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Maternal deprivation, as a result of the artificial rearing (AR) paradigm, disturbs electrophysiological and histological characteristics of the peripheral sensory sural (SU) nerve of infant and adult male rats. Such changes are prevented by providing tactile or social stimulation during isolation. AR also affects the female rat's brain and behavior; however, it is unknown whether this early adverse experience also alters their SU nerve development or if tactile stimulation might prevent these possible developmental effects. To assess these possibilities, the electrophysiological and histological characteristics of the SU nerve from adult diestrus AR female rats that: (i) received no tactile stimulation (AR group), (ii) received tactile stimulation in the anogenital and body area (AR-Tactile group), or (iii) were mother reared (MR group) were determined. We found that the amplitude, but not the area, of the evoked compound action potential response in SU nerves of AR rats was lower than those of SU nerves of MR female rats. Tactile stimulation prevented these effects. Additionally, we found a reduction in the outer diameter and myelin thickness of axons, as well as a large proportion of axons with low myelin thickness in nerves of AR rats compared to the nerves of the MR and AR-Tactile groups of rats; however, tactile stimulation only partially prevented these effects. Our data indicate that maternal deprivation disturbs the development of sensory SU nerves in female rats, whereas tactile stimulation partially prevents the changes generated by AR. Considering that our previous studies have shown more severe effects of AR on male SU nerve development, we suggest that sex-associated factors may be involved in these processes.

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To investigate variations regarding the formation and course of the sural nerve (SN). We dissected 60 formalin-fixed Brazilian fetuses (n = 120 lower limbs) aged from the 16th to 34th weeks of gestational age. Three incisions were made in the leg to expose the SN, and the gastrocnemius muscle was retracted to investigate the SN course. Statistical analyses regarding laterality and sex were performed using the Chi-square test. Eight SN formation patterns were classified after analysis. Type 4 (in which the SN is formed by the union of the MSCN with the LSCN) was the most common SN formation pattern. Although there was no statistical association between the formation patterns and the lower limb laterality (p = 0.9725), there was as to sex (p = 0.03973), indicating an association between anatomical variation and sex. The site of branch joining was in the distal leg most time (53.75%). In all lower limbs, the SN or its branches crossed from the medial aspect of the leg to the lateral margin of the calcaneal tendon (CT). Most often, the SN is formed by joining the MSCN and the LSCN in the distal leg. The SN or its branches ran close to the saphenous vein, crossed the CT from medial to lateral, and distributed around the lateral malleolus.

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Demonstration of the possibility to obtain the sensory nerve action potential (SNAP) of sural nerve in patients over 60 years old, without peripheral neuropathy. Prospective study on 101 patients older than 60 years of age. Stimulation was applied 12 cm proximal to the recording point. Two hundred and two SNAPs of the sural nerve were collected with an average peak latency of 3.2 ms, onset latency of 2.6 ms, peak-to-peak amplitude of 15.2 µV and velocity of 45.7 m/s. It was possible to obtain the sural nerve SNAP in all tested patients older than 60, without peripheral neuropathy. The values obtained in this study prove to be useful as a reference in the evaluation of patients older than 60 years of age.

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Despite the frequent clinical hyper- or hypothermia cases, thermal-dependence of the endogenous pain modulation system at the spinal cord is not well understood. We evaluate spinal dorsal horn neuronal network responses during mechanical heterotopic noxious stimuli (HNS) at three different body temperatures (34; 37 or 40°C) by measuring lumbar cord dorsum potentials activated by electrical stimulation of the ipsilateral sural nerve in adult thiopental anesthetized rats. A noxious clamp was applied randomly to the tail, right hindpaw, right forepaw, muzzle and left forepaw. HNS induced a decrease of the N wave amplitude and duration at 37°C. This effect was reduced at 40°C for both amplitude (-18.2% for 37-40°C; P<0.0005) and duration (-16.4% for 37-40°C; P<0.0001). P wave did not show neither amplitude nor duration changes at neither 3 tested temperatures. Clinical range changes of temperature could modify pain sensation, moreover, hyperthermia increases nociceptive sensory input to dorsal horn, and could exacerbate pain sensation in individuals with fever.

