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Biomedical subjects

M A Persinger

Publications and source records attributed to M A Persinger.

At least 19 recordsLinked to original sources

Weak, physiologically patterned magnetic fields do not affect maze performance in normal rats, but disrupt seized rats normalized with ketamine: possible support for a neuromatrix concept?

The concept of a neuromatrix as a determinant of behavior proposes that complex neuroelectromagnetic patterns supported by specific spatial configurations of neurons underlie the generation of behaviors. When the pattern of neuronal connectivity is changed, as occurs during limbic epilepsy, neuroelectromagnetic patterns change in parallel to sustain behavioral output. Thus, a testable prediction of the neuromatrix concept is that the "normal" behaviors of animals with markedly reorganized neuroelectromagnetic patterns are vulnerable to specific stimuli that are ineffective when applied to a normal population. Because rats treated with ketamine after being induced to seize with pilocarpine exhibit behaviors indistinguishable from those of control populations despite marked changes in brain structure, they represent an ideal population in which to examine this hypothesis. Ketamine-treated pilocarpine-seized rats and normal rats were exposed continuously either to a complex sequence magnetic field or to control conditions during the acquisition of a radial arm maze task for 8 consecutive days. After 14 days of subsequent exposure to a frequency-modulated field (7-500 nT), during which time there was no training, the rats that had been induced to seize and had been exposed continuously to this magnetic configuration exhibited conspicuously slower response durations per arm than rats that had been induced to seize and exposed to control conditions or normal rats that had been exposed to either magnetic fields or control conditions. Thus, the behaviors of rats who have sustained multiple, discrete injuries throughout the brain may be seriously disrupted by the appropriate pattern of exogenous weak magnetic fields. Our results represent the first empirical support for the concept of the neuromatrix.

Analgesics↗

Extreme obesity in female rats following prepuberal induction of lithium-pilocarpine seizures and a single injection of acepromazine.

Seizures were induced in female Wistar albino rats at either 35 or 55 days of age with a single systemic injection of lithium (3 mEq/kg) and pilocarpine (30 mg/kg); the rats were then treated with the atypical neuroleptic acepromazine (25 mg/kg). These rats manifested progressive weight gain for the rest of their lives. The effect was conspicuous by casual observation 6 weeks after treatment and occurred primarily in those rats that later developed spontaneous seizures. After 1 year, the rats were obese (>1000 g). Such weight gains, associated with almost three times the serum triglyceride levels, were not observed in male rats and have not been observed in hundreds of female rats that received this treatment as adults. Single postseizure injections of ketamine rather than acepromazine did not produce this obesity; the weights of these rats were similar to those of normal littermates. These results indicate that a single injection of a neuroleptic during limbic seizures before puberty can produce neuronal alterations that contribute to a lifetime of obesity.

Acepromazine↗

Sucrose ingestion decreases seizure onset time in female rats treated with lithium and pilocarpine.

To extend previous work concerning diet and overt seizures in rats, we tested the hypothesis that ingestion of 10% sucrose-water could reduce seizure onset time (SOT) in rats given lithium and pilocarpine. We found that female but not male rats given free access to a 10% sucrose-water solution for 3 weeks exhibited shorter SOTs than age- and sex-matched control subjects. A separate experiment determined that SOT was significantly reduced whether female rats were provided 1, 2, 3, or 4 weeks of free access to sucrose. Moreover, the daily volume of sucrose ingested was significantly correlated (r=-0.42) with SOT regardless of the duration of sucrose treatment (in weeks). These findings suggest that a diet supplemented with sugar can facilitate the emergence of behavioral seizures in female rats given lithium and pilocarpine. We discuss the potential role of dopamine in mediating the sucrose-induced changes in SOT.

Animals↗

Reduced litter sizes following 48-h of prenatal exposure to 5 nT to 10 nT,0.5 Hz magnetic fields: implications for sudden infant deaths.

