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1.
Acta cir. bras ; 32(5): 396-406, May 2017. tab, graf
Article Dans Anglais | LILACS | ID: biblio-837708

Résumé

Abstract Purpose: To determine the effects of propofol and ketamine anesthesia on liver regeneration in rats after partial hepatectomy (PHT). Methods: Male Wistar albino rats were assigned randomly to four groups of 10. Anesthesia was induced and maintained with propofol in groups 1 and 2, and with ketamine in groups 3 and 4. PHT was undertaken in groups 1 and 3. Rats in groups 2 and 4 (control groups) underwent an identical surgical procedure, but without PHT. At postoperative day-5, rats were killed. Regenerated liver was removed, weighed, and evaluated (by immunohistochemical means) for expression of inducible nitric oxide synthase (iNOS), endothelial NOS (eNOS), apoptosis protease-activating factor (APAF)-1, and proliferating cell nuclear antigen (PCNA). Also, blood samples were collected for measurement of levels of tumor necrosis factor (TNF)-α and interleukin (IL)-6. Results: Between groups 2 and 4, there were no differences in tissue levels of iNOS, eNOS, and APAF-1 or plasma levels of TNF-α and IL-6. eNOS expression was similar in group 1 and group 3. Expression of iNOS and APAF-1 was mild-to-moderate in group 1, but significantly higher in group 3. Groups 1 and 3 showed an increase in PCNA expression, but expression in both groups was comparable. Plasma levels of TNF-α and IL-6 increased to a lesser degree in group 1 than in group 3. Conclusion: Propofol, as an anesthetic agent, may attenuate cytokine-mediated upregulation of iNOS expression and apoptosis in an animal model of liver regeneration after partial hepatectomy.


Sujets)
Animaux , Mâle , Propofol/pharmacologie , Apoptose , Anesthésiques intraveineux/pharmacologie , Nitric oxide synthase type II/métabolisme , Kétamine/pharmacologie , Régénération hépatique/effets des médicaments et des substances chimiques , Répartition aléatoire , Propofol/métabolisme , Régulation positive , Interleukine-6/métabolisme , Interleukine-6/sang , Rat Wistar , Antigène nucléaire de prolifération cellulaire/métabolisme , Anesthésiques intraveineux/métabolisme , Modèles animaux , Nitric oxide synthase type III/métabolisme , Facteur-1 activateur des protéases apoptotiques/métabolisme , Hépatectomie , Kétamine/métabolisme
3.
Journal of Forensic Medicine ; (6): 346-349, 2014.
Article Dans Chinois | WPRIM | ID: wpr-983928

Résumé

OBJECTIVE@#To select specific DNA aptamer for determining ketamine by FluMag-SELEX.@*METHODS@#Based on magnetic beads with tosyl surface modification as solid carrier and ketamine as target, a random ssDNA library with total length of 78 bp in vitro was compounded. After 13 rounds screening, DNA cloning and sequencing were done. Primary and secondary, structures were analyzed. The affinity, specificity and Kd values of selected aptamer were measured by monitoring the fluorescence intensity.@*RESULTS@#Two ssDNA aptamers (Apt#4 and Apt#8) were successfully selected with high and specific abilities to bind ketamine as target with Kd value of 0.59 and 0.66 μmol/L. The prediction of secondary structure was main stem-loop and G-tetramer. The stem was the basis of stability of aptamer's structure. And loop and G-tetramer was the key of specific binding of ketamine.@*CONCLUSION@#FluMag-SELEX can greatly improve the selection efficiency of the aptamer, obtain the ketamine-binding DNA aptamer, and develop a new method for rapid detection of ketamine.


Sujets)
Aptamères nucléotidiques/métabolisme , ADN , ADN simple brin/génétique , Techniques in vitro , Kétamine/métabolisme , Oligonucléotides , Technique SELEX/méthodes
4.
Pesqui. vet. bras ; 29(12): 969-973, Dec. 2009. ilus
Article Dans Portugais | LILACS | ID: lil-539129

Résumé

O estudo objetivou verificar a influência da temperatura corporal nos parâmetros fisiológicos e nos períodos de indução e recuperação anestésicos de cascavéis (Crotalus durissus) anestesiadas com cetamina. Os animais foram previamente submetidos à hipotermia (HIPO) (<22ºC) e normotermia (30ºC) (NORMO) e anestesiados com 80mg/kg IM de cetamina. Foram avaliados os períodos de latência e recuperação da anestesia por meio do tônus de cabeça, tônus muscular e reflexo de endireitamento. Mensurou-se a frequência cardíaca (FC), tempo de apnéia e temperatura corporal em 0 min e 5, 10, 15, 30, 60, 90, 120 min e análise dos gases sanguíneos em 0 min, 30 e 60 min. Não houve diferença em relação ao período de latência entre os grupos. A recuperação dos animais em HIPO foi mais prolongada (5,5 horas) que em NORMO (3,5 horas). Obteve-se FC no grupo NORMO superior que no grupo HIPO. O tempo de apnéia manteve o mesmo padrão em ambos os grupos. Em relação ao basal, tanto em HIPO quanto em NORMO o tempo de apnéia diminuiu acentuadamente entre 5 e 30 min. Observou-se acidose respiratória no grupo NORMO apenas em 0 min. O SvO2 elevou-se significativamente após 30 min, o mesmo ocorrendo com a PvO2. A PvCO2 diminuiu em ambos os grupos após 30 min. Evidenciou-se que a temperatura corporal influencia intrinsecamente o período de recuperação de cascavéis anestesiadas com cetamina.


