SUMMARY1. We recorded the electrical activity of single afferent cardiac fibres isolated from the third and fourth left thoracic sympathetic rami communicantes of anaesthetized cats. Their conduction velocities ranged from 12 to 32 m/sec.2. The endings of each fibre were localized to one cardiac chamber by mechanical probing of the opened heart performed at the end of the experiment.3. The impulse activity was spontaneous and, in fibres with atrial or ventricular endings, it was in phase with a particular atrial or ventricular event.4. This nervous activity increased during increases in pressure occurring in the chamber where the endings were located. Conversely, decreases in pressure were accompanied by decreased nervous discharge.5. In some experiments the left coronary artery was perfused at different flows and pressures. Brief decreases or increases in coronary flow and pressure decreased or increased, respectively, the discharge of fibres with atrial or ventricular endings. Fibres were excited by intracoronary mijections of veratridine.6. Cessation of coronary pump flow increased the discharge of fibres with atrial or ventricular endings only when myocardial ischaemia was accompanied by signs of heart failure.7. These afferent cardiac sympathetic fibres which provide the spinal cord with continuous specific information on cardiac events are likely to contribute to the neural control of circulation.

SUMMARY Two major groups of renal chemosensory neural elements have been identified in the rat: one specifically activated by renal ischemia, the previously described "R" chemoreceptors, and the other by backflow of nondiuretic urine into the renal pelvis. The latter group is the object of the present investigation. In anesthetized, male Sprague-Dawley rats, single-unit recordings were obtained by dissection of the centrally cut nerves of the right kidney. The responses of single units to backflow into the renal pelvis of nondiuretic urine, diuretic urine, and solutions containing urea, mannitol, or inorganic ions were compared. The excitatory effect of the backflow of nondiuretic urine was due to its chemical composition rather than to changes in pelvic pressure and pelvic distension. The same units were activated markedly by renal ischemia. The resting discharge rate of the units was very high in nondiuretic conditions, and it declined progressively when diuresis was induced by expansion of the extracellular fluid volume. It is concluded that this group of sensory elements responds to the chemical environment in the renal interstitium as modified by ions crossing the pelvic epithelium, by leakage of ions out of ischemic cells, and by alterations in the excretory function of the kidney and renal blood flow. This group of renal sensory nerve endings has been termed "R2" chemoceptive receptors, to distinguish them from the previously described group of renal "R" chemoreceptors. Circ Res 46: 395-405, 1980LIKE OTHER visceral organs, the kidneys have a profuse sensory innervation. From recordings of impulses conducted along afferent fibers in the renal nerves, several functional classes of renal sensory receptors have been identified so far. In cats, there are receptors sensitive to alterations in ureteral pressure and to venous or arterial perfusion pressure (Beacham and Kunze, 1969;Astrom and Crafoord, 1968); in rabbits, receptors affected by changes in ureteral and arterial perfusion pressure, but not changes in venous pressure (Niijima, 1971); in dogs, units responsive to changes in venous, ureteral, or arterial perfusion pressure (Uchida et al., 1971); in rats, receptors sensitive to increase in venous pressure (Astrom and Crafoord, 1967). In the renal nerves of the rat at least two other populations exist. The fibers of one group are silent under control conditions and are activated only by renal ischemia; those of the other population exhibit a resting discharge and respond markedly to backflow of urine into the renal pelvis (Recordati et al., 1978 characteristics of the first group of receptors which, because of their sensitivity to ischemia and unresponsiveness to mechanical stimuli, were termed renal, "R," chemoreceptors. The second group, on the other hand, was analyzed only superficially. They were considered to be a population of renal mechanoreceptors because previous investigators (Beacham and Kunze, 1969;Astrom and Crafoord, 1968;Niijima, 1971) had thought that changes in pelvic pressure and pelvic d...