To test the hypothesis that a narrow intensity band of geomagnetic activity contributes to Sudden Infant Death, 32 pregnant rats were exposed for two to three days before expected parturition either to a coil that generated 0.5 Hz sine-wave, 5 to 10 nanoTesla magnetic fields, or to a reference coil (<1 nT) in the same room. The field was off for 30 min every 4 h during the exposure. The orientation of the coils was perpendicular in space and activated alternately in four blocks of experiments. The litters born to the exposed mothers contained significantly fewer pups (M = 14.1,SD= 2.1) than those exposed to the control conditions (M = 16.2, SD = 2.7). There were significantly fewer numbers of males and fewer numbers of females in litters exposed to the fields generated in the east-west and north-south directions, respectively. These results support the hypothesis that a specific temporal configuration of brief periods of geomagnetic activity can produce an increased incidence of nonvital fetuses, neonates, or infants.

Animals↗

Complex magnetic fields enable static magnetic field cue use for rats in radial maze tasks.

Male Wistar rats were trained in an eight-arm radial maze task (two sessions per day, delayed-non-matching-to-sample) that included an intramaze static magnetic field "cue" (185 microT) specific to the entrance point of one of the arms. Rats were exposed daily for 60 min to a complex magnetic field waveform (theta-burst pattern, 200-500 nT), presented with several different interstimulus intervals (ISIs), either immediately following training sessions or immediately preceding testing sessions. Application of the theta-burst stimulus with a 4000 ms ISI significantly improved the rats' memory for the arm of the radial maze whose position was indicated by the presence of a static magnetic field cue. Reference memory errors were homogeneously distributed among all eight arms of the maze for sham-exposed rats, and among the other seven arms of the maze for complex magnetic field-treated rats. These results suggest that static magnetic field cues may be salient orienting cues even in a microenvironment such as a radial maze, but their use as a cue during maze learning in rats is dependent on whole-body application of a specific time-varying complex magnetic field.

Animals↗

Increased feelings of the sensed presence and increased geomagnetic activity at the time of the experience during exposures to transcerebral weak complex magnetic fields.

In 2 separate experiments involving 39 subjects the incidence of sensing a presence or Sentient Being while being exposed to weak complex magnetic fields over the right hemisphere was moderately correlated with increased global geomagnetic activity during the 3-h periods of the experiences. Analyses of magnetometer values near the laboratory indicated the intensity of the east-west component of the geomagnetic field had been increasing consistently at about 1 pT/s for at least 10 min for a cumulative change of about 15 to 20 nT. The ratios of the durations of alpha rhythms over the temporal lobes compared to the occipital lobes were correlated significantly with both increased geomagnetic activity and the reports of a presence. Removal of the shared variance between the sensed presence and various psychometric inferences of temporal lobe sensitivity and the history of dissociation increased and decreased, respectively, the strength of the partial correlations between geomagnetic activity and the reports of a sensed presence. The results suggest the culturally and historically ubiquitous phenomena of sensed presences are generated by right hemispheric processes that once enhanced by a variety of stimuli, including weak complex magnetic fields, can be encouraged by increased global geomagnetic activity.

Adolescent↗

Sudden death in epileptic rats exposed to nocturnal magnetic fields that simulate the shape and the intensity of sudden changes in geomagnetic activity: an experiment in response to Schnabel, Beblo and May.

