68 CHIRAL SEPARATION OF THE INOTROPIC AND CHRONOTROPIC ACTIONS OF DIGOXIN. (1st March 2005)
- Record Type:
- Journal Article
- Title:
- 68 CHIRAL SEPARATION OF THE INOTROPIC AND CHRONOTROPIC ACTIONS OF DIGOXIN. (1st March 2005)
- Main Title:
- 68 CHIRAL SEPARATION OF THE INOTROPIC AND CHRONOTROPIC ACTIONS OF DIGOXIN
- Authors:
- Somberg, J. C.
Lin, C.
Cvetanovic, I.
Ke, X.
Molnar, J.
Ranade, V. - Abstract:
- Abstract : Background: Digoxin (D) prolongs conduction at the AV node and augments cardiac contractility by inhibition of Na+, K+-ATPase. The digoxin molecule is chiral having asymmetries at the C3 and C17 carbon centers that could give rise to stereoscopic isomers. The actions of D on cardiac conduction and contractility could be mediated through the different isoforms of Na+, K+-ATPase that exist with different isomers having different degrees of inhibition of the different isoforms. Methods: Using cyclobond chiral column we separated digoxin into two distinct chromatographic peaks each with different retention times. Optical rotation was +17° and +3° respectively for the two peaks but both isolates showed the same mass/change ratio of 780, identical to that of racemate digoxin. The effects of the isolates on cardiac contractility and AV conduction were evaluated in anesthetized guinea pigs (GP): 15 GPs were randomly given D, isolate 1 or 2. AV conduction was assessed by measuring PR interval and contractility by a Walton Brody strain gauge arch sutured to the left ventricular free wall. D or the isolates were infused continuously at 6 μg/kg/min. Results: D and isolate 1 caused a progressive increase in the PR interval while isolate 2 did not progressively increase PR. D and isolate 2 caused a progressive increase in contractility (% change from the baseline) while isolate 1 caused little change in contractility. Conclusions: We concluded that D can be chirally separatedAbstract : Background: Digoxin (D) prolongs conduction at the AV node and augments cardiac contractility by inhibition of Na+, K+-ATPase. The digoxin molecule is chiral having asymmetries at the C3 and C17 carbon centers that could give rise to stereoscopic isomers. The actions of D on cardiac conduction and contractility could be mediated through the different isoforms of Na+, K+-ATPase that exist with different isomers having different degrees of inhibition of the different isoforms. Methods: Using cyclobond chiral column we separated digoxin into two distinct chromatographic peaks each with different retention times. Optical rotation was +17° and +3° respectively for the two peaks but both isolates showed the same mass/change ratio of 780, identical to that of racemate digoxin. The effects of the isolates on cardiac contractility and AV conduction were evaluated in anesthetized guinea pigs (GP): 15 GPs were randomly given D, isolate 1 or 2. AV conduction was assessed by measuring PR interval and contractility by a Walton Brody strain gauge arch sutured to the left ventricular free wall. D or the isolates were infused continuously at 6 μg/kg/min. Results: D and isolate 1 caused a progressive increase in the PR interval while isolate 2 did not progressively increase PR. D and isolate 2 caused a progressive increase in contractility (% change from the baseline) while isolate 1 caused little change in contractility. Conclusions: We concluded that D can be chirally separated with one isolate causing progressive PR prolongation and the other contractile augmentation. (Figure ) … (more)
- Is Part Of:
- Journal of investigative medicine. Volume 53:Number 2(2005)
- Journal:
- Journal of investigative medicine
- Issue:
- Volume 53:Number 2(2005)
- Issue Display:
- Volume 53, Issue 2 (2005)
- Year:
- 2005
- Volume:
- 53
- Issue:
- 2
- Issue Sort Value:
- 2005-0053-0002-0000
- Page Start:
- S368
- Page End:
- S368
- Publication Date:
- 2005-03-01
- Subjects:
- Clinical medicine -- Periodicals
Medicine -- Research -- Periodicals
Medicine
Research -- United States
Clinical medicine
Medicine -- Research
Periodicals
616.075 - Journal URLs:
- http://journals.lww.com/jinvestigativemed/pages/default.aspx ↗
http://jim.bmj.com/ ↗
https://journals.sagepub.com/home/IMJ ↗
http://journals.lww.com ↗ - DOI:
- 10.2310/6650.2005.00206.67 ↗
- Languages:
- English
- ISSNs:
- 1081-5589
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5008.010000
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British Library STI - ELD Digital store - Ingest File:
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