Influence of chlorpromazine on renal histology of rats submitted to ischemia and reperfusion injury

ABSTRACT PURPOSE: To analyze the influence of chlorpromazine on renal histology of rats submitted to ischemia and reperfusion injury. METHODS: Sixteen Wistar rats - split in two groups - have been used: control group, receiving 3 mg/kg isotonic saline solution through caudal vein, and, the chlorpromazine group, receiving 3 mg/kg-IV of such medication. The nephrectomy of the left kidney lower third was carried out; immediately, the test-drug was administrated. After 15 minutes of test-drug administration, the renal pedicle was clamped; in 60 minutes of ischemia it was released. After 24 hours of the renal reperfusion, the rats were, once more, anesthetized and submitted to total left nephrectomy, and, afterwards, to euthanasia. Histological findings regarding ischemia have been evaluated and compared between the groups. RESULTS: There was no statistical difference related to inferior renal pole histological analysis. Regarding 60-minute renal ischemia, chlorpromazine has statistically reduced the accrual of leucocytes within the vasa recta renis (p=0.036) and the congestion of peritubular capillaries (p=0.041). When conducting joint analysis of histological patterns, the control group showed a median score of 11 and chlorpromazine group of 5.5 (p=0.036). CONCLUSION: Chlorpromazine significantly reduced the occurrence of secondary damage to ischemia and reperfusion process in the overall histological analysis.

Muscular performance characterization in athletes: a new perspective on isokinetic variables

Background: Isokinetic dynamometry allows the measurement of several variables related to muscular performance, many of which are seldom used, while others are redundantly applied to the characterization of muscle function. Objectives: The present study aimed to establish the particular features of muscle function that are captured by the variables currently included in isokinetic assessment and to determine which variables best represent these features in order to achieve a more objective interpretation of muscular performance. Method: This study included 235 male athletes. They performed isokinetic tests of concentric knee flexion and extension of the dominant leg at a velocity of 60º/s. An exploratory factor analysis was performed. Results: The findings demonstrated that isokinetic variables can characterize more than muscle torque production and pointed to the presence of 5 factors that enabled the characterization of muscular performance according to 5 different domains or constructs. Conclusions: The constructs can be described by torque generation capacity; variation of the torque generation capacity along repetitions; movement deceleration capacity; mechanical/physiological factors of torque generation; and acceleration capacity (torque development). Fewer than eight out of sixteen variables are enough to characterize these five constructs. Our results suggest that these variables and these 5 domains may lead to a more systematic and optimized interpretation of isokinetic assessments. .

Regulatory volume decrease in Leishmania mexicana: effect of anti-microtubule drugs

The trypanosomatid cytoskeleton is responsible for the parasite's shape and it is modulated throughout the different stages of the parasite's life cycle. When parasites are exposed to media with reduced osmolarity, they initially swell, but subsequently undergo compensatory shrinking referred to as regulatory volume decrease (RVD). We studied the effects of anti-microtubule (Mt) drugs on the proliferation of Leishmania mexicana promastigotes and their capacity to undergo RVD. All of the drugs tested exerted antiproliferative effects of varying magnitudes [ansamitocin P3 (AP3)> trifluoperazine > taxol > rhizoxin > chlorpromazine]. No direct relationship was found between antiproliferative drug treatment and RVD. Similarly, Mt stability was not affected by drug treatment. Ansamitocin P3, which is effective at nanomolar concentrations, blocked amastigote-promastigote differentiation and was the only drug that impeded RVD, as measured by light dispersion. AP3 induced 2 kinetoplasts (Kt) 1 nucleus cells that had numerous flagella-associated Kts throughout the cell. These results suggest that the dramatic morphological changes induced by AP3 alter the spatial organisation and directionality of the Mts that are necessary for the parasite's hypotonic stress-induced shape change, as well as its recovery.