The aim of the study was to verify the influence of the body temperature under physiological values and latency and recovery times on rattlesnakes anesthetized with ketamine. The animals were previously submitted to hypothermia (HYPO) (<22ºC) and normothermia (30ºC) (NORMO) and then, anesthetized with 80 mg/kg IM of ketamine. Latency and recovery times were evaluated by head tonus, muscular tonus and righting reflex. Heart rate (HR), time of apnea and body temperature were measured before and 5, 10, 15, 30, 60, 90 and 120 minutes after ketamine administration. Blood gases parameters were measured before, 30 and 60 minutes. It was not observed difference on latency time in both groups. The recovery time was higher on HYPO (5,5 hours) compared to NORMO (3,5 hours). HR was higher on NORMO compared to HYPO. Time of apnea was the same pattern on both groups. Compared to basal levels, time of apnea was shorter between 5 to 30 min on both groups. Respiratory acidosis was observed only at 0 min in NORMO. SvO2 was higher after 30 min, the same as with PvO2 in both groups. PvCO2 reduced after 30 min in both groups. It was evident that body temperature exerts intense influence on the recovery time on rattlesnakes anesthetized with ketamine.


Sujets)
Animaux , Réveil anesthésique , Température du corps , Kétamine/métabolisme , Crotalus/métabolisme
5.
Journal of Korean Medical Science ; : 113-120, 2005.
Article Dans Anglais | WPRIM | ID: wpr-110310

Résumé

Apoptosis is a programmed, physiologic mode of cell death that plays an important role in tissue homeostasis. As for the central nervous system, ischemic insults can induce pathophysiologic cascade of apoptosis in neurophils. Impairment of astroctye functions during brain ischemia can critically influence neuron survival by neuronglia interactions. We aimed to elucidate the protective effect of ketamine on apoptosis by energy deprivation in astrocytes. Ischemic insults was induced with iodoacetate/ carbonylcyanide mchlorophenylhydrazone (IAA/CCCP) 1.5 mM/ 20 micrometer or 150 micrometer/2 micrometer for 1 hr in the HTB-15 and CRL-1690 astrocytoma cells. Then these cells were reperfused with normal media or ketamine (0.1 mM) containing media for 1 hr or 24 hr. FITC-annexin-V staining and propidium iodide binding were determined by using flow cytometry. Cell size and granularity were measured by forward and side light scattering properties of flow cytometry system, respectively. An addition of keta-mine during reperfusion increased the proportion of viable cells. Ketamine alleviated cell shrinkage and increased granularity during the early period, and ameliorated cell swelling during the late reperfusion period. Ketamine may have a valuable effect on amelioration of early and late apoptosis in the astrocytoma cells, even though the exact mechanism remains to be verified.


Sujets)
Humains , Anesthésiques dissociatifs/pharmacologie , Annexine A5/pharmacologie , Apoptose , Astrocytes/métabolisme , Astrocytome/traitement médicamenteux , Encéphale/anatomopathologie , [(3-Chlorophényl)hydrazono]malononitrile/pharmacologie , Lignée cellulaire tumorale , Taille de la cellule , Survie cellulaire , Système nerveux central/effets des médicaments et des substances chimiques , Antienzymes/pharmacologie , Cytométrie en flux/méthodes , Indicateurs et réactifs/pharmacologie , Iodo-acétates/pharmacologie , Ischémie/anatomopathologie , Kétamine/métabolisme , Lumière , Neurones/métabolisme , Granulocytes neutrophiles/métabolisme , Perfusion , Propidium/pharmacologie , Diffusion de rayonnements , Facteurs temps , Agents découplants/pharmacologie
6.
Journal of Forensic Medicine ; (6): S5-7, 2005.
Article Dans Chinois | WPRIM | ID: wpr-983096

Résumé

The abuse of ketamine has gained popularity in recent years. It is important to develop rapid and accurate methods to determine ketamine and its metabolites in biological samples. The metabolites of ketamine are norketamine and dehydronorketamine in vivo. At present, there are blood, urine, hair and so on as specimens for detection, while the methods include GC, GC/MS, HPLC, LC/MS, HPCE etc. In this paper, these methods used for ketamine and its metabolites were reviewed in order to provide some preference for the study in relative fields.


Sujets)
Humains , Anesthésiques dissociatifs/composition chimique , Chromatographie en phase liquide à haute performance/méthodes , Médecine légale , Chromatographie gazeuse-spectrométrie de masse/méthodes , Poils/composition chimique , Kétamine/métabolisme , Sensibilité et spécificité , Détection d'abus de substances/méthodes
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