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Most of the endogenous pain modulation (EPM) involves the spinal dorsal horn (SDH). EPM including diffuse noxious inhibitory controls have been extensively described in oligoneuronal electrophysiological recordings but less attention had been paid to responses of the SDH neuronal population to heterotopic noxious stimulation (HNS). Spinal somatosensory-evoked potentials (SEP) offer the possibility to evaluate the neuronal network behavior, reflecting the incoming afferent volleys along the entry root, SDH interneuron activities and the primary afferent depolarization. SEP from de lumbar cord dorsum were evaluated during mechanical heterotopic noxious stimuli. Sprague-Dawley rats (n = 12) were Laminectomized (T10-L3). The sural nerve of the left hind paw was electrically stimulated (5 mA, 0.5 ms, 0.05 Hz) to induce lumbar SEP. The HNS (mechanic clamp) was applied sequentially to the tail, right hind paw, right forepaw, muzzle and left forepaw during sural stimulation. N wave amplitude decreases (-16.6 %) compared to control conditions when HNS was applied to all areas of stimulation. This effect was more intense for muzzle stimulation (-23.5 %). N wave duration also decreased by -23.6 %. HNS did not change neither the amplitude nor the duration of the P wave but dramatically increases the dispersion of these two parameters. The results of the present study strongly suggest that a HNS applied to different parts of the body is able to reduce the integrated electrical response of the SDH, suggesting that not only wide dynamic range neurons but many others in the SDH are modulated by the EPM.

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OBJECTIVE: Establishing reference values for neuroconduction studies regarding the peroneal, tibial and sural nerves in a group of young adults. MATERIALS AND METHODS: Neuroconduction was tested (also known as nerve conduction velocity (NCV) tests) on 155 asymptomatic subjects' tibial, peroneal and sural nerves using current conventional techniques, after informed written consent had been obtained. Reference values were obtained and presented as averages, standard deviations and percentiles, along with their correlation with parameters such as age, weight and height, via bivariate analysis of linear correlation using Spearman's rank correlation test. RESULTS: Peroneal nerve average distal latency was 3.6 ms (0.4 SD), amplitude 6.1 mV (2.0 SD) and conduction velocity 54.8m/s (4.2 SD). Average tibial nerve distal latency was 3.5 ms (0.4 SD), amplitude 16.7mV (4.7 SD) and conduction velocity 53 m/s (3.8 SD). Average sural nerve peak latency was 3.4 ms (0.3 SD) and amplitude 21.3V (5.0 SD). Peroneal and tibial nerve upper limit of normal side to side variation was 0.8ms (average+2DE) and 0.4 ms (average + 2 SD) for the sural nerve. A statistically significant relationship was found with variables such as weight, height and age. CONCLUSIONS: The values so obtained could be used in Colombia's electrophysiology laboratories as reference in evaluating patients' suffering musculoskeletal pathologies and different types of polyneuropathy.

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OBJECTIVE: To assess whether sensorimotor peripheral nerve function is associated with muscle power in community-dwelling older men. DESIGN: Longitudinal cohort study with 2.3±0.3 years of follow-up. SETTING: One clinical site. PARTICIPANTS: Participants (n=372; mean age ± SD, 77.2±5.1y; 99.5% white; body mass index, 27.9±3.7kg/m(2); power, 1.88±0.6W/kg) at 1 site of the Osteoporotic Fractures in Men Study (N=5994). INTERVENTIONS: Not applicable. MAIN OUTCOME MEASURES: A nerve function ancillary study was performed 4.6±0.4 years after baseline. Muscle power was measured using a power rig. Peroneal motor nerve conduction amplitude, distal motor latency, and mean f-wave latency were measured. Sensory nerve function was assessed using 10-g and 1.4-g monofilaments and sural sensory nerve conduction amplitude and distal latency. Peripheral neuropathy symptoms at the leg and feet were assessed by self-report. RESULTS: After adjustments for age, height, and total body lean and fat mass, 1 SD lower motor (ß=-.07, P<.05) and sensory amplitude (ß=-.09, P<.05) and 1.4-g (ß=-.11, P<.05) and 10-g monofilament insensitivity (ß=-.17, P<.05) were associated with lower muscle power/kg. Compared with the effect of age on muscle power (ß per year, -.05; P<.001), this was equivalent to aging 1.4 years for motor amplitude, 1.8 years for sensory amplitude, 2.2 years for 1.4-g monofilament detection, and 3.4 years for 10-g detection. Baseline 1.4-g monofilament detection predicted a greater decline in muscle power/kg. Short-term change in nerve function was not associated with concurrent short-term change in muscle power/kg. CONCLUSIONS: Worse sensory and motor nerve function were associated with lower muscle power/kg and are likely important for impaired muscle function in older men. Monofilament sensitivity was associated with a greater decline in muscle power/kg, and screening may identify an early risk for muscle function decline in late life, which has implications for disability.

