RESUMEN
Recent studies have demonstrated that a mild stimulation of the dorsomedian nucleus of the hypothalamus (DMH), a defense area, induces the inhibition of the carotid chemoreflex tachypnea. DMH activation reduces the cardiac chemoreflex response via the dorsolateral part of the periaqueductal grey matter (dlPAG) and serotonin receptors (5-HT3 subtype) in the nucleus tractus solitarius (NTS). The objectives of this study were to assess whether dlPAG and subsequent NTS 5-HT3 receptors are involved in chemoreflex tachypnea inhibition during mild activation of the DMH. For this purpose, peripheral chemoreflex was activated with potassium cyanide (KCN, 40 µg/rat, i.v.) during electrical and chemical minimal supra-threshold (mild) stimulation of the dlPAG or DMH. In both situations, changes in respiratory frequency (RF) following KCN administration were reduced. Moreover, pharmacological blockade of the dlPAG prevented DMH-induced KCN tachypnea inhibition. Activation of NTS 5-HT3 receptors also reduced chemoreflex tachypnea in a dose-dependent manner. In addition, blockade of NTS 5-HT3 receptors with granisetron (2.5 but not 1.25 mM), or the use of mice lacking the 5-HT3a receptor (5-HT3a KO), prevented dlPAG-induced KCN reductions in RF. A respiratory hypothalamo-midbrain-medullary pathway (HMM) therefore plays a crucial role in the inhibition of the hyperventilatory response to carotid chemoreflex.
Asunto(s)
Barorreflejo/efectos de los fármacos , Células Quimiorreceptoras/efectos de los fármacos , Inhibidores Enzimáticos/farmacología , Cianuro de Potasio/farmacología , Respiración/efectos de los fármacos , Médula Suprarrenal , Animales , Biguanidas/farmacología , Relación Dosis-Respuesta a Droga , Hipotálamo/efectos de los fármacos , Hipotálamo/fisiología , Masculino , Ratones , Ratones Endogámicos C57BL , Ratones Transgénicos , Vías Nerviosas/efectos de los fármacos , Vías Nerviosas/fisiología , Ratas , Ratas Sprague-Dawley , Receptores de Serotonina 5-HT3/deficiencia , Receptores de Serotonina 5-HT3/genética , Agonistas de Receptores de Serotonina/farmacología , Núcleo Solitario/efectos de los fármacos , Núcleo Solitario/fisiologíaRESUMEN
The impact of neonicotinoid insecticides on insect pollinators is highly controversial. Sublethal concentrations alter the behaviour of social bees and reduce survival of entire colonies. However, critics argue that the reported negative effects only arise from neonicotinoid concentrations that are greater than those found in the nectar and pollen of pesticide-treated plants. Furthermore, it has been suggested that bees could choose to forage on other available flowers and hence avoid or dilute exposure. Here, using a two-choice feeding assay, we show that the honeybee, Apis mellifera, and the buff-tailed bumblebee, Bombus terrestris, do not avoid nectar-relevant concentrations of three of the most commonly used neonicotinoids, imidacloprid (IMD), thiamethoxam (TMX), and clothianidin (CLO), in food. Moreover, bees of both species prefer to eat more of sucrose solutions laced with IMD or TMX than sucrose alone. Stimulation with IMD, TMX and CLO neither elicited spiking responses from gustatory neurons in the bees' mouthparts, nor inhibited the responses of sucrose-sensitive neurons. Our data indicate that bees cannot taste neonicotinoids and are not repelled by them. Instead, bees preferred solutions containing IMD or TMX, even though the consumption of these pesticides caused them to eat less food overall. This work shows that bees cannot control their exposure to neonicotinoids in food and implies that treating flowering crops with IMD and TMX presents a sizeable hazard to foraging bees.
Asunto(s)
Abejas/fisiología , Dieta/veterinaria , Preferencias Alimentarias , Insecticidas/análisis , Néctar de las Plantas/química , Animales , Abejas/efectos de los fármacos , Células Quimiorreceptoras/efectos de los fármacos , Células Quimiorreceptoras/metabolismo , Femenino , Flores/química , Flores/efectos de los fármacos , Preferencias Alimentarias/efectos de los fármacos , Guanidinas/efectos adversos , Guanidinas/análisis , Guanidinas/farmacología , Imidazoles/efectos adversos , Imidazoles/análisis , Imidazoles/farmacología , Insecticidas/efectos adversos , Insecticidas/farmacología , Masculino , Neonicotinoides , Nitrocompuestos/efectos adversos , Nitrocompuestos/análisis , Nitrocompuestos/farmacología , Oxazinas/efectos adversos , Oxazinas/análisis , Oxazinas/farmacología , Polen/química , Polinización , Reproducción/efectos de los fármacos , Reproducción/fisiología , Análisis de Supervivencia , Gusto/fisiología , Tiametoxam , Tiazoles/efectos adversos , Tiazoles/análisis , Tiazoles/farmacologíaRESUMEN
The swallowtail butterfly, Papilio xuthus, selectively uses a limited number of plants in the Rutaceae family. The butterfly detects oviposition stimulants in leaves through foreleg chemosensilla and requires a specific combination of multiple oviposition stimulants to lay eggs on the leaf of its host plants. In this study, we sought to elucidate the mechanism underlying the regulation of oviposition behavior by multiple oviposition stimulants. We classified chemosensilla on the tarsomere of the foreleg into three types (L1, L2, and S) according to their size and response to oviposition stimulants and general tastants. The L1 was more abundant in females than in males and responded preferentially to oviposition stimulants. Both L2 and S were common to both sexes and responded to general tastants. We found that five oviposition stimulants (synephrine, stachydrine, 5-hydroxy-Nω-methyltryptamine, narirutin, and chiro-inositol) elicited spikes from three specific gustatory receptor neurons (GRNs) within L1 sensilla. These three GRNs responded to a mixture of the five stimulants at concentrations equivalent to those found in the whole-leaf extract of citrus, and the mixture induced oviposition at levels comparable to whole-leaf extract. We propose that oviposition is triggered by the firing of three specific GRNs in L1 sensilla that encode the chemical signatures of multiple oviposition stimulants.
