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SA JOURNAL OF DIABETES & VASCULAR DISEASE

RESEARCH ARTICLE

VOLUME 13 NUMBER 2 • DECEMBER 2016

67

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 antihyperglycaemic

effects.

Acknowledgements

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 D Abel, 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/mediacentre.

6. Rader DJ. Effect of insulin resistance, dyslipidemia and intra-abdominal 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 glandulosa

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 inhibitor 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: separation 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 dyslipidemia.

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 preconditioning

protects by activating prosurvival kinases at reperfusion.

Am J Physiol Heart

Circulat Physiol

2005;

288

: H971–H976.

23. Jonassen AK, Sack MN, Mj.s 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 phosphorylation 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, D.chaux 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 Antagonism Attenuates Obesity-

Induced Hypertension and glomerular hyperfiltration.

Hypertension

2004;

43

:

41–47.

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