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The aim of this study was to determine the effect of chronic undernourishment on the amplitude depression of the first negative component in the cord dorsum potentials (N(1)-CDPs) caused by the conditioning stimulation of sensory cutaneous nerves in the rat spinal cord. Single electrical pulses (1Hz; 2 times threshold) applied to the sural (SU) nerve of control rats (n=14) produced CDPs with a first negative component (N(1)-CDPs) larger in amplitude (14.2±1.3%, p<0.01) than those recorded in chronically undernourished rats (n=14; 3 times threshold). The conditioning stimulation of the SP nerve (4 shocks at 300Hz, 3×T) in the control rats (n=5) evoked a long-lasting (~200ms) depression of the N(1)-CDP (60.2±7.2%). In contrast such depression was smaller in magnitude (42.5±5.7%, p<0.01) and time course (100-120ms) in undernourished rats (n=7). The systemic application of picrotoxin (PTX) reduced, but did not abolish the conditioned depression of the N(1)-CDPs and DRPs in both the control and undernourished rats. By assuming that the depression of the N(1)-CDPs is representative of presynaptic mechanisms, it is proposed that chronic undernourishment influence the activation of presynaptic neuronal pathways that regulate the transmitter release of cutaneous afferent fibers in the spinal cord and such effect could act as a compensatory mechanism that counterbalances the decreased activation of spinal neurons by the reduced afferent input in the rat.

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Pain is a subjective and individual sensation causing major discomfort. So, it is necessary to put into practice methods to objectively quantify it. Several studies indicate that evoked potentials (EP) generate responses which may reflect painful processes. This study reports the results of the application of two different protocols by using biopotentials to objectively measure pain. The first (protocol 1) evaluates the relation between pain, induced by electrical stimulation, and subjective perception and also with nociceptive flexion reflex (NFR) represented by muscle activity (electromyography) detected on the femoral biceps after sural nerve stimulation. The second protocol (protocol 2) verifies whether there is some correlation between M-wave parameters and subjective pain sensation. The results obtained from protocol 1 suggest that the area of the EMG envelope and entropy estimated from the EMG activity are correlated with subjective sensation of pain. The analysis of data obtained from protocol 2 shows a correlation between the global minimum of the M-wave and pain increase. These results contribute to studies which seek to objective measures for pain quantification based on the analysis of biopotentials.

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Objetivo Establecer valores de referencia de los estudios de neuroconducción de los nervios peroneo, tibial y sural en un grupo de adultos jóvenes. Materiales y Métodos Se realizaron neuroconducciones en 155 sujetos asintomáticos, de los nervios tibial, peroneo y sural, usando técnicas convencionales actuales y previo consentimiento informado. Se obtuvieron valores de referencia presentados con promedios, desviaciones estándar, percentiles y su correlación con parámetros como edad, peso y estatura a través de un análisis bivariado de correlación lineal utilizando la prueba de Spearman. Resultados Para el nervio peroneo el promedio de la latencia distal fue de 3,6ms (DE 0,4), la amplitud fue de 6,1mV (DE 2,0) y la velocidad de conducción 54,8m/s (DE 4,2). Para el nervio tibial el promedio de la latencia distal fue de 3,5ms (DE 0,4), la amplitud fue de 16,7mV (DE 4,7) y la velocidad de conducción 53m/s (DE 3,8). Para el nervio sural el promedio de la latencia al pico fue de 3,4ms (DE 0,3), la amplitud fue de 21,3mV (DE 5,0). El límite superior de la variación normal de la latencia lado a lado para el nervio peroneo y tibial fue de 0,8ms (promedio + 2DE) y para el nervio sural fue de 0,4ms (promedio + 2DE). Se encontró relación estadísticamente significativa con variables como peso, estatura y edad. Conclusiones Los valores obtenidos pueden ser utilizados en los laboratorios de electrofisiología de nuestro país como referencia en la evaluación de pacientes con patologías musculoesqueléticas y con diferentes tipos de polineuropatía.

Objective Establishing reference values for neuroconduction studies regarding the peroneal, tibial and sural nerves in a group of young adults. Materials and Methods Neuroconduction was tested (also known as nerve conduction velocity (NCV) tests) on 155 asymptomatic subjects' tibial, peroneal and sural nerves using current conventional techniques, after informed written consent had been obtained. Reference values were obtained and presented as averages, standard deviations and percentiles, along with their correlation with parameters such as age, weight and height, via bivariate analysis of linear correlation using Spearman's rank correlation test. Results Peroneal nerve average distal latency was 3.6ms (0.4 SD), amplitude 6.1mV (2.0 SD) and conduction velocity 54.8m/s (4.2 SD). Average tibial nerve distal latency was 3.5ms (0.4 SD), amplitude 16.7mV (4.7 SD) and conduction velocity 53m/s (3.8 SD). Average sural nerve peak latency was 3.4ms (0.3 SD) and amplitude 21.3V (5.0 SD). Peroneal and tibial nerve upper limit of normal side to side variation was 0.8ms (average+2DE) and 0.4ms (average + 2 SD) for the sural nerve. A statistically significant relationship was found with variables such as weight, height and age. Conclusions The values so obtained could be used in Colombia's electrophysiology laboratories as reference in evaluating patients' suffering musculoskeletal pathologies and different types of polyneuropathy.

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