Asunto(s)
Mariposas Diurnas/fisiología , Células Quimiorreceptoras/fisiología , Oviposición/fisiología , Sensilos/fisiología , Gusto/fisiología , Animales , Conducta Animal/efectos de los fármacos , Conducta Animal/fisiología , Mariposas Diurnas/efectos de los fármacos , Células Quimiorreceptoras/efectos de los fármacos , Femenino , Oviposición/efectos de los fármacos , Extractos Vegetales/farmacología , Rutaceae , Sensilos/efectos de los fármacos , Gusto/efectos de los fármacosRESUMEN
Orexin neurons form a restricted group in the dorsal hypothalamus. The group is centered on the perifornical area within the classic hypothalamic defense area, an area which when activated produces marked cardiovascular and respiratory effects. Central administration of orexin can produce cardiorespiratory effects, but the extent to which orexin contributes to such responses evoked from the perifornical hypothalamus is not clear. To determine this, we used the dual orexin receptor antagonist Almorexant to challenge the cardiorespiratory effects evoked by disinhibition of the perifornical hypothalamus. Bicuculline (10 and 20 pmol) was microinjected in the perifornical area before and after administration of Almorexant (15 mg/kg iv) or vehicle in urethane-anesthetized rats. Almorexant significantly reduced the pressor, tachycardic, renal sympathoexcitatory, and tachypneic responses to bicuculline (10 pmol, by 55%, 53%, 28%, 77%; 20 pmol, by 54%, 27%, 51%, 72%, respectively). Reductions of similar magnitude were observed with bicuculline microinjections centered on more caudal sites just peripheral to the orexin neuron group, which would likely have activated fewer orexin neurons. In contrast, Almorexant had no effect on the cardiorespiratory response of the chemoreflex (sodium cyanide injection) or the sympathetic component of the baroreflex. Thus orexin makes a major contribution to the cardiorespiratory response evoked from the perifornical area even though orexin neurons represent only a fraction of the output of this area. Orexin neurons may also mediate cardiorespiratory responses from non-orexin neurons in the caudal hypothalamus. However, under resting conditions, blockade of orexin receptors does not affect the chemo- and baroreflexes.
Asunto(s)
Acetamidas/farmacología , Barorreflejo/efectos de los fármacos , Células Quimiorreceptoras/efectos de los fármacos , Hipotálamo/efectos de los fármacos , Isoquinolinas/farmacología , Receptores Acoplados a Proteínas G/antagonistas & inhibidores , Receptores de Neuropéptido/antagonistas & inhibidores , Animales , Bicuculina/farmacología , Relación Dosis-Respuesta a Droga , Antagonistas de Receptores de GABA-A/farmacología , Hipotálamo/fisiología , Masculino , Receptores de Orexina , Ratas , Ratas Sprague-DawleyRESUMEN
Nematocytes' discharge is triggered to perform both defense and predation strategies in cnidarians and occurs under chemico-physical stimulation. In this study, different compounds such as amino acids and proteins (mucin, albumin, poly-L: -lysine, trypsin), sugars and N-acetylate sugars (N-acetyl neuraminic acid, N-acetyl galactosamine, sucrose, glucose, agarose and trehalose), nucleotides (ATP and cAMP), were tested as chemosensitizers of nematocyte discharge in the oral arms of the scyphozoan Pelagia noctiluca, particularly abundant in the Strait of Messina (Italy). Excised oral arms were submitted to a combined chemico-physical stimulation by treatment with different compounds followed by mechanical stimulation by a non-vibrating test probe. Discharge induced by a chemico-physical stimulation was more significant than that obtained after mechanical stimulation alone. A chemosensitizing mechanism, with a dose-dependent effect, was observed after treatment with sugars, amino compounds such as glutathione, nucleotides and mucin, according to that already seen in sea anemones. Such findings suggest that, though Anthozoa and Scyphozoa exhibit different divergence times during the evolutionary process, the discharge activation exhibits common features, probably derived from their last common ancestor.
