Chronic cathepsin inhibition by E‐64 in Dahl salt‐sensitive rats. Issue 17 (4th September 2016)
- Record Type:
- Journal Article
- Title:
- Chronic cathepsin inhibition by E‐64 in Dahl salt‐sensitive rats. Issue 17 (4th September 2016)
- Main Title:
- Chronic cathepsin inhibition by E‐64 in Dahl salt‐sensitive rats
- Authors:
- Blass, Gregory
Levchenko, Vladislav
Ilatovskaya, Daria V.
Staruschenko, Alexander - Abstract:
- Abstract: Cysteine cathepsins are lysosomal enzymes expressed in the kidneys and other tissues, and are involved in the maturation and breakdown of cellular proteins. They have been shown to be integrally involved in the progression of many cardiovascular and renal diseases. The goal of this study was to determine the involvement of cysteine cathepsins in the development of salt‐sensitive hypertension and associated kidney damage. In our experiments, Dahl salt‐sensitive (SS) rats were fed an 8% high salt NaCl diet and intravenously infused with the irreversible cysteine cathepsin inhibitor E‐64 (1 mg/day) or the vehicle (control). Both the control and E‐64 infused groups developed significant hypertension and kidney damage, and no difference of the mean arterial pressure and the hypertension‐associated albuminuria was observed between the groups. We next tested basal calcium levels in the podocytes of both control and infused groups using confocal calcium imaging. Basal calcium did not differ between the groups, indicative of the lack of a protective or aggravating influence by the cathepsin inhibition. The efficacy of E‐64 was tested in Western blotting. Our findings corresponded to the previously reported, E‐64 induced increase in cathepsin B and L abundance. We conclude that the inhibition of cysteine cathepsins by E‐64 does not have any effects on the blood pressure development and kidney damage, at least under the studied conditions of this model of SS hypertension.Abstract: Cysteine cathepsins are lysosomal enzymes expressed in the kidneys and other tissues, and are involved in the maturation and breakdown of cellular proteins. They have been shown to be integrally involved in the progression of many cardiovascular and renal diseases. The goal of this study was to determine the involvement of cysteine cathepsins in the development of salt‐sensitive hypertension and associated kidney damage. In our experiments, Dahl salt‐sensitive (SS) rats were fed an 8% high salt NaCl diet and intravenously infused with the irreversible cysteine cathepsin inhibitor E‐64 (1 mg/day) or the vehicle (control). Both the control and E‐64 infused groups developed significant hypertension and kidney damage, and no difference of the mean arterial pressure and the hypertension‐associated albuminuria was observed between the groups. We next tested basal calcium levels in the podocytes of both control and infused groups using confocal calcium imaging. Basal calcium did not differ between the groups, indicative of the lack of a protective or aggravating influence by the cathepsin inhibition. The efficacy of E‐64 was tested in Western blotting. Our findings corresponded to the previously reported, E‐64 induced increase in cathepsin B and L abundance. We conclude that the inhibition of cysteine cathepsins by E‐64 does not have any effects on the blood pressure development and kidney damage, at least under the studied conditions of this model of SS hypertension. Abstract : Cysteine cathespins are lysosomal enzymes that regulate many cellular processes including those that are known to be important in salt‐sensitive hypertension. To determine the in vivo role of cysteine cathepsins in salt‐sensitive (SS) hypertension, the cysteine cathepsin inhibitor E‐64 was chronically infused into Dahl SS rats during a 3 week high salt diet. The development of SS hypertension and the associated renal pathology was unaffected by E‐64 treatment indicating that cysteine cathepsins may not be critically involved in SS hypertension. … (more)
- Is Part Of:
- Physiological reports. Volume 4:Issue 17(2016)
- Journal:
- Physiological reports
- Issue:
- Volume 4:Issue 17(2016)
- Issue Display:
- Volume 4, Issue 17 (2016)
- Year:
- 2016
- Volume:
- 4
- Issue:
- 17
- Issue Sort Value:
- 2016-0004-0017-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2016-09-04
- Subjects:
- Cathepsin -- cathepsin L -- cysteine proteases -- salt‐sensitive hypertension
Physiology -- Periodicals
571 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2051-817X ↗
http://physreports.physiology.org ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.14814/phy2.12950 ↗
- Languages:
- English
- ISSNs:
- 2051-817X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 1720.xml