To test the hypothesis that sudden unexplained death (SUD) in some epileptic patients is related to geomagnetic activity we exposed rats in which limbic epilepsy had been induced to experimentally produced magnetic fields designed to simulate sudden storm commencements (SSCs). Prior studies with rats had shown that sudden death in groups of rats in which epilepsy had been induced months earlier was associated with the occurrence of SSCs and increased geomagnetic activity during the previous night. Schnabel et al. [(2000) Neurology 54:903-908] found no relationship between SUD in human patients and geomagnetic activity. A total of 96 rats were exposed to either 500, 50, 10-40 nT or sham (less than 10 nT) magnetic fields for 6 min every hour between midnight and 0800 hours (local time) for three successive nights. The shape of the complex, amplitude-modulated magnetic fields simulated the shape and structure of an average SSC. The rats were then seized with lithium and pilocarpine and the mortality was monitored. Whereas 10% of the rats that had been exposed to the sham field died within 24 h, 60% of the rats that had been exposed to the experimental magnetic fields simulating natural geomagnetic activity died (P<.001) during this period. These results suggest that correlational analyses between SUD in epileptic patients and increased geomagnetic activity can be simulated experimentally in epileptic rats and that potential mechanisms might be testable directly.

Animals↗

Suppression of experimental allergic encephalomyelitis in rats by 50-nT, 7-Hz amplitude-modulated nocturnal magnetic fields depends on when after inoculation the fields are applied.

Female Lewis rats (n = 88) were inoculated with an emulsion of spinal cord and complete Freund's adjuvant. They were then exposed in 11 separate blocks of experiments over a year period for approximately 6 min every hour between midnight and 08:00 h during post-inoculation nights 1-7, 8-16, 1-16, or 9 and 10 to 50-nT, 7-Hz, amplitude-modulated magnetic fields or to sham field (control) conditions. Compared to the control rats those exposed to the magnetic fields for nights 1-7 and nights 9-10 displayed more severe clinical symptoms while those exposed for nights 1-16 or 8-16 showed less severe symptoms. There was a strong correlation between the severity of the clinical symptoms in the control groups and the global geomagnetic activity 9 and 10 days after inoculation. These results suggest that the immunosuppressive effects of weak nocturnal magnetic fields may depend upon when they are applied during various stages in the development of a disease.

Animals↗

Thermal analgesia induced by 30-min exposure to 1 microT burst-firing magnetic fields is strongly enhanced in a dose-dependent manner by the alpha2 agonist clonidine in rats.

Most of the research concerning analgesia following brief exposures to physiologically patterned weak magnetic fields has focused upon their morphine-related properties. However, the alpha-adrenergic system interacts with morphine-induced analgesia. In the present study we found that prazosin, phenylephrine, and yohimbine did not augment the robust analgesia to thermal stimuli in rats evoked by whole-body exposures to a 1 microT, burst-firing magnetic field presented once every 4s for 30 min. However, the alpha2 agonist clonidine enhanced the field-induced analgesia in a dose-dependent manner that reflected a receptor-saturation response. Potentiation between the field and clonidine was evident at 0.2 mg/kg and approached asymptote at 1 mg/kg. The combination of the effects from exposure to the magnetic field and the clonidine explained more than 75% of the variance in the change in nociceptive thresholds from baseline levels. The possibility that properly patterned weak magnetic fields could be a powerful adjunct to pharmacological treatments of pain is considered.

Adrenergic alpha-2 Receptor Agonists↗

Normal spatial and contextual learning for ketamine-treated rats in the pilocarpine epilepsy model.

Cognitive impairments frequently accompany epileptic disorders. Here, we examine two neuroprotective agents, the noncompetitive NMDA antagonist ketamine and the dopaminergic antagonist acepromazine, for their efficacy in attenuating cognitive impairments in the lithium-pilocarpine (LI-PILO) model of rat limbic epilepsy. Declarative-like cognitive behaviors were assessed in a Morris water maze task that consisted successively of spatial and nonspatial (cued platform) training. Whereas the ketamine-treated (Ket) LI-PILO rats performed equally in all respects to nonseized control rats for the spatial and nonspatial components of the water maze task, the acepromazine-treated (Ace) LI-PILO rats failed to demonstrate learning in either the hidden or cued platform variants of the task and did not demonstrate any place learning in the platform-removed probe trials. We further assessed nondeclarative (associative) cognitive behaviors with a standard contextual fear-conditioning protocol. LI-PILO rats treated with acepromazine failed to learn the Pavlovian relationship; Ket LI-PILO rats performed equivalently to nonseized controls. Cumulatively, these data suggest robust cognitive sparing for LI-PILO rats with pharmacological NMDA receptor antagonism following induction of status epilepticus (SE). This cognitive sparing occurs despite earlier findings that the mean amount of total brain damage with LI-PILO is equivalent for Ket and Ace rats.

