AN IN VITRO STUDY OF CINNAMOMUM ZEYLANICUM AS NATURAL INHIBITOR OF ANGIOTENSIN-CONVERTING ENZYME (ACE) ON SHEEP (OVIS ARIES) TISSUES

Authors

  • Ranjini H s Department of Biochemistry,Kasturba Medical College,Manipal,Manipal University,Karnataka,India
  • Padmanabha Udupa E g Department of Biochemistry,Kastuba Medical College,Manipal,Manipal University,Karnataka,India.
  • Shobha U Kamath Department of Biochemistry,Kasturba Medical College,Manipal,Manipal University,Karnataka,India.
  • Manjunath Setty Department of Pharmacognosy, MCOPS,Manipal,Manipal University,Karnataka,India.
  • Basavaraj Hadapad Department of Ayurveda,Kasturba Medical College,Manipal,Manipal University,Karnataka,India.
  • Asha Kamath Department of Community Medicine,Kasturba Medical College, Manipal,Manipal University,Karnataka,India.

DOI:

https://doi.org/10.22159/ajpcr.2016.v9i5.13424

Abstract

Objective: The present study was aimed to find the angiotensin-converting enzyme (ACE) inhibitory activity using the methanolic extract of
Cinnamomum zeylanicum (as a natural inhibitor) on sheep tissues as the enzyme source.

Methods: Hippuryl-histidyl-leucine (HHL) as a substrate, tissue ACE activity was measured spectrophotometrically at 228 nm. For an incubation
period of 30 minutes at 37°C, the linearity of ACE activity of kidney, lung, and testis enzyme was established. A known medicinal plant C. zeylanicum
was used as natural inhibitor of ACE. In this enzyme assay, inhibitory effect of methanolic extract of C. zeylanicum on kidney, lung and testicular ACE
was determined. ACE activity was confirmed by captopril, a standard inhibitor of ACE.

Results: In the presence of a methanolic extract of C. zeylanicum (10:1), ACE activity was determined and this has inhibited ACE activity very
significantly. C. zeylanicum leaves extract has reduced sheep kidney, lung, and testis ACE activity by 70.06%, 12.63%, and 20.23%, respectively.

Conclusion: Significant inhibition was observed in the kidney ACE than in lung and testis ACE activity. This can propose that there may be a possible
role in controlling blood pressure or reduction in cardiovascular diseases. Some plants with the great medicinal property may be considered as
promising sources of natural inhibitors of ACE for medicine and commercial uses. This comprehensive study may show numerous beneficial effects as
a potential therapeutic agent for lowering blood pressure.

Keywords: Angiotensin-converting enzyme, Natural angiotensin-converting enzyme inhibitor, Kinetic assay, Hippuryl-histidyl-leucine, Cinnamomum
zeylanicum, Cardiovascular diseases.

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References

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Table 1: ACE activity in tissues and percentage (%) of ACE inhibition in presence of Cinnamomum zeylanicum

Category

ACE activity in absence of inhibitor

ACE activity in presence of inhibitor

% of inhibition in presence of inhibitor

Kidney

77* (17.75,17.79)

32* (3.55,5.93)

06

Lung

69* (21.66,21.74)

95* (12.66,20.63)

63

Testis

50* (28.90,29.61)

53* (16.69,26.1)

23

*ACE activity is expressed as μm of hippuric acid released/g/minute, *data is expressed in median (IQR), *number of trials carried is in triplicates (n=3). *p<0.05, ACE: Angiotensin converting enzyme, IQR: Interquartile range, C. zeylanicum: Cinnamomum zeylanicum

Table 2: ACE activity and percentage (%) of ACE inhibition in presence of captopril

Category

ACE activity in presence of captopril

% of inhibition in presence of captopril

Kidney

48* (1.23,1.66)

67

Lung

06* (6.71,9.84)

84

Testis

37* (9.15,16.08)

28

*ACE activity is expressed as μm of hippuric acid released/g/minute, *data were expressed in median (IQR), *number of trials carried is in triplicates (n=3), *p<0.05, ACE: Angiotensin converting enzyme, IQR: Interquartile range

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Published

01-09-2016

How to Cite

H s, R., P. U. E g, S. U. Kamath, M. Setty, B. Hadapad, and A. Kamath. “AN IN VITRO STUDY OF CINNAMOMUM ZEYLANICUM AS NATURAL INHIBITOR OF ANGIOTENSIN-CONVERTING ENZYME (ACE) ON SHEEP (OVIS ARIES) TISSUES”. Asian Journal of Pharmaceutical and Clinical Research, vol. 9, no. 5, Sept. 2016, pp. 249-52, doi:10.22159/ajpcr.2016.v9i5.13424.

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