ABSTRACT
Leptin has been shown to modulate gastrointestinal functions including nutrient absorption, growth, and inflammation and to display complex effects on gut motility. Leptin receptors have also been identified within the enteric nervous system (ENS), which plays a crucial role in digestive functions. Although leptin has recently been shown to activate neurons in the ENS, the precise mechanisms involved are so far unknown. Therefore, the aim of the present study was to determine the effects of leptin on rat proximal colon smooth muscle and enteric neuron activities. The effects of exogenous leptin on tone and on responses to transmural nerve stimulation (TNS) of isolated circular smooth muscle of proximal colon in rats were investigated using an organ bath technique. The effects of a physiological concentration (0.1 µM) of leptin were also studied on tone and TNS-induced relaxation in the presence of atropine, hexamethonium, L-N(G)-nitroarginine methyl ester (L-NAME) and capsazepine. Leptin caused a slight but significant decrease in tone, TNS-induced relaxation and contraction in a concentration-dependent manner in colonic preparations. Cholinergic antagonists abolished the effects of 0.1 µM leptin on TNS-induced relaxation. This concentration of leptin had no further effect on relaxation in the presence of L-NAME. In the presence of capsazepine, leptin had no further effect either on tone or relaxation compared to the drug alone. In conclusion, leptin modulates the activity of enteric inhibitory and excitatory neurons in proximal colon. These effects may be mediated through nitrergic neurons. Intrinsic primary afferent neurons may be involved.
Subject(s)
Colon/physiology , Leptin/physiology , Acetylcholine/pharmacology , Animals , Capsaicin/analogs & derivatives , Capsaicin/pharmacology , Cholinergic Agonists/pharmacology , Colon/drug effects , Colon/innervation , Enteric Nervous System/physiology , Hexamethonium/pharmacology , Humans , In Vitro Techniques , Leptin/pharmacology , Male , Muscle Contraction/drug effects , Muscle, Smooth/drug effects , Muscle, Smooth/metabolism , Muscle, Smooth/physiology , NG-Nitroarginine Methyl Ester/pharmacology , Nicotinic Antagonists/pharmacology , Nitric Oxide/physiology , Nitric Oxide Synthase/antagonists & inhibitors , Nitric Oxide Synthase/metabolism , Rats , Rats, Wistar , Synaptic TransmissionABSTRACT
OBJETIVO: Apresentar uma ferramenta de análise de dados que pode ser utilizada para proteção de pacientes e trabalhadores em áreas de uso de equipamentos móveis. MATERIAIS E MÉTODOS: Foi desenvolvida uma ferramenta, em planilha ativa Excel®, que utiliza medidas de exposição para gerar um banco de dados de fatores de forma e calcular o kerma no ar ao entorno de um leito. O banco de dados inicial foi coletado com três equipamentos móveis. Um espalhador não antropomórfico foi utilizado, sendo realizadas medidas de exposição em uma malha de (4,2 × 4,2) m², ao passo de 0,3 m. RESULTADOS: A ferramenta calcula o kerma no ar (associado à exposição de pacientes expostos e ao equivalente de dose ambiente) à radiação secundária. Para distâncias inferiores a 60,0 cm, valores acima do limite máximo de equivalente de dose ambiente definido para área livre (0,5 mSv/ano) foram verificados. Os dados coletados a 2,1 m foram sempre inferiores a 12% do referido limite. CONCLUSÃO: A ferramenta é capaz de auxiliar na proteção radiológica de pacientes e trabalhadores, quando associada à coleta de dados adequada, pois possibilita a determinação de áreas livres ao entorno de leitos em áreas onde equipamentos móveis geradores de radiação X são utilizados.
OBJECTIVE: To present a data analysis toolkit that may be utilized with the purpose of radiation protection of hospital inpatients and workers in areas where mobile apparatuses are used. MATERIALS AND METHODS: An Excel® ActiveSheet was utilized to develop a computational toolkit with exposure measurements to generate a database of shape factors and to calculate the air kerma around hospital beds. The initial database included data collected with three mobile apparatuses. A non-anthropomorphic phantom was utilized and exposure measurements were performed on a (4.2 × 4.2) m² mesh-grid at 0.3 m steps. RESULTS: The toolkit calculates the air kerma (associated with patients' radiation exposure and with ambient equivalent dose) under secondary radiation. For distances lower than 60.0 cm, values above the maximum ambient equivalent dose threshold defined for radiation free areas (0.5 mSv/year) were verified. Data collected at 2.1 m have always presented values lower than 12% of that threshold. CONCLUSION: The toolkit can aid in the radiological protection of patients and workers, provided it is combined with appropriate data collection, since it allows the determination of radiation free areas around beds in rooms where mobile X-ray apparatuses are utilized.