Animals↗

Thermal analgesic effects from weak, complex magnetic fields and pharmacological interactions.

In several experiments, robust analgesia (equivalent to about 4 mg/kg of morphine) in male rats to thermal stimuli following exposures to weak (1 microT) complex magnetic fields was explored. The analgesia occurred when patterns of magnetic fields with burst-firing-like configurations were presented for 30 min once every approximately 4 s. The analgesic effects were intensity dependent. A different frequency-modulated pattern produced analgesia more quickly. The analgesic effects following exposure to the burst-firing magnetic fields were augmented conspicuously by preinjections of morphine (4 mg/kg) or agmatine (10 mg/kg), but blocked by naloxone (1 mg/kg). The results of these experiments suggest that rational design of the temporal structure of weak magnetic fields may be a novel, inexpensive, and reliable technique for elevating thresholds to some classes of painful stimuli.

Analgesia↗

The neuromatrix and the epileptic brain: behavioral and learning preservation in limbic epileptic rats treated with ketamine but not acepromazine.

Conceiving the organization of the brain as a "neuromatrix" could provide significant insights into how different injuries to the nervous system could result in very distinct changes in behavior. The use of different pharmacological treatments to combat the deleterious consequences of such injuries is common practice. However, such treatments may have the capacity to alter the configurations of various neuronal circuits that contribute to the "neuromatrix" by selectively preventing damage to some pathways while facilitating the spread of destruction along others. The choice of pharmacological treatment may have profound consequences on the recovery of normal functioning following injury. We examined the behavior of rats treated with one of two potentially neuroprotective agents, the N-methyl-D-aspartate antagonist ketamine and the atypical neuroleptic acepromazine, on seizures induced by lithium-pilocarpine. Rats treated with ketamine following seizure onset were virtually indistinguishable from nonepileptic controls on a variety of behavioral tasks that included tests on learning, memory, and anxiety. In contrast, acepromazine-treated rats showed marked deficits on all learning and behavioral measures tested. These results suggest that administration of ketamine relatively soon after the emergence of epilepsy can prevent many of the cognitive deficits that are commonly found in rats subjected to lithium-pilocarpine-induced seizures. Further clinical testing investigating ketamine as a potential adjunct treatment for epilepsy may be well warranted.

Acepromazine↗

Emergence of spontaneous seizures during the year following lithium/pilocarpine-induced epilepsy and neuronal loss within the right temporal cortices.

Thirty days after the induction of seizures in 16 rats with lithium (3 mEq/kg) and pilocarpine (30 mg/kg), the numbers of episodes of motor seizures (rapid forelimb clonus) during daily 10-minute observational periods were recorded for 11 months. The proportions of neuronal loss were ranked using two methods by light microscopy for all structures between the posterior and anterior commissures. Amounts of damage within the dentate gyrus, hilus (CA4), and CA3 field were most strongly correlated with numbers of seizures per month about 6 months before the brains were removed. The strongest correlations occurred between the amounts of damage within the right temporal cortices, even after the variance associated with damage within the dentate gyrus had been removed, and the numbers of seizures during the last 2 months. These results may explain the greater proportion of spontaneous seizures that begin with left side forelimb clonus and suggest a particular sensitivity of the right side of the brain to either their initiation or their consequences.

Animals↗

Agility, gnosis, and graphaesthesia for the toes and fingers in children: normative data (ages 7-14 years).