Asunto(s)
Células Quimiorreceptoras/fisiología , Nematocisto/fisiología , Escifozoos/fisiología , Transducción de Señal , Aminas/farmacología , Aminoácidos/farmacología , Animales , Calcio/metabolismo , Carbohidratos/farmacología , Células Quimiorreceptoras/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Mecanotransducción Celular , Nematocisto/citología , Nematocisto/efectos de los fármacos , Nucleótidos/farmacología , Estimulación Física , Proteínas/farmacología , Escifozoos/citología , Escifozoos/efectos de los fármacos , Transducción de Señal/efectos de los fármacos , Factores de TiempoRESUMEN
AIM OF THE STUDY: This study was aimed to evaluate the neuroprotective and anti-aging activity of extracts in Caenorhabditis elegans from the roots and leaves of Damnacanthus officinarum Huang to provide the pharmacological basis in traditional medicine. MATERIALS AND METHODS: Investigations on the neuroprotective and lifespan activity were carried out, which were observed by utilizing the following models: observing the worms' chemosensory behavior test based on the aversion index in the assay plate, neuroprotective activity of nematode by evaluating the ASH neuron survival and lifespan test in C. elegans. RESULTS: It has been shown that the ethanol, n-butanol and aqueous extracts in the roots possessed significantly neuroprotective effect both in chemosensory behavior test and ASH neuron survival model. The same extracts in the leaves showed similar activities in two models, but have less potency revealing by the data. Four candidate extracts, possessing excellent neuroprotective activity, extend lifespan in C. elegans. The n-butanol extracts in the root part showed best efficacy among them. CONCLUSION: The results show the n-butanol and aqueous extracts are the major pharmacological plant extracts. Moreover, the neuroprotective and lifespan-extension activity effects of root extracts are superior to leave extracts, supporting the traditional application of above-ground parts of DOH in treating various diseases associated with brain disorders and anti-aging.
Asunto(s)
Caenorhabditis elegans/efectos de los fármacos , Longevidad/efectos de los fármacos , Neuronas/efectos de los fármacos , Fármacos Neuroprotectores/farmacología , Extractos Vegetales/farmacología , Rubiaceae , 1-Butanol/química , Animales , Animales Modificados Genéticamente , Caenorhabditis elegans/genética , Caenorhabditis elegans/metabolismo , Supervivencia Celular/efectos de los fármacos , Células Quimiorreceptoras/efectos de los fármacos , Células Quimiorreceptoras/metabolismo , Relación Dosis-Respuesta a Droga , Etanol/química , Neuronas/metabolismo , Neuronas/patología , Fármacos Neuroprotectores/química , Fármacos Neuroprotectores/aislamiento & purificación , Fitoterapia , Extractos Vegetales/química , Extractos Vegetales/aislamiento & purificación , Hojas de la Planta , Raíces de Plantas , Plantas Medicinales , Rubiaceae/química , Solventes/química , Factores de TiempoRESUMEN
We have previously shown that hypercapnic chemoreflex in prepro-orexin knockout mice (ORX-KO) is attenuated during wake but not sleep periods. In that study, however, hypercapnic stimulation had been chronically applied for 6 h because of technical difficulty in changing the composition of the inspired gas mixture without distorting the animal's vigilance states. In the present study we examined possible involvement of orexin in acute respiratory chemoreflex during wake periods. Ventilation was recorded together with electroencephalography and electromyography before and after intracerebroventricular administration of orexin or an orexin receptor antagonist, SB-334867. A hypercapnic (5 or 10% CO(2)) or hypoxic (15 or 10% O(2)) gas mixture was introduced into the recording chamber for 5 min. Respiratory parameters were analyzed only for quiet wakefulness. When mice breathed normal room air, orexin-A and orexin-B but not vehicle or SB-334867 increased minute ventilation in both ORX-KO and wild-type (WT) mice. As expected, hypercapnic chemoreflex in vehicle-treated ORX- KO mice (0.22 +/- 0.03 mlxmin(-1)xg(-1)x% CO(2)(-1)) was significantly blunted compared with that in WT mice (0.51 +/- 0.05 mlxmin(-1)xg(-1)x% CO(2)(-1)). Supplementation of orexin-A or -B (3 nmol) partially restored the hypercapnic chemoreflex in ORX-KO mice (0.28 +/- 0.03 mlxmin(-1).g(-1)x% CO(2)(-1) for orexin-A and 0.32 +/- 0.04 mlxmin(-1)xg(-1)x% CO(2)(-1) for orexin-B). In addition, injection of SB-334867 (30 nmol) in WT mice decreased the hypercapnic chemoreflex (0.39 +/- 0.04 mlxmin(-1)xg(-1)x% CO(2)(-1)). On the other hand, hypoxic chemoreflex in vehicle-treated ORX-KO and SB-334867-treated WT mice was not different from that in corresponding controls. Our findings suggest that orexin plays a crucial role in CO(2) sensitivity at least during wake periods in mice.
