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1.
Hum Exp Toxicol ; 40(1): 81-89, 2021 Jan.
Article in English | MEDLINE | ID: mdl-32748713

ABSTRACT

Exposure to paraquat is possibly involved with the development of several conditions, including neurodegenerative diseases, such as Parkinson's disease (PD). This condition is mainly characterized by the loss of dopaminergic neurons in the nigrostriatal pathway and the development of classical motor symptoms. Etiology includes exposure to environmental factors, such as the paraquat exposure, and inflammatory diseases may exacerbate paraquat neurotoxicity. The aim of the study was to investigate whether the exposure to paraquat associated with the presence of periodontal disease is able to induce motor and biochemical changes in rats similar to that observed in PD. Adult male Wistar rats were sent to ligature. After 48 h, they were sent to daily treatment paraquat (1 mg/kg/day; 2 mL/kg; intragastric) or vehicle for 4 weeks. Twenty-four hours after the last administration, the open field test was performed. The rats were euthanized and the left hemimandibles and striatum were dissected for the analysis of dopaminergic and inflammatory markers. Only the combination of periodontal disease model plus paraquat exposure induced motor impairments. Remarkably, the paraquat exposure increased the ligature-induced alveolar bone loss in hemimandibles. Moreover, only the combination of periodontal disease and paraquat exposure induced the loss of dopaminergic neurons and astrocyte activation in the striatum.


Subject(s)
Herbicides/toxicity , Motor Activity/drug effects , Paraquat/toxicity , Animals , Male , Periodontal Diseases , Rats , Rats, Wistar
2.
Transplant Proc ; 36(10): 3105-6, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15686706

ABSTRACT

Improvements in perioperative care, namely, organ preservation solutions, immunosuppression, and increased experience of surgical, anesthetic, and intensive care teams, have contributed to the success of pancreas transplantation. The objective of this study was to present data on anesthesia for pancreas transplantation alone (PTA) or simultaneous with kidney (SPKT), evaluating crystalloid, albumin and blood component infusions, graft ischemic times, and weights and ages of recipient. We evaluated patients undergoing SPKT (n=73), PTA (n=49), or SPKT with kidney living donor (n=8). Aggressive monitoring and therapy were used to avoid hypoperfusion, optimized with intravenous fluids, vasoative drugs, and correction of metabolic disturbances. Three SPKT patients were not extubated at the end of surgery. There were no other complications related to anesthesia in any patient. Although it is a high-risk surgery, PTA or SPKT is routine in our practice. Adequate perioperative care is important not only for the safety of the procedure but also for graft viability, contributing to a promising long-term treatment of insulin-dependent diabetic patients.


Subject(s)
Anesthesia/methods , Kidney Transplantation/methods , Pancreas Transplantation/methods , Adult , Humans , Living Donors , Monitoring, Intraoperative/methods , Treatment Outcome
3.
Behav Brain Res ; 124(1): 9-18, 2001 Sep 28.
Article in English | MEDLINE | ID: mdl-11423161

ABSTRACT

Intra-nigral administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyrindine (MPTP) caused a lesion in the substantia nigra, compact part (SNc) and a specific loss of dopamine and its metabolites in the striatum of rats. The animals were then tested in the two-way active avoidance task. MPTP-treated animals presented lower learning scores in the training and test sessions, an effect that was not caused by motor impairment or by a decreased sensitivity to footshock since their reaction time to the footshock (unconditioned stimulus - UCS) was not reduced. These lower scores were also not attributable to lower acoustic sensitivity or to a slowing in the association of the sound cue (conditioned stimulus - CS) with the UCS since the reaction time to the CS in the active avoidance response did not differ between MPTP-treated and control groups. Therefore, these results are more properly attributable to an impairment of the memory acquisition and retention processes. In addition, this study is presented as a model of early Parkinson's Disease amnesia and is discussed in terms of the importance of the nigrostriatal pathway to memory acquisition and storage processes.


Subject(s)
1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine , Avoidance Learning/drug effects , Mental Recall/drug effects , Parkinsonian Disorders/chemically induced , Substantia Nigra/drug effects , 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine/pharmacology , Animals , Association Learning/drug effects , Association Learning/physiology , Avoidance Learning/physiology , Conditioning, Classical/drug effects , Conditioning, Classical/physiology , Dopamine/metabolism , Male , Mental Recall/physiology , Neural Pathways/drug effects , Neural Pathways/physiopathology , Parkinsonian Disorders/physiopathology , Rats , Rats, Wistar , Retention, Psychology/drug effects , Retention, Psychology/physiology , Substantia Nigra/physiopathology
4.
Int J Neuropsychopharmacol ; 4(4): 361-70, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11806861

ABSTRACT

The objective of the present investigation was to test the effects of benserazide/L-dopa treatment in a model of learning and memory deficits associated with early Parkinson's disease. Intra-nigral administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) caused a lesion in the substantia nigra, compact part and a specific loss of dopamine (DA) and its metabolites in the striatum of rats and a memory impairment in the two-way active avoidance task. The administration of benserazide/L-dopa (50 and 200 mg/kg) to the MPTP-lesioned rats restored the striatal level of DA, but did not reverse the MPTP-induced learning and memory impairment. As this treatment caused a large increase of DA levels in extrastriatal brain regions of the MPTP-lesioned animals, this study suggests that benserazide/L-dopa therapy was not effective in improving the observed learning impairment because this treatment appears to tilt the balance between DA levels in the striatum and in the extrastriatal regions, such as frontal cortex and limbic structures, resulting in a cognitive deficit.


Subject(s)
1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine , Antiparkinson Agents/therapeutic use , Corpus Striatum/metabolism , Dopamine Agents , Dopamine/metabolism , Levodopa/therapeutic use , Memory Disorders/chemically induced , Memory Disorders/drug therapy , Animals , Avoidance Learning/drug effects , Benserazide/pharmacology , Biogenic Monoamines/metabolism , Brain Chemistry/drug effects , Corpus Striatum/drug effects , Corpus Striatum/pathology , Male , Memory Disorders/pathology , Rats , Rats, Wistar , Tyrosine 3-Monooxygenase/metabolism
5.
Arq Bras Cardiol ; 68(4): 245-8, 1997 Apr.
Article in Portuguese | MEDLINE | ID: mdl-9497504

ABSTRACT

PURPOSE: To analyse the main cardiac risk factors responsible for immediate and late outcomes in patients undergoing thoracic surgeries. METHODS: We performed a retrospective analysis of 90 cases of cardiac patients submitted to non-cardiac thoracic surgeries. Surgeries were divided into greater ones and others and the heart diseases into severe and mild disease. We analysed immediate and late complications, and the mortality inside these groups. RESULTS: We found a greater morbi-mortality in the greater surgeries group and a greater late mortality in the severe heart disease group. There were evidences that the degree of the heart disease does not influence immediate outcome. CONCLUSION: The heart disease was not a limiting immediate risk for surgery.


Subject(s)
Heart Diseases/complications , Intraoperative Complications/epidemiology , Postoperative Complications/epidemiology , Thoracic Surgical Procedures , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Retrospective Studies , Risk Factors
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