Previous Page  10 / 12 Next Page
Information
Show Menu
Previous Page 10 / 12 Next Page
Page Background

Page 62

Notes:

Volume 3

Journal of Nursing Research and Practice

Nursing and Heart 2019

April 22-23, 2019

Nursing Education and Evidence Based Practice Conference

Heart Conference

April 22-23, 2019 Dubai, UAE

World

4

th

International

&

Neural regulation of cardiovascular function during inhibition of nitric oxide synthesis in rats

Meenakshi Chaswal, Shobha Das, Jagdish Prasad, Anju Katyal

and

Mohammad Fahim

Vardhman Mahavir Medical College, India

D

eficient synthesis of Nitric Oxide (NO) is an important component not only of hypertension but also of cardiac autonomic

dysfunction. It is not known whether the hemodynamic and cardiac autonomic derangements associated with NO deficiency are

due to interference of direct vasodilatory action of NO or involve some neuro-humoral system. In order to clarify and fill in the existing

gaps, we assessed cardiac autonomic functions during acute and chronic inhibition of NO synthesis by NG-nitro-L-arginine methyl

ester (L-NAME) in adult Wistar rats. Baroreflex Sensitivity (BRS) and Heart Rate Variability (HRV) were measured for assessment of

cardiac autonomic functions. We further evaluated the contribution of oxidative stress, sympathetic nervous system as well as renin-

angiotensin system, to the changes in neural regulation of cardiovascular system during NO inhibition. Serum Malondialdehyde

(MDA) was measured as a marker of oxidative stress. “Subtractive approach” of chemical sympathectomy by 6-hydroxydopamine

was used to study the role of sympathetic nervous system and extent of involvement of renin-angiotensin system was studied using

angiotensin II type I receptor blocker, losartan. Our results reveal that sympathectomy completely reversed not only pressure rise but

also cardiac autonomic dysfunction in chronic L-NAME treated rats whereas a partial reversal that too of only cardiac autonomic

responses was observed in acute L-NAME treated rats. These results thus suggest that, it is the inhibition of direct vasorelaxant action

of NO which mediates the effects seen after acute L-NAME administration on the other hand, effects of long-term inhibition of NO

synthesis are primarily mediated through sympathoexcitation. Thus, the role of sympathetic nervous system in L-NAME model

is time dependent and its contribution becomes important with longer NO inhibition. In addition, administration of losartan had

no effect on pressor response of L-NAME irrespective of its duration, but it was effective in restoration of autonomic derangement

especially after chronic L-NAME treatment.

balachandranmeenakshi@ymail.com

J Nursing Research and Practice, Volume 3

DOI: 10.4172/2632-251X-C3-009