Publicação
Comparative study on the physiological dynamics evoked by different profiles of lead exposure
| Resumo: | Lead is a toxic metal which widespread use has resulted in environmental contamination and significant health problems. It is a cumulative toxicant that affects multiple body systems, including the cardiovascular, hematopoietic, reproductive, and renal systems. Lead is also a well-known neurotoxin, inducing changes in neurogenesis, neurodegeneration and changes on glial cells. These changes in the molecular and cellular processes lead to cognitive and behaviour alterations, particularly during developmental phases, persisting throughout the lifetime. Most of the studies that have been performed in both humans and animals were focused in a continuous chronic exposure to lead. This lead exposure causes behavioural changes, cognitive impairment and hypertension associated with sympathoexcitation, baroreceptor reflex hyposensitivity and increased chemoreceptor reflex sensitivity. But the effects of an intermittent lead exposure are scarse and standardized animal models are non-existent. This pattern of exposure has been increasing in the last years due to migrations, implementation of school exchange programs and/or residential changes. Therefore, the overall purpose of this work was to evaluate lead effects on mammal’s physiology along different profiles of lead exposure, including a new animal model of intermittent low-level lead exposure. Animal models of lead exposure were developed by replacing the tap water of seven-day pregnant Wistar females with 0.2% (p/v) solution of lead acetate. After being weaned at 21 days, rat pups, both sexes, were divided into 3 groups of lead exposure: long-term (exposure from foetal period until 28 weeks of age), short-term (exposure from foetal period until 12 weeks) and intermittent (exposure from foetal period until 12 weeks, lead-free period until 20 weeks and a second exposure between 20 and 28 weeks of age). At 12, 20 and 28 weeks of age, behavioural tests were performed for anxiety (Elevated Plus Maze Test), locomotor activity (Open Field Test), spatial working memory (Y-Maze) and episodic long-term memory (Novel Object Recognition test) assessment. Blood pressure (BP), electrocardiogram (ECG), heart rate (HR) and respiratory frequency (RF) were recorded at the same timepoints in the acute experiment. Baroreflex gain (BRG), chemoreflex sensitivity (ChS), cardiovascular variability were also evaluated. Immunohistochemistry studies for neuronal nuclear antigen (NeuN), Synaptophysin (Syn), ionized calcium binding adapter molecule-1 (Iba-1) and Glial fibrillary acidic protein (GFAP) stainings were performed in brain slices, and confocal imaging acquired and stainings quantified at dentate gyrus (DG) of the hippocampus. Blood lead levels were assessed by atomic absorption spectroscopy and metabolic evaluation of all groups was done using metabolic cages. A control group of Wistar rats without lead exposure, of both sexes, with the same number of individuals, underwent the same protocol and were evaluated in the same time points. Student T-test and one-way ANOVA with Tukey’s multiple comparison between means were used (significance p<0.05) for statistical analysis. Our data showed a clear association between lead exposure, hypertension and cardiorespiratory reflexes impairment, without heart rate changes, independently of the type of lead exposure profile. We also demonstrated for the first time that lead intermittent exposure causes adverse health effects, i.e, hypertension, sympathetic overactivity, increased chemoreflex sensitivity and baroreflex impairment, similar to a chronic exposure, however less pronounced. In fact, at 28 weeks, PbI group, the intermittent animal model of lead exposure developed, had a less severe hypertension when compared to the long-term exposure group (PbP), which might suggest that the duration of Pb exposure is more relevant than the time of exposure. Moreover, the effect on diastolic blood pressure produced by lead exposure was more evident than that of systolic blood pressure. Lead exposure from foetal period until 12 weeks of age causes long lasting hypertension and chemoreceptor reflex dysfunction even after a 16 weeks period without exposure. However, the clearance of lead promoted an improvement in baroreceptor reflex function, with repercussions on blood pressure values, since these values decreased, but did not reached the normotensive values. Regarding the autonomic data, in our study, the overactivity of the sympathetic nervous system, evaluated by the LF band, is concomitant with baroreceptor reflex impairment and/or hypertension. This means that the sympathetic nervous system may be involved in the modulation of the baroreceptor reflexes responses or in the hypertension development due to lead exposure. Concerning the effect of lead at behavioural level, all groups exposed to lead, evaluated in the three different time points, had behavioural changes, namely anxiety, hyperactivity and/or long-term memory impairment and molecular changes in the hippocampus region, more specifically, reactive astrogliosis and microgliosis were detected, indicating the presence of neuroinflammation. However, these alterations seem to reverse after lead abstinence for a certain period (single exposure) and are enhanced when a second exposure occurs (intermittent exposure), along with a synaptic loss. In summary, this study shows, that exposure to lead during the developmental phase can alter the normal course of development, with lifelong health consequences. Since all exposed Pb groups had the same route of exposure (i.e. exposure to lead by water) and the same dose and, despite the different time of exposure, all were exposed to lead since foetal period until adulthood, the most susceptible period to adverse health effects. Therefore, we can conclude that the different effects of lead toxicant between groups mainly depends on the total duration of lead exposure. This comparative study brings new insights on the environmental factors that influence nervous and cardiovascular systems during development, which can help creating public policy strategies to prevent and control the adverse effects of Pb toxicity. |
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| Autores principais: | Shvachiy, Liana |
| Assunto: | Lead toxicity Autonomic dysfunction Hypertension Behavioural and cognitive changes Gliosis Teses de mestrado - 2018 |
