PubMed · 8800751
The source did not provide an abstract. Follow the original record for more information.
Explore connections, maps & timelines
1996-01-05. Special issue: Interoception and behavior.. https://pubmed.ncbi.nlm.nih.gov/8800751/
Cite the original work for its findings. Save a collection to share your selection of sources.
KEEP EXPLORING
1. Cardiac vagal receptors are chemically and/or mechanically sensitive but it is unknown if this information is preserved centrally within the nucleus of the solitary tract (NTS). The present study had two aims: first, to investigate qualitatively whether both mechanically and chemically sensitive cardiac vagal encoding were preserved within the NTS, and second, to determine the patterns of convergence from other cardiorespiratory afferents to NTS neurones receiving cardiac vagal inputs. 2. The extracellular activity of single NTS neurones was investigated during stimulation of both chemically and mechanically sensitive cardiac vagal receptors in a working heart-brainstem preparation of mouse. Chemically sensitive cardiac receptors were stimulated using intra-left ventricular injections of either veratridine (1-3 microg kg-1), bradykinin (0.25-1 microg) or prostaglandin E2 (100-200 ng), whereas the left ventricle was distended to activate cardiac mechanoreceptors. 3. Forty-three NTS neurones were activated both synaptically by electrical stimulation of the ipsilateral vagus nerve (latency, 35 +/- 3 ms), and by intra-left ventricular injection of veratridine and also, in some cases, by bradykinin and/or PGE2. These NTS neurones were delineated into two populations based on their response to left ventricular distension and convergence properties. Left ventricular distension-insensitive neurones (n = 30) were excited by stimulation of carotid body chemoreceptors (81 %) but not arterial baroreceptors (3 %; i.e. n = 1 neurone), whereas distension-sensitive cells (n = 13) were activated mainly by baroreceptors (86 %) rather than peripheral chemoreceptors (14 %; i.e. n = 1 neurone). 4. The data reveal two distinct populations of NTS neurones receiving cardiac vagal inputs: (a) cells responsive to veratridine stimulation only, and (b) neurones activated by both veratridine and mechanical stimuli. The specific convergence pattern of baroreceptors and chemoreceptors to these cardioreceptive NTS neurones is discussed in relation to a common afferent modality integration within the NTS.
Central projections of nerves innervating the rabbit maxillary sinus were localized by using wheat germ agglutinin-horseradish peroxidase (WGA-HRP) or choleragenoid-horseradish peroxidase (B-HRP). Tracer was placed into the left maxillary sinus; rabbits were killed 3 or 5 days later, and histochemical localization of transported WGA-HRP or B-HRP was performed. Labeled cell bodies (437-545/animal) were seen in the ipsilateral trigeminal ganglion. Very few labeled cell bodies (zero to three/animal) were observed in the contralateral ganglion. The area of cell bodies labeled by WGA-HRP appeared similar to the area of cell bodies labeled by B-HRP. Transganglionic projections from either tracer were localized to lamina II of the ipsilateral subnucleus caudalis. In addition, WGA-HRP labeling was occasionally observed in lamina I. No labeling was present in other areas of the brainstem. In contrast to the above results, other studies have demonstrated that B-HRP produces terminal-like labeling in deeper layers of the gray matter. We injected B-HRP into the infraorbital nerve and sciatic nerve, which are known to contain projections to deep layers of the gray matter. Labeling was observed in the deep layers of the medullary or spinal dorsal horn 5 days later, suggesting that nerves innervating the sinus only project to superficial laminae. These results suggest that neurons in superficial laminae of the subnucleus caudalis may be important for the reflex initiation of the increased glandular secretions in the maxillary sinus during sinusitis.
It has been postulated that, in the adult visual cortex, visual inputs modulate levels of mRNAs coding for neurotransmitter receptors in an activity-dependent manner. To investigate this possibility, we performed a monocular enucleation in adult rabbits and, 15 days later, collected their left and right visual cortices. Levels of mRNAs coding for voltage-activated sodium channels, and for receptors for kainate/alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA), N-methyl-D-aspartate (NMDA), gamma-aminobutyric acid (GABA), and glycine were semiquantitatively estimated in the visual cortices ipsilateral and contralateral to the lesion by the Xenopus oocyte/voltage-clamp expression system. This technique also allowed us to study some of the pharmacological and physiological properties of the channels and receptors expressed in the oocytes. In cells injected with mRNA from left or right cortices of monocularly enucleated and control animals, the amplitudes of currents elicited by kainate or AMPA, which reflect the abundance of mRNAs coding for kainate and AMPA receptors, were similar. There was no difference in the sensitivity to kainate and in the voltage dependence of the kainate response. Responses mediated by NMDA, GABA, and glycine were unaffected by monocular enucleation. Sodium channel peak currents, activation, steady-state inactivation, and sensitivity to tetrodotoxin also remained unchanged after the enucleation. Our data show that mRNAs for major neurotransmitter receptors and ion channels in the adult rabbit visual cortex are not obviously modified by monocular deafferentiation. Thus, our results do not support the idea of a widespread dynamic modulation of mRNAs coding for receptors and ion channels by visual activity in the rabbit visual system.