Renal ischemia and reperfusion injury: influence of chorpromazine on renal function and lipid peroxidation / Lesão de isquemia e reperfusão renal: influência da clorpromazina na função renal e na peroxidação lipídica

PURPOSE: To evaluate the influence of chlorpromazine (CPZ) on renal function and lipid peroxidation in a rat model of kidney ischemia/reperfusion injury. METHODS: Forty eight Wistar rats underwent a laparotomy for hilar clamping of left kidney with a bulldog clamp for 60 minutes followed by organ reperfusion and contralateral nephrectomy. Of these, 26 received 3mg/kg of CPZ intravenously 15 minutes before renal ischemia (G-E) while the remaining 22 were used as ischemic control group (G-C). Eleven rats of G-E and 8 of G-C were followed for blood urea nitrogen and creatinine determinations before renal ischemia and at 1st, 4th and 7th postoperative days. Samplings of left renal tissue were obtained at 5 minutes (5 rats from each group) and 24 hours (9 G-C and 10 of G-E) of reperfusion for malondialdehy (MDA) content determination. Controls of renal MDA content were determined in kidneys harvested from 6 additional normal rats. RESULTS: Acute renal failure occurred in all animals but levels of BUN and creatinine were significantly lower in G-E (p<0.001). MDA content rose strikingly at 5 minutes of reperfusion in both groups (p>0.05) and returned near to normal levels 24 hours later. CONCLUSION: CPZ conferred partial protection of renal function to kidneys submitted to ischemia/reperfusion injury that seems to be not dependent on inhibition of lipid peroxidation.

OBJETIVO: avaliar a influência da clorpromazina (CPZ) na função renal e na peroxidação lipídica num modelo de lesão de isquemia/reperfusão renal em ratos. MÉTODOS: 48 ratos Wistar foram submetidos à laparotomia para clampamento da artéria renal esquerda durante 60 minutos, seguido da reperfusão e nefrectomia contralateral. Destes animais, 26 receberam 3 mg/kg de CPZ intravenosa 15 minutos antes da isquemia renal (G-E), sendo os 22 animais restantes utilizados como grupo controle isquêmico (G-C). Em 11 ratos do G-E e 8 do G-C foi feita a dosagem de uréia e creatinina sérica antes da isquemia renal e no 1º, 4º e 7º dia pós-operatório. Amostras de tecido do rim esquerdo foram obtidas aos 5 minutos (5 ratos de cada grupo) e 24 horas após reperfusão (9 G-C e 10 G-E) para dosagem de malondialdeído (MDA). Valores controle para níveis de MDA foram obtidos em rins retirados de 6 ratos normais. RESULTADOS: insuficiência renal aguda ocorreu em todos os animais mas os níveis séricos de uréia e creatinina foram significativamente menores no G-E (p<0,001). Os níveis de MDA apresentaram elevação acentuada na avaliação aos 5 minutos de reperfusão em ambos os grupos (p<0,05), retornando a valores próximos aos normais na avaliação com 24 horas. CONCLUSÃO: a CPZ conferiu proteção parcial da função renal aos rins submetidos à lesão de isquemia e reperfusão, aparentemente independente da inibição da peroxidação lipídica.

Effect of chlorpromazine, imipramine and lithium on MAO-A and MAO-B activity in rat brain mitochondria.

Drugs with efficacy in psychiatric disorders affect the function of central neurotransmitter amines, which are inactivated primarily by monoamine oxidase (MAO). Effect of these drugs on the two types of MAO (MAO-A and MAO-B) has been studied in rat brain. The result showed that chlorpromazine (CPZ) and imipramine (IMI) at concentrations of 1x10(-2), 5x10(-3) and 2.5x10(-3) M inhibited rat brain mitochondrial MAO-A activity in vitro by 82, 50, 39 and 86, 74, 38 %, respectively. CPZ at concentrations of 5x10(-3), 2.5x10(-3), 1x10(-3) M inhibited rat brain mitochondrial MAO-B activity in vitro by 83, 55, 39 %, respectively, while IMI at concentrations of 5x10(-4), 2.5x10(-4), 1x10(-4) M inhibited the in vitro enzyme activity by 43, 35, 21 %, respectively. Lithium at concentration of 5x10(-3) M could not either inhibit MAO-A or MAO-B in the mitochondrial fraction of rat brain.

Darkened Xenopus tadpoles appeared with neurochemical agents.

Skin darkened tadpoles sometimes appear spontaneously. Darkened was artificially induced in Xenopus larvae by yohimbine or chlorpromazine. These phenomena look like that are seen at pinealectomized or hypothalamus separated Xenopus larva. In this experiment, such a morphological color changed Xenopus larva is suggested by cause of inhibition of alpha2-adrenargic receptor or dopamine receptor from gastrula stages.