| Ano: | 2018 |
| País: | Portugal |
| Tipo de documento: | dissertação de mestrado |
| Tipo de acesso: | acesso aberto |
| Instituição associada: | Universidade de Lisboa |
| Idioma: | inglês |
| Origem: | Repositório da Universidade de Lisboa |
| Resumo: | Lead is a toxic metal which widespread use has resulted in environmental contamination and significant health problems. It is a cumulative toxicant that affects multiple body systems, including the cardiovascular, hematopoietic, reproductive, and renal systems. Lead is also a well-known neurotoxin, inducing changes in neurogenesis, neurodegeneration and changes on glial cells. These changes in the molecular and cellular processes lead to cognitive and behaviour alterations, particularly during developmental phases, persisting throughout the lifetime. Most of the studies that have been performed in both humans and animals were focused in a continuous chronic exposure to lead. This lead exposure causes behavioural changes, cognitive impairment and hypertension associated with sympathoexcitation, baroreceptor reflex hyposensitivity and increased chemoreceptor reflex sensitivity. But the effects of an intermittent lead exposure are scarse and standardized animal models are non-existent. This pattern of exposure has been increasing in the last years due to migrations, implementation of school exchange programs and/or residential changes. Therefore, the overall purpose of this work was to evaluate lead effects on mammal’s physiology along different profiles of lead exposure, including a new animal model of intermittent low-level lead exposure. Animal models of lead exposure were developed by replacing the tap water of seven-day pregnant Wistar females with 0.2% (p/v) solution of lead acetate. After being weaned at 21 days, rat pups, both sexes, were divided into 3 groups of lead exposure: long-term (exposure from foetal period until 28 weeks of age), short-term (exposure from foetal period until 12 weeks) and intermittent (exposure from foetal period until 12 weeks, lead-free period until 20 weeks and a second exposure between 20 and 28 weeks of age). At 12, 20 and 28 weeks of age, behavioural tests were performed for anxiety (Elevated Plus Maze Test), locomotor activity (Open Field Test), spatial working memory (Y-Maze) and episodic long-term memory (Novel Object Recognition test) assessment. Blood pressure (BP), electrocardiogram (ECG), heart rate (HR) and respiratory frequency (RF) were recorded at the same timepoints in the acute experiment. Baroreflex gain (BRG), chemoreflex sensitivity (ChS), cardiovascular variability were also evaluated. Immunohistochemistry studies for neuronal nuclear antigen (NeuN), Synaptophysin (Syn), ionized calcium binding adapter molecule-1 (Iba-1) and Glial fibrillary acidic protein (GFAP) stainings were performed in brain slices, and confocal imaging acquired and stainings quantified at dentate gyrus (DG) of the hippocampus. Blood lead levels were assessed by atomic absorption spectroscopy and metabolic evaluation of all groups was done using metabolic cages. A control group of Wistar rats without lead exposure, of both sexes, with the same number of individuals, underwent the same protocol and were evaluated in the same time points. Student T-test and one-way ANOVA with Tukey’s multiple comparison between means were used (significance p<0.05) for statistical analysis. Our data showed a clear association between lead exposure, hypertension and cardiorespiratory reflexes impairment, without heart rate changes, independently of the type of lead exposure profile. We also demonstrated for the first time that lead intermittent exposure causes adverse health effects, i.e, hypertension, sympathetic overactivity, increased chemoreflex sensitivity and baroreflex impairment, similar to a chronic exposure, however less pronounced. In fact, at 28 weeks, PbI group, the intermittent animal model of lead exposure developed, had a less severe hypertension when compared to the long-term exposure group (PbP), which might suggest that the duration of Pb exposure is more relevant than the time of exposure. Moreover, the effect on diastolic blood pressure produced by lead exposure was more evident than that of systolic blood pressure. Lead exposure from foetal period until 12 weeks of age causes long lasting hypertension and chemoreceptor reflex dysfunction even after a 16 weeks period without exposure. However, the clearance of lead promoted an improvement in baroreceptor reflex function, with repercussions on blood pressure values, since these values decreased, but did not reached the normotensive values. Regarding the autonomic data, in our study, the overactivity of the sympathetic nervous system, evaluated by the LF band, is concomitant with baroreceptor reflex impairment and/or hypertension. This means that the sympathetic nervous system may be involved in the modulation of the baroreceptor reflexes responses or in the hypertension development due to lead exposure. Concerning the effect of lead at behavioural level, all groups exposed to lead, evaluated in the three different time points, had behavioural changes, namely anxiety, hyperactivity and/or long-term memory impairment and molecular changes in the hippocampus region, more specifically, reactive astrogliosis and microgliosis were detected, indicating the presence of neuroinflammation. However, these alterations seem to reverse after lead abstinence for a certain period (single exposure) and are enhanced when a second exposure occurs (intermittent exposure), along with a synaptic loss. In summary, this study shows, that exposure to lead during the developmental phase can alter the normal course of development, with lifelong health consequences. Since all exposed Pb groups had the same route of exposure (i.e. exposure to lead by water) and the same dose and, despite the different time of exposure, all were exposed to lead since foetal period until adulthood, the most susceptible period to adverse health effects. Therefore, we can conclude that the different effects of lead toxicant between groups mainly depends on the total duration of lead exposure. This comparative study brings new insights on the environmental factors that influence nervous and cardiovascular systems during development, which can help creating public policy strategies to prevent and control the adverse effects of Pb toxicity. |
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