Plasma constituents and mortality in rat pups given chronic insulin via injection, pellet, or osmotic minipump

2002 ◽  
Vol 80 (3) ◽  
pp. 180-192 ◽  
Author(s):  
Carl I Thompson ◽  
John W Munford ◽  
Edward H Buell ◽  
Robert J Karry ◽  
Charles T Lee ◽  
...  

Two studies compared the glucose responses of 9-day-old rats given subcutaneous insulin, either continuously or via daily injection, for 10 days. In Experiment 1, implanted pellets released a total of 0, 1.9, or 5.7 U insulin/kg the first 24 h. Injected doses were larger, 0 or 8 U/kg. Injections caused no deaths, but insulin-releasing pellets caused high mortality within 24 h. Pups surviving the pellets were normoglycemic by treatment day 8. In Experiment 2, pups received 0.184 U of insulin daily, approximately 8 U/kg at 9 days, via either injection or osmotic minipump. All pups survived. Injected pups were hypoglycemic 2 h postinjection through treatment day 10, whereas pups with insulin minipumps were normoglycemic by day 5. Insulin injections, but not minipumps, lowered plasma triglycerides on day 10. To examine age differences in response to insulin, additional pups and adults received daily injections of 0 or 8 U/kg for 10 days. All survived. Insulin lowered plasma glucose more in pups than in adults and reduced triglycerides in pups but not in adults. The rapid development of normoglycemia in pups with insulin minipumps, compared with pups injected daily with the same dose, suggests that continuous early insulin may produce insulin resistance.Key words: route of insulin administration, insulin resistance, mortality, plasma glucose, development.

2021 ◽  
Vol 23 (1) ◽  
pp. 35-38
Author(s):  
L. I. Bon ◽  
◽  
S. M. Zimatkin ◽  

The aim of this work was to study the ultrastructure of the internal pyramidal neurons of the neocortex of 5-day-old rat pups after antenatal alcoholization. The studies were carried out on female outbred white rats with an initial weight of 230 ± 20 g and their offspring. Prenatal alcoholization causes deep and varied ultrastructural changes in pyramidal neurons in the neocortex of 5-day-old rats. Moreover, these violations of direct action not only as a consequence of the damaging effect of alcohol, its metabolite acetehyde or the oxidative stress they cause on the membranes and organelles of neurons during embryogenesis, but also as a violation of the normal "program" of development" of neurons in the cortex.


1986 ◽  
Vol 250 (2) ◽  
pp. G200-G204 ◽  
Author(s):  
J. Yahav ◽  
P. C. Lee ◽  
E. Lebenthal

By use of isolated gastric glands from rats at various ages, we demonstrated that full-term neonate and 1-day-old rats showed no response to cholecystokinin octapeptide (CCK-OP), carbachol, or Ca2+ ionophore. The same glands, however, were responsive to dibutyryl cAMP. A mature response was not found until the pups were 2 days old. Injection of hydrocortisone into newborn rats led to an increase in pepsinogen concentrations in gastric glands and also an increased responsiveness to CCK-OP, carbachol, and Ca2+ ionophore A23187 24 h after administration. Hydrocortisone thus caused precocious maturation of both pepsinogen accumulation and pepsinogen secretory responsiveness of gastric glands in rat pups.


1988 ◽  
Vol 255 (6) ◽  
pp. R901-R907 ◽  
Author(s):  
A. Weller ◽  
E. M. Blass

In adult mammals, cholecystokinin (CCK)-opiate interactions are complex and task dependent. Specifically, CCK antagonizes opiate effects in some cases, yet acts similarly to opiate agonists in others. The present study used behavioral measures to determine how CCK interacts with opiates in neonatal rats. CCK, at doses of 1 microgram/kg and higher, markedly reduced isolation-induced distress vocalization in rat pups. Moreover, CCK selectively prevented naltrexone antagonism of opiate-mediated reduction in distress vocalization in 3- and 11-day-old rats. Yet CCK did not affect opiate-induced analgesia, as measured by the hot-plate paw-lift response. Thus CCK either did not interact with opiates or did so agonistically, with the same (low) dose range, and within subjects. These findings suggest independence of stress and pain systems in neonatal rats and demonstrate a functional interaction between CCK and opioid systems.


