Literature DB >> 10327105

Washout of I-123 meta-iodobenzylguanidine for assessing cardiac sympathetic activity with progression of hypertension in Dahl salt-sensitive rats.

H Takatsu1, T Noda, M Arai, A Kunishima, M Inoue, S Tazawa, H Kurosawa, K Nishigaki, H Fujiwara.   

Abstract

BACKGROUND: To evaluate cardiac sympathetic activity, a simple method should be developed to replace such complex methods as the spillover rate of tritiated norepinephrine (3H-norepinephrine) or microneurography of sympathetic nerve activity. The goal of this study is to evaluate cardiac sympathetic activities by analyzing the washout of I-123 meta-iodobenzylguanidine (123I-MIBG), a radiolabeled norepinephrine analogue, in Dahl salt-sensitive (DS) rats as it relates to the progression of hypertension. METHODS AND
RESULTS: Dahl salt-resistant (DR) rats and DS rats were fed an 8 % salt diet starting at age 5 weeks. Marked hypertension and cardiac hypertrophy developed in the DS rats, whereas DR rats remained normotensive. Then the time-activity curves of 123I-MIBG from 15 to 200 minutes were obtained from both DS and DR strains at ages 8, 11, and 13 weeks using dynamic scintigraphic analysis. We also examined the nonneuronal washout of 123I-MIBG using dynamic scintigraphic studies in desipramine pretreated normal rats. In the preliminary study with desipramine pretreatment, the majority of the nonneuronal 123I-MIBG washout occurred by 90 minutes after injection. Therefore the late-phase washout in the control rats was found to reflect the neuronal washout. We then applied exponential curve fitting to the time activity curves acquired in the 90- to 200-minute period after 123I-MIBG injection in both DR and DS rats. When we compared the coefficients of these washout curves in the DS and DR rats as an index of cardiac sympathetic activities, the coefficient values remained high during all stages in DS rats, whereas they decreased with age in DR rats.
CONCLUSION: Measurement of late-phase 123I-MIBG washout may be a useful tool for assessing the change in sympathetic activity in the progression of hypertension without the influence of extraneuronal washout of 123I-MIBG and left ventricular hypertrophy.

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Year:  1999        PMID: 10327105     DOI: 10.1016/s1071-3581(99)90081-8

Source DB:  PubMed          Journal:  J Nucl Cardiol        ISSN: 1071-3581            Impact factor:   5.952


  32 in total

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Journal:  Cardiologia       Date:  1957

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Authors:  S Julius
Journal:  Am J Cardiol       Date:  1991-04-22       Impact factor: 2.778

3.  Influence of specific activity on myocardial uptake of 123I-mIBG in rats.

Authors:  B H Mock; M M Tuli
Journal:  Nucl Med Commun       Date:  1988-09       Impact factor: 1.690

4.  Abnormal I-123 metaiodobenzylguanidine myocardial washout and distribution may reflect myocardial adrenergic derangement in patients with congestive cardiomyopathy.

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Journal:  Circulation       Date:  1988-11       Impact factor: 29.690

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Journal:  Circulation       Date:  1981-10       Impact factor: 29.690

6.  Modulation of left ventricular iodine-125-MIBG accumulation in cardiomyopathic Syrian hamsters using the renin-angiotensin system.

Authors:  H Takatsu; Y Uno; H Fujiwara
Journal:  J Nucl Med       Date:  1995-06       Impact factor: 10.057

7.  Transition from compensatory hypertrophy to dilated, failing left ventricles in Dahl salt-sensitive rats.

Authors:  M Inoko; Y Kihara; I Morii; H Fujiwara; S Sasayama
Journal:  Am J Physiol       Date:  1994-12

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Authors:  M Esler; G Jennings; G Lambert
Journal:  Am J Hypertens       Date:  1989-03       Impact factor: 2.689

9.  Failure of salt loading to inhibit tissue norepinephrine turnover in prehypertensive Dahl salt-sensitive rats.

Authors:  C P Genain; S R Reddy; C E Ott; G R Van Loon; T A Kotchen
Journal:  Hypertension       Date:  1988-12       Impact factor: 10.190

10.  Comparison of the sodium dependency of uptake of meta-lodobenzylguanidine and norepinephrine into cultured bovine adrenomedullary cells.

Authors:  S Jaques; M C Tobes; J C Sisson; J A Baker; D M Wieland
Journal:  Mol Pharmacol       Date:  1984-11       Impact factor: 4.436

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