A subpopulation of large neurons of the sympathetic superior cervical ganglion innervates the NGF-rich submandibular salivary gland in young adult and aged mice

1995 ◽  
Vol 50 (3) ◽  
pp. 283-289 ◽  
Author(s):  
Sirkka Lahtivirta ◽  
Jari Koistinaho ◽  
Antti Hervonen
1962 ◽  
Vol 202 (3) ◽  
pp. 425-428 ◽  
Author(s):  
Herbert Wells

Administration of isoproterenol, like amputation of lower incisor teeth, resulted in a marked increase in both the fresh and dry weights of the submandibular salivary glands of rats. There was a linear relationship between the percent increase in gland weight and the dose of isoproterenol between 10 and 160 mg/kg/day. Ten days after cessation of isoproterenol administration, the weight of the enlarged glands had receded to control levels. Although prior unilateral extirpation of the superior cervical ganglion inhibited the response to incisor amputation of the submandibular gland on the operated side, both glands enlarged to the same extent following administration of isoproterenol. When isoproterenol administration was combined with amputation of the incisors, the effects on gland weight were additive.


2011 ◽  
Vol 500 (1) ◽  
pp. 57-62 ◽  
Author(s):  
Joanna Wojtkiewicz ◽  
Judyta K. Juranek ◽  
Ireneusz Kowalski ◽  
Marek Bladowski ◽  
Jarosław Całka ◽  
...  

2019 ◽  
Vol 98 (10) ◽  
pp. 1122-1130 ◽  
Author(s):  
T.H.N. Teshima ◽  
A.S. Tucker ◽  
S.V. Lourenço

Neuronal signaling is known to be required for salivary gland development, with parasympathetic nerves interacting with the surrounding tissues from early stages to maintain a progenitor cell population and control morphogenesis. In contrast, postganglionic sympathetic nerves arrive late in salivary gland development to perform a secretory function; however, no previous report has shown their role during development. Here, we show that a subset of neuronal cells within the parasympathetic submandibular ganglion (PSG) express the catecholaminergic marker tyrosine hydroxylase (TH) in developing murine and human submandibular glands. This sympathetic phenotype coincided with the expression of transcription factor Hand2 within the PSG from the bud stage (E12.5) of mouse embryonic salivary gland development. Hand2 was previously associated with the decision of neural crest cells to become sympathetic in other systems, suggesting a role in controlling neuronal fate in the salivary gland. The PSG therefore provides a population of TH-expressing neurons prior to the arrival of the postganglionic sympathetic axons from the superior cervical ganglion at E15.5. In culture, in the absence of nerves from the superior cervical ganglion, these PSG-derived TH neurons were clearly evident forming a network around the gland. Chemical ablation of dopamine receptors in explant culture with the neurotoxin 6-hydroxydopamine at early stages of gland development resulted in specific loss of the TH-positive neurons from the PSG, and subsequent branching was inhibited. Taken altogether, these results highlight for the first time the detailed developmental time course of TH-expressing neurons during murine salivary gland development and suggest a role for these neurons in branching morphogenesis.


Author(s):  
D. M. DePace

The majority of blood vessels in the superior cervical ganglion possess a continuous endothelium with tight junctions. These same features have been associated with the blood brain barrier of the central nervous system and peripheral nerves. These vessels may perform a barrier function between the capillary circulation and the superior cervical ganglion. The permeability of the blood vessels in the superior cervical ganglion of the rat was tested by intravenous injection of horseradish peroxidase (HRP). Three experimental groups of four animals each were given intravenous HRP (Sigma Type II) in a dosage of.08 to.15 mg/gm body weight in.5 ml of.85% saline. The animals were sacrificed at five, ten or 15 minutes following administration of the tracer. Superior cervical ganglia were quickly removed and fixed by immersion in 2.5% glutaraldehyde in Sorenson's.1M phosphate buffer, pH 7.4. Three control animals received,5ml of saline without HRP. These were sacrificed on the same time schedule. Tissues from experimental and control animals were reacted for peroxidase activity and then processed for routine transmission electron microscopy.


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