Asunto(s)
Dióxido de Carbono/sangre , Células Quimiorreceptoras/metabolismo , Hipercapnia/metabolismo , Hipotálamo/metabolismo , Péptidos y Proteínas de Señalización Intracelular/metabolismo , Neuropéptidos/metabolismo , Ventilación Pulmonar , Receptores Acoplados a Proteínas G/metabolismo , Receptores de Neuropéptido/metabolismo , Reflejo , Animales , Benzoxazoles/administración & dosificación , Células Quimiorreceptoras/efectos de los fármacos , Células Quimiorreceptoras/fisiopatología , Modelos Animales de Enfermedad , Electroencefalografía , Electromiografía , Hipercapnia/fisiopatología , Hipotálamo/efectos de los fármacos , Hipotálamo/fisiopatología , Hipoxia/metabolismo , Hipoxia/fisiopatología , Inyecciones Intraventriculares , Péptidos y Proteínas de Señalización Intracelular/administración & dosificación , Péptidos y Proteínas de Señalización Intracelular/deficiencia , Péptidos y Proteínas de Señalización Intracelular/genética , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Actividad Motora , Naftiridinas , Neuropéptidos/administración & dosificación , Neuropéptidos/deficiencia , Neuropéptidos/genética , Receptores de Orexina , Orexinas , Ventilación Pulmonar/efectos de los fármacos , Receptores Acoplados a Proteínas G/efectos de los fármacos , Receptores de Neuropéptido/efectos de los fármacos , Reflejo/efectos de los fármacos , Factores de Tiempo , Urea/administración & dosificación , Urea/análogos & derivados , VigiliaRESUMEN
In the appendicular skeleton, substantial evidence demonstrates that somatosensory input from deep tissues including limb muscles and joints elicits somatosympathetic reflexes. Much less is known about the presence and organization of these reflexes from the axial skeleton. We determined if mechanical loading of the lumbar spine and lumbar paraspinal muscle irritation reflexively affects postganglionic sympathetic nerve discharge (SND) to the spleen and kidney. In 27 alpha-chloralose-anesthetized cats, the L2-4 multifidus muscles were injected with the inflammatory irritant mustard oil (20%, 60 microl total) and a vertebral load (100% body weight) was applied dorsal-ventral at the L3 spinous process. Mustard oil injection alone without vertebral loading (n = 7) increased mean splenic SND (60%), renal SND (30%), and heart rate (HR; 52 bpm). Mustard oil injection accompanied by the vertebral load (n = 7) increased mean splenic SND (55%), renal SND (16%), and HR (27 bpm). Blood pressure changes were biphasic and could not account for these changes. When the vertebral load accompanied mustard oil, the increases in splenic SND, renal SND, and HR remained elevated in a pattern significantly different from when the vertebral load was absent. Vehicle injection combined with the mechanical load (n = 3) did not change any of the autonomic responses. Similarly, mustard oil injection combined with a mechanical load did not change these responses when either the medial branches of the dorsal rami from T11-L5 had been cut (n = 4) or when the spinal cord had been transected between the second and third cervical vertebrae (n = 6). The results indicate that inflammatory stimulation of multifidus muscle in the low back evokes a somatosympathetic reflex integrated supraspinally in the upper cervical spinal cord or higher. The reflex's afferent arm travels in the medial branch of the dorsal ramus, and its efferent arm can affect sympathetic outflow to the spleen and the kidney as well as HR and BP. A static mechanical load applied to the lumbar spine accompanying the inflammatory stimulus appears to sustain the inflammatory-induced reflex activity.
Asunto(s)
Anestesia/métodos , Reflejo/fisiología , Médula Espinal/fisiología , Fibras Simpáticas Posganglionares/fisiología , Animales , Gatos , Células Quimiorreceptoras/efectos de los fármacos , Células Quimiorreceptoras/fisiología , Vértebras Lumbares/efectos de los fármacos , Vértebras Lumbares/fisiología , Región Lumbosacra/fisiología , Planta de la Mostaza , Extractos Vegetales/toxicidad , Aceites de Plantas , Reflejo/efectos de los fármacos , Médula Espinal/efectos de los fármacos , Traumatismos de la Médula Espinal/fisiopatología , Fibras Simpáticas Posganglionares/efectos de los fármacos , Soporte de Peso/fisiologíaRESUMEN
Animals can discriminate among many different types of foods. This discrimination process involves multiple sensory systems, but the sense of taste is known to play a central role. We asked how the taste system contributes to the discrimination of different "bitter" taste stimuli in Manduca sexta caterpillars. This insect has approximately eight bilateral pairs of taste cells that respond selectively to bitter taste stimuli. Each bilateral pair of bitter-sensitive taste cells has a different molecular receptive range (MRR); some of these taste cells also contain two signaling pathways with distinctive MRRs and temporal patterns of spiking. To test for discrimination, we habituated the caterpillar's taste-mediated aversive response to one bitter taste stimulus (salicin) and then asked whether this habituation phenomenon generalized to four other bitter taste stimuli (caffeine, aristolochic acid, Grindelia extract, and Canna extract). We inferred that the two compounds were discriminable if the habituation phenomenon failed to generalize (e.g., from salicin to aristolochic acid). We found that M. sexta could discriminate between salicin and those bitter taste stimuli that activate (1) different populations of bitter-sensitive taste cells (Grindelia extract and Canna extract) or (2) different signaling pathways within the same bitter-sensitive taste cell (aristolochic acid). M. sexta could not discriminate between salicin and a bitter taste stimulus that activates the same signaling pathway within the same bitter-sensitive taste cell (caffeine). We propose that the heterogeneous population of bitter-sensitive taste cells and signaling pathways within this insect facilitates the discrimination of bitter taste stimuli.
