scholarly journals Subdiaphragmatic Vagotomy v1 (protocols.io.bfhdjj26)

protocols.io ◽  
2020 ◽  
Author(s):  
Kavi Rude ◽  
Jessica Sladek ◽  
Colin Reardon
1981 ◽  
Vol 27 (3) ◽  
pp. 523-527 ◽  
Author(s):  
B KING ◽  
G PHELPS ◽  
L FROHMAN

2001 ◽  
Vol 280 (4) ◽  
pp. R929-R934 ◽  
Author(s):  
Michael K. Hansen ◽  
Kevin A. O'Connor ◽  
Lisa E. Goehler ◽  
Linda R. Watkins ◽  
Steven F. Maier

It has been suggested that proinflammatory cytokines communicate to the brain via a neural pathway involving activation of vagal afferents by interleukin-1β (IL-1β), in addition to blood-borne routes. In support, subdiaphragmatic vagotomy blocks IL-1β-induced, brain-mediated responses such as fever. However, vagotomy has also been reported to be ineffective. Neural signaling would be expected to be especially important at low doses of cytokine, when local actions could occur, but only very small quantities of cytokine would become systemic. Here, we examined core body temperature after intraperitoneal injections of three doses of recombinat human IL-1β (rh-IL-1β). Subdiaphragmatic vagotomy completely blocked the fever produced by 0.1 μg/kg, only partially blocked the fever produced by 0.5 μg/kg, and had no effect at all on the fever that followed 1.0 μg/kg rh-IL-1β. Blood levels of rh-IL-1β did not become greater than normal basal levels of endogenous rat IL-β until the 0.5-μg/kg dose nor was IL-1β induced in the pituitary until this dose. These results suggest that low doses of intraperitoneal IL-1β induce fever via a vagal route and that dose may account for some of the discrepancies in the literature.


2005 ◽  
Vol 168 (1-2) ◽  
pp. 83-95 ◽  
Author(s):  
Christine Linard ◽  
Christel Marquette ◽  
Didier Clarençon ◽  
Monique Galonnier ◽  
Jacques Mathieu ◽  
...  

Synapse ◽  
2011 ◽  
Vol 66 (2) ◽  
pp. 95-105 ◽  
Author(s):  
Sadayoshi Furuta ◽  
Lisa Watanabe ◽  
Seira Doi ◽  
Hiroshi Horiuchi ◽  
Kenjiro Matsumoto ◽  
...  

1999 ◽  
Vol 276 (5) ◽  
pp. R1276-R1288 ◽  
Author(s):  
Wesley White ◽  
Gary J. Schwartz ◽  
Timothy H. Moran

Within a feeding schedule of intermittent food access, large meals have the ability to induce activity at the same time the next day [circadian ensuing activity (CEA)]. In these experiments, we evaluated the minimum meal size necessary to induce CEA and whether oral-pharyngeal factors and afferent vagal activity played necessary roles in the induction of the underlying process. In experiment 1, every 33 h rats were given two meals separated by a 2-h interval. The size of the first meal was varied, while total intake every feeding cycle was held constant. When the initial meal was <10 g (34 kcal) CEA occurred later, indicating that such a meal size was subthreshold for inducing CEA. In experiment 2, rats were given intragastric (IG) meals every 33 h, before and after complete subdiaphragmatic vagotomy. IG nutrient meals induced CEA, indicating that extensive oral-pharyngeal experience was not necessary for CEA induction. CEA occurred in vagotomized rats but, compared with intact rats, appeared to occur later relative to nutrient infusion, indicating that afferent vagal activity may be sufficient but not necessary to induce CEA.


1985 ◽  
Vol 249 (3) ◽  
pp. E239-E243 ◽  
Author(s):  
P. L. Andrews ◽  
N. J. Rothwell ◽  
M. J. Stock

Infusion of rats with insulin (8 U/day via implanted minipump) for 7 days caused a 22% rise in resting oxygen consumption, which was inhibited by acute injection of the beta-adrenergic antagonist propranolol. Insulin treatment produced significant increases in brown fat mass, protein content, and total thermogenic activity (assessed from binding of guanosine diphosphate to isolated brown fat mitochondria), but these responses were inhibited by prior surgical sympathectomy of the tissue. Animals subjected to subdiaphragmatic vagotomy gained more weight than pair-fed, sham-operated controls and showed reductions in total energy expenditure, the acute thermogenic response to a meal and brown adipose tissue activity. Daily injections of insulin (1 U/day) prevented all of these effects of vagotomy. These data demonstrate that the changes in brown fat activity induced by exogenous insulin are mediated by the sympathetic nervous system and that the depressed thermogenesis and brown fat activity associated with vagotomy appear to be due to a relative insulin deficiency and can be reversed by treatment with the hormone.


Sign in / Sign up

Export Citation Format

Share Document