In light of the nonequilibrium thermodynamics by I. Prigogine, the autonomic nervous system as a whole may be viewed as a dissipative structure progressively assembled in the course of evolution, plastically and rhythmically interfaced between forebrain, internal and external environments, to regulate energy, matter and information exchanges. In the present paper, this hypothesis is further pursued to verify whether the two main divisions of the autonomic nervous system, the sympathetic and parasympathetic systems, may support different types of exchange with the external environment. Previous data from hypothalamic stimulation experiments, studies of locus coeruleus function and available data on behavioral functional organization indicate that (1) tight engagement with the external environment, (2) high level of energy mobilization and utilization and (3) information mainly related to exteroceptive sensory stimulation characterize a behavioral prevalence of sympathoadrenal activation. On the other hand, (1) disengagement from the external environment, (2) low levels of internal energy and (3) dominance of proprioceptive information characterize a behavioral prevalence of vagal tone. Behavioral matter exchanges such as feeding, drinking, micturition and defecation are equally absent at the extreme of sympathoadrenal and vagally driven behaviors. The autonomic nervous system as a whole is genetically determined, but the sympathoadrenal system has been mainly designed to organize the visceral apparatus for an action to be performed by the biological system in the external environment and to deal with the novelty of task and of the environment, while the functional role of the parasympathetic is to prepare the visceral apparatus for an action to be performed by the biological system on itself, for recovery and self-protection (homeostasis), and is reinforced by repetition of phylo- and ontogenetically determined patterns. The available clinical data further support this interpretation indicating that an increased sympathetic and a decreased vagal tone may represent a consistent risk factor for cardiovascular diseases.

There are afferent nerve fibers responsive to alterations of the kidney's chemical environment in the renal nerves of the rat. In anesthetized, artificially ventilated, male Sprague-Dawley rats, single unit recordings were prepared by dissection of the centrally cut nerves of the right kidney. The stimuli used included occlusion of the renal artery, systemic asphyxia, changes in renal arterial and venous pressures, changes in ureteral pressure, and cyanide infusion. We found a population of sensory nerve fibers whose endings are activated only during markedly impaired renal blood flow (produced by clamping the renal artery, severe hypotension below 40 mm Hg, and prolonged occlusion of the renal vein), and during systemic asphyxia. The same units are not responsive to increases and decreases in systemic arterial pressure (range: 40--190 mm Hg), to ureteral pressure (range: 0--50 mm Hg), or to changes in renal venous pressure. None of the 40 single units studied was spontaneously active; their pattern of activation during renal ischemia always was characterized by trains of impulses. These sensory units have functional properties distinctly different from those of known renal mechanoreceptors. They appear to be a homogeneous group of sensory elements, and we have termed them renal ("R") chemoreceptors. Evidence also is presented which is consistent with the concept that a chemical substance released by or accumulated within the kidney might be the agent activating these chemoreceptors during renal ischemia.

The constancy of the internal environment, internal homeostasis, and its stability are necessary conditions for the survival of a biological system within its environment. These have never been clearly defined. For this purpose nonequilibrium thermodynamics is taken as a reference, and the essential principles of equilibrium, reversibility, stationary steady state and stability (Lyapounov, asymptotic, local and global), are briefly illustrated. On this basis, internal homeostasis describes a stationary state of nonequilibrium, the actual state of rest, X(t), resulting from the relation X(t) = X S + x(t), between a time-independent steady state of reference (X S ), and time-dependent fluctuations of the state variables, x(t). In humans, two resting spontaneous homeostatic states are: (1) the conscious state of quiet wakefulness, during which time-dependent variables display bounded oscillations around the mean time-independent steady state level, this conscious state being thus stable in the sense of Lyapounov, and (2) the unconscious stable state of nonrapid eye movement sleep, in which the time-dependent variables would approach the lowest spontaneously attainable time-independent state asymptotically, sleep becoming a globally stable and attractive state. Exercise may be described as a non-resting, unstable active state far away from equilibrium and hibernation is a resting, time-independent steady state very near equilibrium. The range between sleep and exercise is neurohumorally regulated. For spontaneously stable states to occur, slowing of the metabolic rate, withdrawal of the sympathetic drive and reinforcement of the vagal tone to the heart and circulation are required, thus confirming that the parasympathetic division of the autonomic nervous system is the main controller of homeostasis.