala-fluoromethyl ketone (z-FA-fmk) ("control" peptide) at a dose of 3 nmol. Administration of z-DEVD-fmk significantly decreased the number of avoidance reactions in some blocks of trials in the active avoidance (shuttle box) learning, while z-FA-fmk had no effect as compared with intact rats. However, only a slight effect of the caspase inhibitor across the session was found. z-DEVD-fmk impaired development of some essential components of the two-way active avoidance performance, such as escape reaction, conditioned fear reaction, and inter-trial crossings. Measurement of caspase-3 activity in rat brain regions involved in active avoidance learning revealed most expressed z-DEVD-fmk-related inhibition of the enzyme activity (about 30%) in the fronto-parietal cortex. A similar effect was close to significant in the hippocampus, but not in the other cerebral structures studied. In primary cultures of cerebellar neurons z-DEVD-fmk (2-50 microM) inhibited caspase-3 activity by 60-87%. We suggest that moderate inhibition of caspase-3 resulting from the central administration of z-DEVD-fmk to rats may impair active avoidance learning. Taking into account previous data on the involvement of neuronal caspase-3 in neuroplasticity phenomena we assume that the enzyme may be important for selected forms of learning.


Subject(s)
Caspase Inhibitors , Conditioning, Operant/drug effects , Enzyme Inhibitors/pharmacology , Animals , Avoidance Learning/drug effects , Caspase 3 , Cells, Cultured , Cerebellum/cytology , Cerebellum/enzymology , Enzyme Inhibitors/administration & dosage , Injections, Intraventricular , Learning/drug effects , Male , Memory/drug effects , Oligopeptides/pharmacology , Peptide Hydrolases/chemistry , Peptide Hydrolases/metabolism , Protease Inhibitors/pharmacology , Rats , Rats, Wistar
18.
Neurosci Behav Physiol ; 35(5): 511-8, 2005 Jun.
Article in English | MEDLINE | ID: mdl-16033199

ABSTRACT

Decreases in cognitive functions, particularly long-term (episodic) and working memory, are among the earliest prognostic signs of Alzheimer's disease. The toxicity of beta-amyloid peptide is regarded as a major cause of neurodegeneration and cognitive impairment in this disease. The present report describes studies of the effects of intracerebroventricular administration of beta-amyloid peptide (25-35) (Abeta(25-35)) on the reproduction of a previously assimilated habit consisting of finding food in an eight-arm radial maze in rats. Abeta(25-35) was given bilaterally at doses of 15 and 30 nmol/animal seven days after preliminary training. Testing was performed 60 days after peptide administration. The results showed that Abeta(25-35) impaired working memory in rats without having any significant effect on the retention of responses. We were unable to demonstrate any relationship between memory impairment and the dose of peptide given. These data provide evidence of the ability of Abeta(25-35) to produce greater degradation of working memory function than long-term memory function.


Subject(s)
Amyloid beta-Peptides/pharmacology , Behavior, Animal/drug effects , Maze Learning/drug effects , Peptide Fragments/pharmacology , Animals , Dose-Response Relationship, Drug , Functional Laterality/drug effects , Injections, Intraventricular/methods , Male , Rats , Rats, Wistar , Reaction Time/drug effects , Retention, Psychology/drug effects , Time Factors
19.
Neurosci Behav Physiol ; 35(7): 715-21, 2005 Sep.
Article in English | MEDLINE | ID: mdl-16433067

ABSTRACT

The relationship between convulsive activity evoked by repeated electric shocks and structural changes in the hippocampus of Balb/C mice was studied. Brains were fixed two and seven days after the completion of electric shocks, and sections were stained by the Nissl method and immunohistochemically for apoptotic nuclei (the TUNEL method). In addition, the activity of caspase-3, the key enzyme of apoptosis, was measured in brain areas immediately after completion of electric shocks. The number of neurons decreased significantly in field CA1 and the dentate fascia, but not in hippocampal field CA3. The numbers of cells in CA1 and CA3 were inversely correlated with the intensity of convulsions. Signs of apoptotic neuron death were not seen, while caspase-3 activity was significantly decreased in the hippocampus after electric shocks. These data support the notion that functional changes affect neurons after electric shock and deepen our understanding of this view, providing direct evidence that there are moderate (up to 10%) but significant levels of neuron death in defined areas of the hippocampus. Inverse correlations of the numbers of cells with the extent of convulsive activity suggest that the main cause of neuron death is convulsions evoked by electric shocks.


Subject(s)
Electroshock/adverse effects , Hippocampus/pathology , Neurodegenerative Diseases/pathology , Neurodegenerative Diseases/physiopathology , Neurons/radiation effects , Animals , Caspase 3 , Caspases/metabolism , Cell Count/methods , Cell Death/radiation effects , Disease Models, Animal , Female , Mice , Mice, Inbred BALB C , Neurodegenerative Diseases/etiology , Neurodegenerative Diseases/metabolism , Neurons/metabolism , Neurons/pathology
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