1999 ◽  
Vol 18 (3) ◽  
pp. 174-179 ◽  
Author(s):  
Alka Gupta ◽  
Renu Agarwal ◽  
Girja S Shukla

1 The effect of certain pesticides on the functional integrity of the developing blood-brain barrier (BBB) was studied following single and repeated exposure, and after subsequent withdrawal in rats. 2 Ten-day-old rat pups exposed orally to quinalphos (QP, organophosphate), cypermethrin (CM, pyre-throid) and lindane (LD, organochlorine) at a dose of 1/50th of LD50, showed a significant increase in the brain uptake index (BUI) for a micromolecular tracer, sodium fluorescein (SF), by 97, 37 and 72%, respectively, after 2 h. Residual increases in the BUI were found even after 3 days of the single treatment of QP (28%) and LD (23%). 3 Repeated exposure for 8 days (postnatal days (PND) 10-17) with QP, CM and LD increased the BBB permeability by 130, 80 and 50%, respectively. Recovery from these changes was complete in QP and LD-treated animals after 13 days (PND 18-30) of withdrawal. However, CM showed persistent effects that were normalized only after 43 days (PND 18-60) of withdrawal. 4 A single dose reduced to 1/100th of LD50 also increased BUI in 10-day-old rat pups following QP (20%) and CM (28%) exposure at 2 h. 5 An age-dependent effect of these pesticides was evident from the study showing higher magnitude of BUI changes in 10-day-old rats as compared to that in 15- day-old rats. Furthermore, adult rats did not show any effect on BBB permeability even at a higher dose (1/25th of LD50) of these pesticides given alone or in combination with piperonyl butoxide (600 mg/kg, i.p.) for 3 consecutive days. 6 This study showed that developing BBB is highly vulnerable to single or repeated exposure of certain pesticides. The observed persistent effects during brain development even after withdrawal of the treatment may produce some neurological dysfunction at later life as well.


1993 ◽  
Vol 265 (2) ◽  
pp. G354-G360 ◽  
Author(s):  
B. L. Tepperman ◽  
B. L. Vozzolo ◽  
B. D. Soper

Epidermal growth factor (EGF) originating from salivary glands has been shown to affect the development and integrity of rodent gastrointestinal mucosa. Because newborn rats receive EGF from maternal milk, we have examined the effect of sialoadenectomy as a method of depleting EGF in milk on the resistance of neonatal rat mucosa to luminal H+. Rat dams were sialoadenectomized (SALX) or sham operated 5 days after parturition. Experiments were performed on newborns 10-22 days old. Mucosal permeability responses to intraluminal HCl (300 mM) were examined in terms of luminal appearances of Na+, K+, and protein and H+ loss. EGF levels in maternal milk were determined by immunoassay. In rat pups from control litters, luminal HCl resulted in an age-associated increase in cation and protein flux across the gastric mucosa. Luminal cation and protein fluxes observed in 10- to 18-day-old rat pups from SALX dams were not significantly different from similarly aged rats from control dams. However, in 19- to 22-day-old rats from SALX dams, the permeability responses to luminal HCl were exacerbated compared with similarly aged neonates from control dams. These responses were reduced by treatment with EGF. EGF levels in milk from sham-operated and SALX dams were not significantly different in the 10- to 16-day lactational period. However, in SALX dams EGF was significantly reduced at 19 and 22 days. Chromatographic elution pattern of milk EGF was dissimilar to the pattern exhibited by submandibular gland EGF.(ABSTRACT TRUNCATED AT 250 WORDS)


1981 ◽  
Vol 2 (1_suppl) ◽  
pp. 27-29 ◽  
Author(s):  
Janet M. Roscoe

A review of protocols for the administration of insulin in diabetics during CAPD in the various Toronto hospitals and from two other centers outside Canada show that they are similar but not identical. Toronto Western Hospital, Iowa Lutheran Hospital, Pitie-Salpetriere Hospital and Sunnybrook Medical Center use intraperitoneal insulin exclusively. Toronto General Hospital and the Wellesley Hospital used a combination of intraperitoneal and subcutaneous insulin. Most patients performed four exchanges daily, although some did three only. Nighttime insulin was reduced in most patients. Average insulin requirements were higher when given by intraperitoneal as opposed to subcutaneous injection. There was insufficient data to compare the control achieved with each protocol.


Metabolism ◽  
1990 ◽  
Vol 39 (6) ◽  
pp. 598-604 ◽  
Author(s):  
Giacomo Ruotolo ◽  
Piero Micossi ◽  
Gabriella Galimberti ◽  
Maria Cristina Librenti ◽  
Giovanna Petrella ◽  
...  

2013 ◽  
Vol 46 (20) ◽  
pp. 524-529 ◽  
Author(s):  
P. Palumbo ◽  
P. Pepe ◽  
J.D. Kong ◽  
S.S. Kumar ◽  
S. Panunzi ◽  
...  

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