Conscious sedation for pediatric cardiac catheterization

Diagnostic procedures make up a major portion of the practice of pediatric cardiology. Patient cooperation, often for extended periods, is of utmost importance for successful complication of many pediatric cardiac diagnostic procedures particularly those involving infants and preschool-age children. This requires the use of sedation. Invasive procedures such as cardiac catheterization and transesophageal echocardiography may cause significant discomfort, necessitating the use of additional analgesic and amnesic agents. Multiple drugs or repeated dose may be required during lengthy procedures. Ensuring patient safety by appropriate cardiorespiratory monitoring is mandatory. This review focuses on the pharmacologic agents used in pediatric cardiac catheterization. The pharmacology, indications for usage, and the risks and benefits of commonly used agents are addressed

Antipsychotic profile of alstonine: ethnopharmacology of a traditional Nigerian botanical remedy

Although recently developed drugs have brought significant improvement, the treatment of psychotic disorders still presents serious drawbacks. Since inherent complexity and lack of satisfactory understanding of the underlying pathophysiology impose limits for rational drug design, resourceful approaches in the search for antipsychotics are pertinent. This paper reports pharmacological properties of alstonine, a heteroyohimbine type alkaloid, Which exbitited an antipsychotic-like profile, inhibiting amphetamine-induced lethaly, apomorphine-induced steotypy and potentiating barbiturate-induced slleping time. Atypical features of alstonine were the prevention of haloperidol-induced catalepsy and lack of direct interaction with D1, D2 and 5-HT2A receptors, classically linked to antipsychotic mechanism of action.

A clinical study to assess chlorpromazine as hypoxic cell sensitizer in head & neck cancer treated with conventional radiation.

A randomized prospective study was conducted to evaluate the effectiveness of chlorpromazine as a sensitizer of radiation in advanced head and neck cancers. Patients with unresectable laryngopharyngeal cancers except glottic cancers, with histologically proven squamous cell carcinoma staged III and IV were accrued for the study. Patients received radiation to a total dose of 6000 cGy in six weeks in both the groups except that patients in the study group received 50 mgs Chlorpromazine (CPZ) in divided doses. Fourteen of 20 patients showed complete response in the control group whereas 34 of 38 patients in chlorpromazine treated group had complete regression of the tumour (p = 0.016). The survival was (p = 0.08) better in patients receiving CPZ. This preliminary study shows beneficial effects of chlorpromazine. No adverse effects due to chlorpromazine in conjunction with radiation were documented.

Pré-condicionamento precoce da medula espinal isquêmica: pesquisa em coelhos / Early preconditioning of the ischemic spinal cord: experimental study in rabbits

Investigou-se a possibilidade de desencadear o fenômeno do pré-condicionamento, imediatamente antes do esquemia de 30 minutos, como meio adicional de proteçao medular nos casos de pinçamento aórtico prolongado. Oitenta e sete coelhos da raça Nova Zelândia, distribuídos em 6 grupos, foram estudados. A isquemia medular resultou do pinçamento (P) da aorta abdominal, imediatamente após a origem da artéria renal esquerda. Estimulou-se o pré-condicionamento por curtos e repetidos períodos de isquemia, assinalados no texto por grifo, seguidos por variáveis tempos de reperfusao. Grupo I - Controle: 20 animais tiveram a aorta pinçada por 30 min. Dois (10 por cento) recuperaram integralmente a motricidade e a sensibilidade das patas posteriores e cauda; 18 (90 por cento) tornaram-se paraplégicos. Grupo II - Operaçao simulada: 10 (100 por cento) animais operados como os do grupo anterior, exceto pelo nao pinçamento da aorta, recuperaram plenamente as funçoes sensitivo-motoras. Grupo III - Pré-condicionamento: 10 animais - (P) 1 min r15 min r(P) 30 min r reperfusao final. Todos (100 por cento) tornaram-se paraplégicos. Grupo IV - Pré-condicionamento: 6 animais - (P) 1 min r 5 min r (P) 2 min r 5 min r(P) 2 min r 5 min (P) 30 min _ reperfusao final. Cinco (83,33 por cento) coelhos ficaram paraplégicos e 1 (16,66 por cento) ficou monoplégico. Grupo V - Clorpromazina: 20 animais receberam clorpromazina por via endovenosa, na dose de 2 mg/Kg peso, 10 min antes do pinçamento aórtico. Onze (55 por cento) tiveram recuperaçao sensitivo-motora integral e 9 (45 por cento), ficaram paraplégicos. Grupo VI - Clorpromazina + pré-condicionamento: 21 animais receberam a clorpromazina como os do grupo anterior, sendo pré-condicionados da forma (P) 1 min r 5 min r(P) 1 min r 5min r(P) 30 min r reperfusao final. Nove 42,8 por cento) tiveram recuperaçao sensitivo-motora integral e 2 (9,52 por cento), recuperaçao parcial. Os demais (47,68 por cento) ficaram paraplégicos. A análise estatística demonstrou nao haver diferença significativa entre os resultados dos grupos III e IV, e quando ambos foram comparados com o grupo I. Nao foi significativa a diferença entre os grupos V e VI, mas foi significativa quando ambos foram comparados com o grupo I (p<0,05). Estudo histológico - Outros 12 animais foram usados exclusivamente para o estudo histológico sob microscopia óptica: 6 do grupo controle e 6 com pré-condicionamento...

