Background Image
Table of Contents Table of Contents
Previous Page  18 / 67 Next Page
Information
Show Menu
Previous Page 18 / 67 Next Page
Page Background

CARDIOVASCULAR JOURNAL OF AFRICA • Vol 24, No 2, March 2013

16

AFRICA

The treatment with

P

glandulosa

was able to alleviate

this, thereby adding to the myocardial protection observed.

To highlight this argument, in the present study both the ACE

inhibitor and

P

glandulosa

treatment significantly improved

urinary flow of the animals, in conjunction with lowering the

blood pressure. Although this was not measured in the current

study, we speculate that vasopressin production and aldosterone

levels were elevated in the HFD rats.

P glandulosa

treatment may

affect the levels of either of these hormones, or it may provide

a different, hitherto unrecognised mechanism of lowering blood

pressure in the animals.

Conclusion

The present study has confirmed our previous results that

the dried and ground pods of the

P

glandulosa

tree have

anti-hyperglycaemic effects. In addition we have conclusively

shown that this treatment was cardioprotective, as determined

by the infarct-sparing effects, and anti-hypertensive without

affecting the body weight or the intra-peritoneal fat depots of the

animals. The results indicated that key proteins involved in the

cardioprotective PI-3-kinase/PKB/Akt pathway were affected in

a manner that may be causal to this protection.

With regard to the anti-hypertensive effects, the results

indicated water retention, possibly coupled with vasoconstriction

in the HFD animals, while ingestion of

P

glandulosa

alleviated

both water retention and hypertension. Treatment of pre-diabetes,

type 2 diabetes or hypertension with

P

glandulosa

therefore

poses potentially beneficial health effects besides its anti-

hyperglycaemic effects.

We declare a contractual agreement between the University of Stellenbosch

and Dormell Properties 528 (Pty) Ltd (registration number: 2005/031723/07),

the company licensing Conbrio Brands (Pty) Ltd to distribute the dried and

ground pods of

Prosopis glandulosa

. We further declare that there was no

personal financial gain for the researchers involved in this work.

We acknowledge grant money from Dormell Properties to partially fund

the work as well as a THRIP grant from the NRF to complement this. In

addition, we acknowledge the kind gift of the CIRKO mice from Prof DAbel,

University of Utah, Salt Lake City, USA.

References

1.

Felger RS. Mesquite in Indian cultures of the Southwestern North

America. In Simpson BB (ed).

Mesquite:

Its

Biology

in

Two

Desert

Scrub

Ecosystems

. Stroudsburg, PA: Dowden, Hutchinson & Ross,

1977: 150–176.

2.

Harden ML, Zolfaghari R. Nutritive composition of green and ripe

pods of honey mesquite (

Prosopis

glandulosa

, Fabaceae).

Econom Bot

1988;

42

: 522–532.

3.

National Cholesterol Education Program (NCEP) Expert Panel on

Detection, Evaluation and Treatment of High Blood Cholesterol in

Adults. Third report of the NCEP – Adult Treatment panel III, final

report.

Circulation

2002;

106

: 3143–3421.

4.

Balkau B, Charles MA. Comment on the provisional report from

the WHO Consultation. European Group for the Study of Insulin

Resistance (EGIR).

Diabetes Med

1999:

16

: 442–443.

5.

Factsheet of the World Health Organisation 2011;

www.who.int/media

-

centre.

6.

Rader DJ. Effect of insulin resistance, dyslipidemia and intra-abdomi-

nal adiposity on the development of cardiovascular disease and diabetes

mellitus

. Am

J Med

2007;

120

: S12–S18.

7.

Malviya N, Jain S, Malviya S. Antidiabetic potential of medicinal

plants.

Acta Poloniae Pharmaceut

– Drug Res

2010;

67

: 113–118.

8.

George C, Huisamen B, Lochner A. The efficacy of

Prosopis

glan-

dulosa

as antidiabetic treatment in rat models of diabetes and insulin

resistance.

J Ethnopharm

2011;

137

: 298–304.

9.

Samoylenko V, Ashfaq MK, Jacob M,

et

al

. Indolizidine, anti-infective

and antiparasitic compounds from

Prosopis glandulosa

var.

glandulosa

.

J Natl Prod

2009;

72

: 92–98.