The differential representation of the toes/feet and fingers/hands along the medial and lateral surfaces of the cerebral cortices, respectively, may have diagnostic utility. Normative data for errors for toe and finger graphaesthesia and gnosis, as well as foot and finger agility, were collected for 86 children (ages 7 to 14). The fingers were more agile than the feet, and the right side of the body was more agile than the left side, regardless of age. A marked improvement in toe gnosis, but not in finger gnosis occurred in children after 11-12 years of age. A statistically significant interaction between laterality and gender was due to the greater numbers of errors for both toe and finger gnosis, displayed by girls for the left sides of their bodies compared to their right sides. This discrepancy was not significant for boys.

Adolescent↗

Electrophysiological and quantitative electroencephalographic measurements after treatment by transcerebral magnetic fields generated by compact disc through a computer sound card: the Shakti treatment.

Quantitative electroencephalographic activity over the left and right frontal, temporal, parietal, and occipital lobes was obtained on 4 successive weeks in 12 subjects before they were exposed cerebrally for 30 min to one of two configurations of weak complex magnetic fields or to a sham-field condition. The two configurations were Shakti (c Todd Murphy) and the set of 4 solenoids (Koren boxes) generating a burst-firing magnetic field through the temporal lobes. Compared to baseline measurements there were no statistically significant differences in treatments for relative changes in power over these regions within the delta, theta, low alpha, beta, or gamma ranges. However within the high alpha range (10.5 Hz to 13 Hz), there was a significant interaction between session and type of treatment that was due primarily to the Shakti treatment. These changes were congruent with the subjective experiences reported by some users of the technology.

Adult↗

Lithium ion "cyclotron resonance" magnetic fields decrease seizure onset times in lithium-pilocarpine seized rats.

The cyclotron resonance equation predicts that the frequency of an applied magnetic field that might optimally interact with a single ion species may be computed as a function of the charge-to-mass ratio of the ion and the strength of the background static magnetic field. The present study was undertaken to discern the applicability of this equation for optimizing lithium ion utilization in the rat, as inferred by the predicted magnetic "ion resonance "field-induced shift of lithium's dose-dependent curve for seizure onset times (SOTs) when combined with the cholinergic agent pilocarpine. Groups of rats were administered 1.5 thru 3 mEq/kg lithium chloride (in 0.5 mEq/kg increments) and exposed to reference conditions or to one of three intensities (70 nanoTesla, 0.8 microTesla, or 25 microTesla) of a 85 Hz magnetic field calculated to resonate with lithium ions given the background static geomagnetic field of approximately 38,000 nanoTesla (0.38 Gauss). A statistically significant quadratic relationship for SOT as a function of magnetic field intensity (irrespective of lithium dose) was noted: this U-shaped function was characterized by equal SOTs for the reference and 25 microTesla groups, with a trend toward shorter SOTs for the 70 nanoTesla and 0.8 microTesla groups. Although not predicted by the equations, this report extends other findings suggestive of discrete intensity windows for which magnetic field frequencies derived from the cyclotron ion resonance equation may affect ion activity.

Analysis of Variance↗

Power increases within the gamma range over the frontal and occipital regions during acute exposures to cerebrally counterclockwise rotating magnetic fields with specific derivatives of change.

A total of 11 men and women were exposed for 5 min each to six different temporal configurations of pulsed magnetic fields that were delivered through serial activation of 8 solenoids in a counterclockwise direction around the head within the horizontal plane above the ears. Twenty-second samples of quantitative electroencephalographic activity within the delta, theta, lower alpha, upper alpha, beta, and gamma regions were collected after each configuration had been activated for 2.5 min. Only the circumcerebral presentation of the first pulse for 25 ms followed by an acceleration of +2 ms to each of the other 7 solenoids (the last duration = 11 ms) resulted in a significant increase in power within the gamma range (35 Hz to 45 Hz) over both frontal and occipital lobes but not over the parietal or temporal lobes. These results suggest topical application of specific spatial-temporal configurations of magnetic fields may affect the recursive creation of the rostral-caudal waves of cohesive fields that might produce consciousness.

Adult↗