Effects of calcium on phthalocyanine sensitized photohemolysis.

Influence of divalent Ca2+ ions in sulphonated chlorophthalocyanine (ClAlPcS2) induced photohemolysis in rabbit red blood cells has been investigated. Loading of excess Ca2+ to ClAlPcS2 sensitized RBC suspension enhanced hemolysis in a concentration dependent manner. Protein kinase C (PKC) inhibitor chlorpromazine and cation chelator EDTA reduced Ca2+ enhanced photohemolysis. Photohemolysis increased with calcium channel blockers diltiazem and nifidipine. Enhancement in photohemolysis by Ca2+ ions can arise either by its ability to liberate Fe2+ bound to phosphatidylserine or by stimulation of PKC. Inability of calcium channel blockers to prevent Ca2+ influx following photodynamic treatment of red blood cells suggest nonspecific leakage rather than involvement of Ca2+ channels in erythrocytes.

Efectos de la Hindarina sobre las aurículas aisladas / Effects on hindarine on the isolated atria

Se presentan los efectos de la hindarina y de la clorpromacina sobre la amplitud y la frecuencia de las contracciones espontáneas de la aurículas aisladas de rata. La hindarina produjo bradicardia moderada y aumento discreto de la amplitud de las contracciones en forma dosis-dependiente, en tanto que la clorpromacina deprimió más intensamente tanto la frecuencia como la amplitud de dichas contracciones. Se descartó una acción colinérgica o beta-bloqueadora en la producción de la bradicardia por la hindarina. Se descartó también una acción cardiotónica de la hindarina en las aurículas aisladas de cobayo deprimidas por solución hipocálcica o por hipoxia. Se sugiere su estudio como antiarrítmico

Decanoato de flupentixol versus otros neurolépticos en esquizofrénicos crónicos / Flupentixol decanoate versus other neuroleptics in chronic schizophrenia

El estudio fue realizado en 80 pacientes ambulatorios del Servicio de Psiquiatría del Hospital Salvador (Santiago, Chile) con diagnóstico de esquizofrenia crónica según los criterios del DSM-IV. 40 pacientes fueron tratados con decanoato de flupentixol (como monoterapia neuroléptica). Los 40 restantes (grupo control) fueron tratados con uno o más de los siguientes neurolépticos: clorpromazina, haloperidol, tioridazina, decanoato de flufenazina. Ambos grupos fueron evaluados en entrevistas psiquiátricas y psicológicas utilizando 7 escalas estandarizadas. El uso de decanoato de flupentixol redujo los síntomas positivos y negativos que caracterizan a la esquizofrenia, corroborado por escalas BPRS y CGI.La adhesión al tratamiento con decanoato de flupentixol fue mejor y los efectos colaterales fueron escasos. El grupo control requirió el uso de uno o más neurolépticos para lograr la estabilización o reducción de los síntomas, con la consecuente presentación de efectos colaterales en un mayor número de casos. Finalmente, los resultados positivos obtenidos con decanoato de flupentixol están relacionados con la intensidad de la sintomatología. La efectividad de la medicación fue interior en los pacientes que desarrollaron crisis psicóticas y/o en los pacientes resistentes al tratamiento neuroléptico

Effects of oral lithium on the action of various C.N.S. active drugs.

Effects of prolonged lithium administration was seen on the action of various psychoactive drugs in animals. Apomorphine induced pecking in pigeons increased significantly by lithium treatment for 14 days, from 1445.3 +/- 202.5 in control to 2785.8 +/- 205.8 in Gp. B. Haloperidol-induced catalepsy score in albino rats increased significantly following chronic lithium treatment compared to control. Chlorpromazine-induced hypothermia in rabbits was immediate but transient, while in lithium treated rabbits induction of hypothermia was delayed, sustained and of greater magnitude. This action of lithium may be mediated by increasing the permeability of blood-brain barrier, or enhancing the sensitivity of alpha-adrenoceptors in brain.