10. Huisamen B, Genis A, Lochner A. Pre-treatment with a DPP-4 inhibi-

tor is infarct sparing in hearts from obese, pre-diabetic rats.

Cardiovasc

Drugs Ther

2011;

25

: 13–20.

11. Naderali EK, Pickavance LC, Wilding JPH, Williams G. Diet-induced

endothelial dysfunction in the rat is independent of the degree of

increase in total body weight.

Clin

Sci

2001;

100

: 635–641.

12. Srinivastan K, Biswanad B, Asrat L, Kaul CL, Ramarao P. Combination

of high-fat diet-fed and low-dose streptozotocin-treated rat: A model

for type 2 diabetes and pharmacological screening.

Pharm

Res

2005;

52

: 313–320.

13. Pickavance LC, Tadayyon M, Widdowson PS, Buckinham RE, Wilding

JPH. Therapeutic index for rosiglitazone in dietary obese rats: separa-

tion of efficacy and haemodilution.

Br

J Pharm

1999;

128

: 1570–1576.

14. Belke DD, Betuing S, Tuttle MJ,

et

al.

Insulin signaling coordinately

regulates cardiac size, metabolism, and contractile protein isoform

expression

.

J Clin

Invest

2002;

109

: 629–639.

15. Lochner A, Genade S, Moolman JA. Ischemic preconditioning: infarct

size is a more reliable endpoint than functional recovery.

Basic

Res

Cardiol

2003;

98

: 337–346.

16. Bradford MM, A rapid and sensitive method for the quantitation of

microgram quantities of protein utilizing the principle of protein-dye

binding.

Ann Biochem

1976;

72

: 248–254.

17. Ross AH, Gericke A. Phosphorylation keeps PTEN phosphatase closed

for business.

Proc Nat Acad

Sci

2009;

106

: 1297–1298.

18. Oudit GY, Penninger JM. Cardiac regulation by phosphoinositide

3-kinases and PTEN.

Cardiovasc Res

2009;

82

: 250–260.

19. Kurukulasuriya LR, Stas S, Lastra G, Manrique C, Sowers JR.

Hypertension in obesity.

Med Clin North Am

2011;

95

: 903–917.

20. Franssen R, Monajemi H, Stroes ES, Kastelein JJ. Obesity and dyslipi-

demia.

Med Clin North Am

2011;

95

: 893–902.

21. Mentreddy SRS, Mohamed AI, Rimando AM. Medicinal plants with

hypoglycemic/anti-hyperglycemic properties: A review.

Proc Assoc Adv

Indust Crops Conf

2005;

20

; 341–353.

22. Hausenloy DJ, Tsang A, Mocanu MM, Yellon DM. Ischemic precondi-

tioning protects by activating prosurvival kinases at reperfusion.

Am

J

Physiol Heart Circulat Physiol

2005;

288

: H971–H976.

23. Jonassen AK, Sack MN, Mjøs OD, Yellon DM. Myocardial protection

by insulin at reperfusion requires early administration and is mediated

via Akt and p70s6 kinase cell-survival signaling.

Circ

Res

2001;

89

:

1191–1198.

24. Di R, Wu X, Chang Z, Zhao X,

et

al.

S6K inhibition renders cardiac

protection against myocardial infarction through PDK1 phosphoryla-

tion of Akt.

Biochem

J

2012;

441

: 199–207

25. Huisamen B, Donthi, Lochner A. Insulin in combination with vanadate

stimulates glucose transport in isolated cardiomyocytes from obese

Zucker rats.

Cardiovasc Drugs Ther

2001;

15:

445–452.

26. Ahloulay M, Schmitt F, Déchaux M, Bankir L. Vasopressin and urinary

concentrating activity in diabetes mellitus.

Diabetes Metab

1999;

25

:

213–22.

27. De Paula RB, Da Silva AA, Hall E. Aldosterone AntagonismAttenuates

Obesity-Induced Hypertension and glomerular hyperfiltration.

Hypertension

2004;

43

: 41–47.

28. Hall JE, Brands MW, Dixon WN, Smith Jr NJ. Obesity-induced hyper-

tension, Renal function and systemic hemodynamics.

Hypertension

1993;

22

: 292–299.

29. Lee HB, Blaufox MD. Blood volume in the Rat.

J Nucl Med

1985;

25:

72–76.