Asunto(s)
Ácidos Aristolóquicos , Células Quimiorreceptoras/fisiología , Discriminación en Psicología/fisiología , Transducción de Señal/fisiología , Gusto/fisiología , Animales , Alcoholes Bencílicos/farmacología , Cafeína/farmacología , Células Quimiorreceptoras/efectos de los fármacos , Discriminación en Psicología/efectos de los fármacos , Generalización Psicológica/efectos de los fármacos , Generalización Psicológica/fisiología , Glucósidos , Habituación Psicofisiológica/efectos de los fármacos , Habituación Psicofisiológica/fisiología , Larva , Manduca , Fenantrenos/farmacología , Extractos Vegetales/farmacología , Valor Predictivo de las Pruebas , Transducción de Señal/efectos de los fármacos , Estimulación Química , Gusto/efectos de los fármacosRESUMEN
Glucose is an important metabolic factor controlling feeding behavior. There is evidence that physiologically relevant glucose sensors reside in the caudal hindbrain. The area postrema (AP) in particular, which has been characterized as a receptive site for the anorectic hormone amylin, may monitor blood glucose levels. To determine whether glucose and amylin co-activate the same subset of AP neurons, we performed extracellular single unit recordings from a rat AP slice preparation. In 53% of all AP neurons tested (n=32), the activity was positively correlated to the glucose concentration. Interestingly, there was a coincidental sensitivity (94%) of AP neurons to glucose and amylin, which exerted excitatory effects on these cells. We conclude that the co-sensitivity of AP neurons to glucose and amylin, both increasing in response to food intake, points to the AP as an important hindbrain center for the integration of the metabolic and hormonal control of nutrient intake.
Asunto(s)
Amiloide/metabolismo , Regulación del Apetito/fisiología , Células Quimiorreceptoras/metabolismo , Cuarto Ventrículo/metabolismo , Glucosa/metabolismo , Bulbo Raquídeo/metabolismo , Neuronas/metabolismo , Potenciales de Acción/efectos de los fármacos , Potenciales de Acción/fisiología , Amiloide/farmacología , Animales , Regulación del Apetito/efectos de los fármacos , Glucemia/efectos de los fármacos , Glucemia/metabolismo , Células Quimiorreceptoras/citología , Células Quimiorreceptoras/efectos de los fármacos , Interacciones Farmacológicas/fisiología , Cuarto Ventrículo/citología , Cuarto Ventrículo/efectos de los fármacos , Glucosa/farmacología , Hipotálamo/citología , Hipotálamo/efectos de los fármacos , Hipotálamo/metabolismo , Polipéptido Amiloide de los Islotes Pancreáticos , Masculino , Bulbo Raquídeo/citología , Bulbo Raquídeo/efectos de los fármacos , Inhibición Neural/efectos de los fármacos , Inhibición Neural/fisiología , Vías Nerviosas/citología , Vías Nerviosas/efectos de los fármacos , Vías Nerviosas/metabolismo , Neuronas/citología , Neuronas/efectos de los fármacos , Técnicas de Cultivo de Órganos , Ratas , Ratas Wistar , Respuesta de Saciedad/efectos de los fármacos , Respuesta de Saciedad/fisiologíaRESUMEN
The antennules of decapod crustaceans are covered with thousands of chemosensilla that mediate odor discrimination and orientation behaviors. Most studies on chemoreception in decapods have focused on the prominent aesthetasc sensilla. However, previous behavioral studies on lobsters following selective sensillar ablation have revealed that input from nonaesthetasc antennular chemosensilla is sufficient for many odor-mediated behaviors. Our earlier examination of the setal types on the antennules of the Caribbean spiny lobster Panulirus argus revealed three types of nonaesthetasc chemosensilla. The most abundant and widely distributed of these is the hooded sensillum. The present study describes the detailed ultrastructure of antennular hooded sensilla and the physiological response properties of their receptor neurons. Light and scanning and transmission electron microscopy were used to examine structural characteristics, and electrophysiology was used to examine single-unit responses elicited by focal chemical and mechanical stimulation of antennular hooded sensilla. Hooded sensilla have a porous cuticle and are innervated by 9-10 chemosensory and 3 mechanosensory neurons whose dendrites project to the distal end of the sensillum. Hooded sensillar chemosensory neurons responded to waterborne chemicals, were responsive to only one of the six tested single compounds, and had different specificities. Hooded sensillar mechanosensory neurons were not spontaneously active. They had low sensitivity in that they responded to tactile but not waterborne vibrations, and they responded to sensillar deflection with phasic bursts of activity. These results support the idea that hooded sensilla are bimodal chemo-mechanosensilla and are receptors in an antennular chemosensory pathway that parallels the well-described aesthetasc chemosensory pathway.
Asunto(s)
Vías Aferentes/fisiología , Células Quimiorreceptoras/ultraestructura , Mecanorreceptores/ultraestructura , Nephropidae/ultraestructura , Sistema Nervioso/ultraestructura , Neuronas Aferentes/ultraestructura , Olfato/fisiología , Potenciales de Acción/efectos de los fármacos , Potenciales de Acción/fisiología , Adenosina Monofosfato/farmacología , Vías Aferentes/efectos de los fármacos , Aminoácidos/farmacología , Cloruro de Amonio/farmacología , Animales , Células Quimiorreceptoras/efectos de los fármacos , Células Quimiorreceptoras/fisiología , Relación Dosis-Respuesta a Droga , Mecanorreceptores/efectos de los fármacos , Mecanorreceptores/fisiología , Microscopía Electrónica , Microscopía Electrónica de Rastreo , Nephropidae/fisiología , Sistema Nervioso/efectos de los fármacos , Neuronas Aferentes/efectos de los fármacos , Neuronas Aferentes/fisiología , Estimulación Física , Olfato/efectos de los fármacosRESUMEN
A sour taste sensation may be produced when acidic stimuli interact with taste receptor cells (TRCs) on the dorsal surface of the tongue. We have searched for pathways in TRCs that may be activated by acidic stimuli using RT-PCR and changes in intracellular calcium (Ca(2+)(I)) induced by acidic stimuli in rat fungiform papillae. RT-PCR revealed the presence of proton-gated subunits ASIC-beta and VR1. Ca(2+) imaging measurements of the TRCs revealed two distinct responses to acidic stimuli: Ca(2+)(i) was increased in 9% (28/308; Type I) and was decreased in 39% (121/308; Type II). Neither of these responses was affected by the removal of extracellular Ca(2+), indicating that the changes arise from the release and sequestration of Ca(2+) from intracellular stores. These responses were also not inhibited by the vanilloid receptor antagonist, capsazepine, suggesting they do not arise from the activation of vanilloid receptors. The Type I, but not the Type II response was inhibited by amiloride. Dose-response measurements for Types I and II responses yielded pH(50%) of 4.8 and 4.9, respectively. Type II responses were inhibited by pertussis toxin, suggesting G-protein involvement. TRCs that exhibit Type II responses could also be activated by quinine (which increased Ca(2+)(I)) thus suggesting a mechanism by which the addition of acid may be suppressive to other chemical stimuli.