Proteçäo farmacológica da medula espinal isquêmica / Pharmacological protection of the ischemic spinal cord

Estudou-se a açao protetora da quetamina (30mg/Kg, EV) e da clorpromazina (2mg/Kg,EV), sobre a medula espinal de ratos Wistar, submetida à isquemia de 30 min, por oclusao da aorta torácica, seguida de reperfusao. Em 70 animais, com peso médio de 380g, divididos em 7 grupos iguais, obtiveram-se os seguintes resultados porcentuais referentes à integral recuperaçao sensitivo-motora: 1) "Sham-operation": 100 por cento; 2) isquemia-reperfusao: 0 por cento; 3) quetamina, 1 min antes da isquemia: 30 por cento; 4) quetamina, 10 min. antes da isquemia: 50 por cento; 5) clorpromazina, 1 min antes da isquemia: 50 por cento; 6) clorpromazina, 1 min. antes da reperfusao: 10 por cento; 7) quetamina+clorpromazina, 1 min antes da isquemia: 60 por cento. Tanto a quetamina quanto a clorpromazina protegeram parte dos animais cuja medula espinal fora submetida à isquemia-reperfusao. Contudo, ao se comparar os animais protegidos, as diferenças de resultados só alcançaram significância estatística entre os grupos 6 e 7. O estudo histológico, por microscopia óptica, confirmou a açao protetora de ambos os agentes farmacológicos. A perfusao do espaço subaracnóideo dos animais cuja medula espinal fora submetida à isquemia-reperfusao demonstrou quantidade excessiva dos aminoácidos neuroexcitadores, L-aspartato e L-glutamato.

Cyclodiene insecticides-induced changes in the central depressive effect of chlorpromazine in rats.

Spontaneous motor activity (SMA), conditioned avoidance response (CAR), muscle coordination (MC) and pentobarbital sleep were tested in rats treated orally for 90 days with tolerated doses of the cyclodiene insecticides, aldrin (1 mg/kg) and endosulfan (2 mg/kg). The same tests were repeated in similarly treated animals after injecting chlorpromazine (4 mg/kg, i.p.). Both the insecticides shortened pentobarbital sleeping time indicating their microsomal enzyme inducing property. Aldrin suppressed SMA, CAR and MC, whereas endosulfan stimulated SMA, inhibited CAR and unaltered MC. However, their concurrent action with CPZ did not result in change in the central depressive effects of the latter, but its potency during the course of its action was altered. Its potency 15 min after injection was greater and 60-180 min later was lesser in these animals than that observed in control animals. This finding was interpreted to suggest that aldrin and endosulfan has quickened the biotransformation of CPZ and thereby shortened its duration of action. A temporary promotion of its potency was accounted to its active metabolites, since prior to inactivation, CPZ is known to be metabolized by the microsomal enzymes to active compounds.

Parasympatholytic activity of psychoactive drugs in rat brain mitochondria.

Chlorpromazine, imipramine and amphetamine at a concentration of 0.66, 1.33 and 13.3 x 10(4) M in vitro inhibited acetyl cholinesterase activity by 16, 23 and 31% respectively in rat brain mitochondria. No change in enzyme activity was induced by these drugs in vivo. There is little cholinergic facilitation through acetylcholinesterase inhibition in the presence of psychoactive drugs.

Efeitos oculares associados ao padräo de uso e à dose de clorpromazina / Ocular effects related to the pattern and dose of use chlorpromazine

Os autores avaliam a influência da dose da clorpromazina no desenvolvimento de alteraçöes oculares características em 38 pacientes psiquiátricos internados no Hospital Psiquiátrico Säo Pedro (Porto Alegre, RS) em uso crônico desta droga. Vinte e dois pacientes (58 por cento) apresentaram efeitos oculares adversos, manifestados por opacificaçäo bilateral do cristalino e, em casos severos, opacificaçäo concomitante do endotélio corneano. Os pacientes foram classificados em graus crescentes de 0 a IV pigmentaçäo bilateral acentuada da cápsula anterior do cristalino em forma de estrela. A frequência das alteraçöes é analisada em relaçäo faixa etária, padräo de uso e doses utilizadas. Os autores sugerem a possibilidade de uma suscetibilidade maior em indivíduos idosos, e concluem ser a dose de clorpromazina o fator mais importante na gênese das alteraçöes oculares