Temperature central blood

Alteration of vita signs (temperature, pulse rate, respiratory rate, blood pressure) Central nervous system hallucination, convulsions, coma, ataxia, paralysis Teratogenesis Mutagenesis Carcinogenesis Effects on immune system... 

During hyperthermia, terms representing the heat input to a specific tissue or whole body must be added to the proper system equation(s). For example, during whole-body or local hyperthermia induced by radiofrequency currents, microwaves, or ultrasound, a heat-generation term is added to the section of the body being heated. During hyperthermia with blood perfusion, the afferent blood temperature is set at a desired value, and the efferent blood is circulated to the central blood pool, or to the extracorporeal device used for heating the blood. Suitable numerical... 

Initial safety tests were carried out in beagle dogs and subsequently in cynomolgus monkeys. Single bolus i.v. doses of up to 100 mg kg-1 were used and were found to exert no negative effect upon general condition, blood pressure, heart or cardiovascular parameters, respiration rate or body temperature. No safety tests evaluating potential product effects upon the central nervous system were undertaken, as the protein is considered unlikely to cross the blood-brain barrier. 

Since GABA-ergic synapses are confined to neural tissues, specific inhibition of central nervous functions can be achieved for instance, there is little change in blood pressure, heart rate, and body temperature. The therapeutic index of benzodiazepines, calculated with reference to the toxic dose producing respiratory depression, is greater than 100 and thus exceeds that of barbiturates and other sedative-hypnotics by more than tenfold. Benzodiazepine intoxication can be treated with a specific antidote (see below). 

Serotonin, also called 5-hydroxytryptamine, is synthesized and stored at several sites in the body (Figure 21.18). By far the largest amount of serotonin is found in cells of the intestinal mucosa. Smaller amounts occur in platelets and in the central nervous system. Serotonin is synthesized from tryptophan, which is hydroxy-lated in a reaction analogous to that catalyzed by phenylalanine hydroxylase. The product, 5-hydroxytryptophan, is decarboxylated to serotonin. Serotonin has multiple physiologic roles, including pain perception, affective disorders, and regulation of sleep, temperature, and blood pressure. 

The baroreceptor response is just one example of the type of reflex activity employed by the ANS. The control of other involuntary functions usually follows a similar pattern of peripheral monitoring, central integration, and altered autonomic discharge. Body temperature, for instance, is monitored by thermoreceptors located in the skin, viscera, and hypothalamus. When a change in body temperature is monitored by these sensors, this information is relayed to the hypothalamus and appropriate adjustments are made in autonomic discharge in order to maintain thermal homeostasis (e.g., sweating is increased or decreased and blood flow is redistributed). Many other autonomic reflexes that control visceral and involuntary functions operate in a similar manner. 

Colchicine also exhibits a variety of other pharmacological effects. It lowers body temperature, increases the sensitivity to central depressants, depresses the respiratory center, enhances the response to sympathomimetic agents, constricts blood vessels, and induces hypertension by central vasomotor stimulation. It enhances gastrointestinal activity by neurogenic stimulation but depresses it by a direct effect, and alters neuromuscular function. 

Cocaine is a central nervous system (CNS) stimulant that causes a significant increase in heart rate, respiration, blood pressure, and body temperature. According to DAWN, one in thirteen cocaine users go to the hospital to be treated for severe reactions that could be life-threatening. Sudden death can result from heart failure, respiratory failure, seizures, strokes, and cerebral hemorrhage. There is no antidote for cocaine overdose. Even if the adverse reactions do not result in death, they can do permanent damage to the body. 

Side effects, such as headache and jaw pain, are observed, but the major drawbacks with epoprostenol therapy relate to its delivery. Epoprostenol has an extremely short half-life in the blood (2-3 min) and therefore must be administered by continuous intravenous infusion via a surgically implanted central vein catheter. This can lead to complications such as local infections, sepsis, or catheter-associated thrombosis. In addition, interruption of therapy due, for example, to pump failure can lead to a life-threatening rebound of symptoms. The compound itself is unstable at room temperature and must be stored in the refrigerator. Despite these severe drawbacks, i.v. epoprosenol remains a useful treatment for patients presenting with WHO class IV PAH. The problems with epoprostenol have led to the development of alternative agents. 

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