Asunto(s)
Ácidos/farmacología , Capsaicina/análogos & derivados , Proteínas de la Membrana , Proteínas del Tejido Nervioso , Receptores de Droga/metabolismo , Canales de Sodio/metabolismo , Papilas Gustativas/metabolismo , Gusto/fisiología , Canales Iónicos Sensibles al Ácido , Adyuvantes Inmunológicos/farmacología , Amilorida/farmacología , Animales , Calcio/metabolismo , Capsaicina/farmacología , Células Quimiorreceptoras/efectos de los fármacos , Células Quimiorreceptoras/fisiología , Toxina del Cólera/farmacología , Diuréticos/farmacología , Relación Dosis-Respuesta a Droga , Femenino , Proteínas de Unión al GTP/metabolismo , Masculino , Toxina del Pertussis , Protones , Ratas , Ratas Sprague-Dawley , Receptores de Droga/genética , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Canales de Sodio/genética , Estimulación Química , Taquifilaxis/fisiología , Factores de Virulencia de Bordetella/farmacologíaRESUMEN
The aim of this study was to test the hypothesis that capsaicin treatment in lambs selectively inhibits bronchopulmonary C-fiber function but does not alter other vagal pulmonary receptor functions or peripheral and central chemoreceptor functions. Eleven lambs were randomized to receive a subcutaneous injection of either 25 mg/kg capsaicin (6 lambs) or solvent (5 lambs) under general anesthesia. Capsaicin-treated lambs did not demonstrate the classical ventilatory response consistently observed in response to capsaicin bolus intravenous injection in control lambs. Moreover, the ventilatory responses to stimulation of the rapidly adapting pulmonary stretch receptors (intratracheal water instillation) and slowly adapting pulmonary stretch receptors (Hering-Breuer inflation reflex) were similar in both groups of lambs. Finally, the ventilatory responses to various stimuli and depressants of carotid body activity and to central chemoreceptor stimulation (CO(2) rebreathing) were identical in control and capsaicin-treated lambs. We conclude that 25 mg/kg capsaicin treatment in lambs selectively inhibits bronchopulmonary C-fiber function without significantly affecting the other vagal pulmonary receptor functions or that of peripheral and central chemoreceptors.
Asunto(s)
Capsaicina/farmacología , Células Quimiorreceptoras/efectos de los fármacos , Pulmón/inervación , Pulmón/fisiología , Reflejo/efectos de los fármacos , Nervio Vago/fisiología , Factores de Edad , Animales , Animales Recién Nacidos , Apnea/inducido químicamente , Apnea/fisiopatología , Células Quimiorreceptoras/fisiología , Hipoxia/inducido químicamente , Hipoxia/fisiopatología , Mecanorreceptores/efectos de los fármacos , Mecanorreceptores/fisiología , Fibras Nerviosas/efectos de los fármacos , Fibras Nerviosas/fisiología , Reflejo/fisiología , Pruebas de Función Respiratoria , Mecánica Respiratoria/efectos de los fármacos , Mecánica Respiratoria/fisiología , Ovinos , Nervio Vago/efectos de los fármacosRESUMEN
Feeding and blood glucose responses to local injection of nanoliter volumes of 5-thio-D-glucose (5TG), a potent antimetabolic glucose analogue, were studied at 142 hindbrain and 61 hypothalamic cannula sites. A site was considered positive if 5TG elicited at least 1.5 g more food intake or a hyperglycemic response at least 25 mg/dl greater than the respective responses elicited by vehicle injection in the same rat. Of 61 hypothalamic cannula sites tested, none were positive for blood glucose and only one was positive for feeding. Increasing the 5TG dose to 48 ug did not produce additional positive results at hypothalamic sites. In contrast, 66 hindbrain sites were positive for feeding and 49 were positive for blood glucose, with 33 of these being positive for both responses. The distribution of positive sites for feeding and hyperglycemia overlapped almost completely. Positive sites were concentrated in two distinct zones: one in the ventrolateral and one in the dorsomedial medulla. In both locations, the glucoreceptive areas extended approximately from the level of the area postrema (AP) to the pontomedullary junction. Glucoreceptive zones were co-distributed with epinephrine cell groups C1-C3, suggesting that epinephrine neurons may be important components of the neural circuitry for glucoregulation. Localization of glucoreceptive sites will facilitate positive identification of glucoreceptor cells and the direct analysis of the neural mechanisms through which they influence food intake and metabolic responses.
