9 Importance of intrinsic cardiac nerves in both direct and remote ischaemic conditioning. (17th November 2015)
- Record Type:
- Journal Article
- Title:
- 9 Importance of intrinsic cardiac nerves in both direct and remote ischaemic conditioning. (17th November 2015)
- Main Title:
- 9 Importance of intrinsic cardiac nerves in both direct and remote ischaemic conditioning
- Authors:
- Pickard, JMJ
Davidson, SM
Yellon, DM - Abstract:
- Abstract : Rationale: The intrinsic cardiac nervous system is important in our understanding of cardiac physiology. Using a pharmacological approach, we investigated the hypotheses that these nerves play a role in (1) direct ischaemic preconditioning (IPC) and (2) the cardioprotection offered by the humoral mediator of remote ischaemic conditioning (RIC). Methods: For the IPC experiment, isolated Langendorff perfused rat hearts were subjected to one of the following conditions; (1) Control + Hexamethonium (50 µM), (2) IPC (3 × 5-min global ischaemia) + Hexamethonium, (3) IPC alone. All hearts were subjected to 35-min ischaemia followed by 60-min reperfusion. In the second study, RIC (4 × 5 min hindlimb ischaemia/reperfusion) or sham was performed on anaesthetised rats, before exsanguination and centrifugation to obtain platelet-free plasma. After dialysis across a <12–14 kDa membrane, the dialysate was perfused through a naïve isolated Langendorff rat heart prior to an ischaemia-reperfusion injury, as described above. The hearts were assigned to the following groups; (1) Sham dialysate, (2) RIC dialysate, (3) Sham+hexamethonium (50 µM), (4) RIC+hexamethonium, (5) Sham+atropine (100 nM), (6) RIC+atropine (100 nM). All hearts were analysed for infarct size using triphenyl-tetrazolium chloride staining. Data presented as mean ± SEM and analysed using analysis of variance. Results: Hexamethonium partially, but significantly, abrogated IPC-mediated cardioprotection (Control =Abstract : Rationale: The intrinsic cardiac nervous system is important in our understanding of cardiac physiology. Using a pharmacological approach, we investigated the hypotheses that these nerves play a role in (1) direct ischaemic preconditioning (IPC) and (2) the cardioprotection offered by the humoral mediator of remote ischaemic conditioning (RIC). Methods: For the IPC experiment, isolated Langendorff perfused rat hearts were subjected to one of the following conditions; (1) Control + Hexamethonium (50 µM), (2) IPC (3 × 5-min global ischaemia) + Hexamethonium, (3) IPC alone. All hearts were subjected to 35-min ischaemia followed by 60-min reperfusion. In the second study, RIC (4 × 5 min hindlimb ischaemia/reperfusion) or sham was performed on anaesthetised rats, before exsanguination and centrifugation to obtain platelet-free plasma. After dialysis across a <12–14 kDa membrane, the dialysate was perfused through a naïve isolated Langendorff rat heart prior to an ischaemia-reperfusion injury, as described above. The hearts were assigned to the following groups; (1) Sham dialysate, (2) RIC dialysate, (3) Sham+hexamethonium (50 µM), (4) RIC+hexamethonium, (5) Sham+atropine (100 nM), (6) RIC+atropine (100 nM). All hearts were analysed for infarct size using triphenyl-tetrazolium chloride staining. Data presented as mean ± SEM and analysed using analysis of variance. Results: Hexamethonium partially, but significantly, abrogated IPC-mediated cardioprotection (Control = 44.4 ± 4.0%, IPC+Hex = 31.8 ± 5.0%, p < 0.05 vs IPC = 14.2 ± 1.9%). RIC dialysate significantly protected a naïve heart from injury (RIC = 27.6 ± 2.3 vs Control = 42.9 ± 1.2, p < 0.05). Both hexamethonium (45.8 ± 2.5%) and atropine (36.5 ± 3.4%) abrogated dialysate-mediated protection. Conclusion: Intrinsic cardiac nerves seem to be important in the induction of protection both in IPC and the response to the humoral RIC mediator. … (more)
- Is Part Of:
- Heart. Volume 101(2015)Supplement 6
- Journal:
- Heart
- Issue:
- Volume 101(2015)Supplement 6
- Issue Display:
- Volume 101, Issue 6 (2015)
- Year:
- 2015
- Volume:
- 101
- Issue:
- 6
- Issue Sort Value:
- 2015-0101-0006-0000
- Page Start:
- A3
- Page End:
- A3
- Publication Date:
- 2015-11-17
- Subjects:
- Heart -- Diseases -- Treatment -- Periodicals
Cardiology -- Periodicals
616.12 - Journal URLs:
- http://www.bmj.com/archive ↗
http://heart.bmj.com ↗
http://www.heartjnl.com ↗ - DOI:
- 10.1136/heartjnl-2015-308734.9 ↗
- Languages:
- English
- ISSNs:
- 1355-6037
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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