Literature DB >> 7315972

Transport of calcium by duodenum of spontaneously hypertensive rat.

M A Toraason, G L Wright.   

Abstract

The absorption of calcium by segments of duodenum obtained from spontaneously hypertensive (SH) rats and normotensive Wistar-Kyoto (WKy) rats was measured before and after the development of hypertension. The systolic blood pressure (SBP) of 5-wk-old SH rats (116 +/- 4 Torr) was significantly elevated above that of age-matched WKy rats (103 +/- 3 Torr) but was not at a level generally considered to be hypertensive. Values obtained for calcium transport [ratio of serosal-to-mucosal fluid 45Ca2+ concn (S/M ratio)] from everted duodenal sacs were similar between the two groups at this age. At 12 wk of age, SH rats exhibited a SBP (153 +/- 4 Torr) well above that of WKy controls (127 +/- 3 Torr), and calcium S/M ratios for duodenal sacs were significantly greater than the WKy control values. Similarly, the in vivo uptake of calcium in duodenal segments was significantly elevated in 12-wk-old SH rats compared with WKy controls. The administration of vitamin D3 or its metabolite, 25-hydroxycholecalciferol, had no detectable effect on duodenal transport of calcium in 12-wk-old SH or WKy rats. By comparison, 1,25-dihydroxycholecalciferol produced a significant increase in duodenal calcium transport both in vitro and in vivo in WKy but not in SH rats. The results indicate a distinct abnormality in the transport of calcium in the duodenum of SH rats, suggesting that the decrease in duodenal uptake of calcium that normally occurs with maturation is slow to develop in this rat strain.

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Year:  1981        PMID: 7315972     DOI: 10.1152/ajpgi.1981.241.4.G344

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  8 in total

1.  Atrial natriuretic peptide is eliminated from the brain by natriuretic peptide receptor-C-mediated brain-to-blood efflux transport at the blood-brain barrier.

Authors:  Shingo Ito; Sumio Ohtsuki; Yuki Katsukura; Miho Funaki; Yusuke Koitabashi; Akihiko Sugino; Sho Murata; Tetsuya Terasaki
Journal:  J Cereb Blood Flow Metab       Date:  2010-07-14       Impact factor: 6.200

2.  Impaired duodenal response to short-term dietary calcium restriction in adolescent spontaneously hypertensive rats.

Authors:  S Chabanis; P Duchambon; H Banide; P Aymard; B Lacour; T Drüeke
Journal:  Calcif Tissue Int       Date:  1993-04       Impact factor: 4.333

3.  Increased calcium absorption in prehypertensive spontaneously hypertensive rat. Role of serum 1,25-dihydroxyvitamin D3 levels and intestinal brush border membrane fluidity.

Authors:  K Lau; C B Langman; U Gafter; P K Dudeja; T A Brasitus
Journal:  J Clin Invest       Date:  1986-10       Impact factor: 14.808

4.  Blood pressure development of the spontaneously hypertensive rat after concurrent manipulations of dietary Ca2+ and Na+. Relation to intestinal Ca2+ fluxes.

Authors:  D A McCarron; P A Lucas; R J Shneidman; B LaCour; T Drüeke
Journal:  J Clin Invest       Date:  1985-09       Impact factor: 14.808

5.  Calcium and sodium transport and vitamin D metabolism in the spontaneously hypertensive rat.

Authors:  H P Schedl; D L Miller; J M Pape; R L Horst; H D Wilson
Journal:  J Clin Invest       Date:  1984-04       Impact factor: 14.808

6.  Altered vitamin D metabolism in the kidney of the spontaneously hypertensive rat.

Authors:  H Kawashima
Journal:  Biochem J       Date:  1986-08-01       Impact factor: 3.857

7.  Increased plasma calcitonin levels in young spontaneously hypertensive rats: role in disturbed phosphate homeostasis.

Authors:  R J Bindels; L A van den Broek; M J Jongen; W H Hackeng; C W Löwik; C H van Os
Journal:  Pflugers Arch       Date:  1987-04       Impact factor: 3.657

8.  Abnormal vitamin D metabolism, intestinal calcium transport, and bone calcium status in the spontaneously hypertensive rat compared with its genetic control.

Authors:  P A Lucas; R C Brown; T Drüeke; B Lacour; J A Metz; D A McCarron
Journal:  J Clin Invest       Date:  1986-07       Impact factor: 14.808

  8 in total

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