Asunto(s)
Glucemia/metabolismo , Conducta Alimentaria/fisiología , Glucosa/análogos & derivados , Hipotálamo/fisiología , Receptores de Superficie Celular/fisiología , Rombencéfalo/fisiología , Animales , Antimetabolitos/farmacología , Glucemia/efectos de los fármacos , Mapeo Encefálico , Células Quimiorreceptoras/efectos de los fármacos , Células Quimiorreceptoras/fisiología , Ingestión de Energía/efectos de los fármacos , Ingestión de Energía/fisiología , Conducta Alimentaria/efectos de los fármacos , Femenino , Glucosa/administración & dosificación , Glucosa/farmacología , Hipotálamo/efectos de los fármacos , Masculino , Microinyecciones , Ratas , Ratas Sprague-Dawley , Receptores de Superficie Celular/efectos de los fármacos , Rombencéfalo/efectos de los fármacosRESUMEN
We postulated that dose-responsive satiety after oil premeals varies with the number of gut sensors stimulated by lipolytic products along intestine. These experiments in fasted rats on satiety after oil premeals were performed to 1) determine whether satiety was induced by lipolytic products but not triglycerides; 2) confirm that oil empties from the stomach at rates that vary with oil loads; 3) ascertain that increasing rates of oil entry into duodenum extend the length of gut contacted by lipolytic products; and 4) judge whether length of gut contacted correlated with dose-responsive satieties to dietary oils. 5) Using specific antagonists, we attempted to define how satiety was signalled by gut sensors. Timing and degrees of satiety did not correlate with timing and extent of gastric distensions but, rather, with the timing and extent of spread of lipolytic products along small bowel. Satiety after the highest premeal load of oil was blocked by Pluronic L-81, an inhibitor of intestinal secretion of apolipoprotein A-IV, but was unaffected by MK-329 (a specific antagonist of cholecystokinin) or by capsaicin blockade of chemosensory nerves.
Asunto(s)
Aceite de Maíz/farmacología , Grasas de la Dieta , Ingestión de Alimentos/fisiología , Intestino Delgado/fisiología , Respuesta de Saciedad/fisiología , Análisis de Varianza , Animales , Radioisótopos de Carbono , Células Quimiorreceptoras/efectos de los fármacos , Células Quimiorreceptoras/fisiología , Colecistoquinina/antagonistas & inhibidores , Devazepida/farmacología , Ayuno , Ácidos Grasos no Esterificados/metabolismo , Glucanos/farmacología , Absorción Intestinal , Lipólisis , Masculino , Modelos Biológicos , Poloxámero/farmacología , Ratas , Ratas Sprague-Dawley , Respuesta de Saciedad/efectos de los fármacos , Factores de Tiempo , Trioleína/metabolismo , TritioRESUMEN
In urethane-anaesthetized rats, stimulation of carotid body chemoreceptors desynchronizes the cortical electroencephalogram and increases the sensitivity of thalamic and cortical somatosensory neurones to peripheral sensory nerve stimulation. Peripheral chemoreceptors were stimulated by injecting a bolus (30 ml) or infusing 100 ml of 0.18 M NaCl solution equilibrated with 100% CO2 into an internal carotid artery, the cortical electroencephalogram and ventilation were monitored routinely. This stimulus induced hyperventilation and desynchronization of the cortical electroencephalogram. Anaesthetized rats also showed spontaneous periodic increases in ventilation rate accompanied by changes of the cortical electroencephalogram from high-voltage low frequency to low-voltage high frequency which seemed to be identical with those evoked by stimulating chemoreceptors. The activity of identified somatosensory neurons in the thalamic ventrobasal complex, layer IV of the somatosensory cortex, or the cuneate nucleus was recorded extracellularly during and following chemoreceptor activation. Neurones in the ventrobasal thalamus and somatosensory cortex showed a decrease in latency and an increase in probability of discharge to supramaximal electrical stimulation of the forepaw which was more pronounced following infusion stimulation of the carotid body than following bolus stimulation. In contrast, neurons within the cuneate nucleus showed a slight increase in latency to onset and a decrease in the probability of firing following the same stimulus. The results indicate that stimulation of the carotid body chemoreceptors leads to an enhancement of the response of somatosensory neurons to their normal physiological input.
Asunto(s)
Encéfalo/fisiología , Cuerpo Carotídeo/fisiología , Células Quimiorreceptoras/fisiología , Neuronas/fisiología , Corteza Somatosensorial/fisiología , Tálamo/fisiología , Anestésicos Intravenosos , Animales , Dióxido de Carbono/sangre , Dióxido de Carbono/farmacología , Arteria Carótida Interna , Corteza Cerebral/fisiología , Células Quimiorreceptoras/efectos de los fármacos , Estimulación Eléctrica , Electroencefalografía/efectos de los fármacos , Femenino , Miembro Anterior , Ratas , Ratas Endogámicas , Respiración/efectos de los fármacos , Respiración/fisiología , Piel/inervación , UretanoRESUMEN
A subset of olfactory receptor neurons of the Caribbean spiny lobster Panulirus argus possesses receptors for L-glutamate that can mediate both excitatory and inhibitory responses (P.C. Daniel, M.F. Burgess, C.D. Derby, Responses of olfactory receptor neurons in the spiny lobster to binary mixtures are predictable using a non-competitive model that incorporates excitatory and inhibitory transduction pathways, J. Comp. Physiol. A 178 (1992) 523-536). In this study, we have used biochemical and electrophysiological techniques to understand the role of these receptors in olfactory transduction, and to compare these olfactory glutamate receptors with peripheral and central L-glutamate receptors in other animals. Using a radioligand-binding assay with a membrane-rich preparation from the dendrites of olfactory receptor neurons, we have identified two types of binding sites for L-glutamate. Both sites showed rapid, reversible, and saturable association with radiolabeled L-glutamate, and their Kd values (1 nM and 3 microM) are effective in physiological studies of glutamate-sensitive olfactory neurons, suggesting these binding sites are receptors involved in olfactory transduction. Both sites were completely inhibited by high concentrations of NMDA and L-cysteine, and only partially inhibited by other L-glutamate analogs and odorants. Electrophysiological recordings from L-glutamate-best olfactory receptor neurons showed that NMDA and L-cysteine are both partial agonists and antagonists of glutamate receptors. Together, these results suggest the olfactory L-glutamate receptors of spiny lobsters are novel types of L-glutamate receptors that are functionally important in mediating olfactory responses.
Asunto(s)
Células Quimiorreceptoras/fisiología , Cisteína/metabolismo , Nephropidae/fisiología , Receptores de Glutamato/fisiología , Receptores de N-Metil-D-Aspartato/metabolismo , Olfato/fisiología , Animales , Células Quimiorreceptoras/efectos de los fármacos , Electrofisiología , Agonistas de Aminoácidos Excitadores/farmacología , Antagonistas de Aminoácidos Excitadores/farmacología , Espacio Extracelular/fisiología , Ácido Glutámico/farmacología , Cinética , Odorantes , Ensayo de Unión Radioligante , Receptores de N-Metil-D-Aspartato/agonistas , Receptores de N-Metil-D-Aspartato/antagonistas & inhibidores , Olfato/efectos de los fármacos , Estimulación QuímicaRESUMEN
When compared to patients with erosive esophagitis, patients with Barrett's esophagus have demonstrated reduced chemo- and mechanoreceptor sensitivity to acid infusion and balloon distension, respectively. However, anecdotal clinical experience suggested an increase in symptom perception in patients after successful elimination of Barrett's epithelium, using multipolar electrocoagulation (MPEC) and high-dose proton pump inhibitor (PPI). To determine perception thresholds to acid infusion, we evaluated eight consecutive patients after a series of MPEC treatments resulted in complete elimination of Barrett's mucosa and compared them to 10 age-matched patients with nonreversed Barrett's esophagus and 10 patients with symptomatic, endoscopy-documented erosive esophagitis (Hetzel-Dent grade 2 or greater). Chemosensitivity was determined by a modified acid perfusion test, where acid perception thresholds were quantified by the lag time to initial typical symptom perception, sensory intensity rating, and an acid perfusion sensory score (APSS). While patients after successful elimination of Barrett's esophagus had similar sensory intensity ratings and APSS as patients with erosive esophagitis, the lag times differed significantly between the groups, and both groups had significantly higher sensory intensity ratings and APSS than patients with nonreversed Barrett's esophagus. In conclusion, patients after complete reversal of Barrett's mucosa are unexpectedly as sensitive to acid as symptomatic patients with erosive esophagitis.
Asunto(s)
Esófago de Barrett/terapia , Células Quimiorreceptoras/efectos de los fármacos , Esofagitis Péptica/diagnóstico , Esófago/efectos de los fármacos , Antiulcerosos/uso terapéutico , Esófago de Barrett/diagnóstico , Esófago de Barrett/fisiopatología , Estudios de Casos y Controles , Células Quimiorreceptoras/fisiopatología , Terapia Combinada , Electrocoagulación , Esofagitis Péptica/fisiopatología , Esófago/fisiopatología , Femenino , Humanos , Ácido Clorhídrico , Masculino , Persona de Mediana Edad , Omeprazol/uso terapéutico , Inhibidores de la Bomba de Protones , Umbral Sensorial/fisiologíaRESUMEN
The aim of our paper was to investigate whether single olfactory receptor neurons (ORNs) of the spiny lobster Panulirus argus functionally express more than one type of receptor, examine the consequences of this on coding of mixtures, and compare principles of odorant mixture coding by spiny lobsters with that by the channel catfish, which has been studied extensively using the same experimental and analytical procedures (Caprio et al. 1989; Kang and Caprio 1991). We examined responses of individual taurine-sensitive ORNs to binary mixtures of excitatory compounds, either competitive agonists (taurine, beta-alanine, hypotaurine) or non-competitive agonists (taurine, L-glutamate, ammonium chloride, adenosine-5'-monophosphate). Responses to mixtures were compared to two indices: mixture discrimination index (MDI) and independent component index (ICI). Binary mixtures of competitive agonists had MDI values close to 1.0, as expected for competitors. Mixtures of non-competitive agonists had ICI values averaging 0.83, indicating the effects of the components are not independent. We conclude that individual olfactory cells of spiny lobsters can express more than one type of receptor mediating excitation, one of which typically has a much higher density or affinity, and that spiny lobster and catfish olfactory cells encode mixtures of two excitatory agonists using similar rules.