» Articles » PMID: 27713282

Combating Combination of Hypertension and Diabetes in Different Rat Models

Overview
Publisher MDPI
Specialty Chemistry
Date 2016 Oct 8
PMID 27713282
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Rat experimental models are used extensively for studying physiological mechanisms and treatments of hypertension and diabetes co-existence. Each one of these conditions is a major risk factor for cardiovascular disease (CVD), and the combination of the two conditions is a potent enhancer of CVD. Five major animal models that advanced our understanding of the mechanisms and therapeutic approaches in humans are discussed in this review: Zucker, Goto-Kakizaki, SHROB, SHR/NDmcr-cp and Cohen Rosenthal diabetic hypertensive (CRDH) rats. The use of various drugs, such as angiotensin-converting enzyme (ACE) inhibitors (ACEIs), various angiotensin receptor blockers (ARBs), and calcium channel blockers (CCBs), to combat the effects of concomitant pathologies on the combination of diabetes and hypertension, as well as the non-pharmacological approach are reviewed in detail for each rat model. Results from experiments on these models indicate that classical factors contributing to the pathology of hypertension and diabetes combination-Including hypertension, hyperglycemia, hyperinsulinemia and hyperlipidemia-can now be treated, although these treatments do not completely prevent renal complications. Animal studies have focused on several mechanisms involved in hypertension/diabetes that remain to be translated into clinical medicine, including hypoxia, oxidative stress, and advanced glycation. Several target molecules have been identified that need to be incorporated into a treatment modality. The challenge continues to be the identification and interpretation of the clinical evidence from the animal models and their application to human treatment.

Citing Articles

Transient receptor potential cation channel 6 contributes to kidney injury induced by diabetes and hypertension.

Wang Z, Fu Y, do Carmo J, da Silva A, Li X, Mouton A Am J Physiol Renal Physiol. 2021; 322(1):F76-F88.

PMID: 34866402 PMC: 8742740. DOI: 10.1152/ajprenal.00296.2021.


Type 2 diabetes mellitus in the Goto-Kakizaki rat impairs microvascular function and contributes to premature skeletal muscle fatigue.

Frisbee J, Lewis M, Kasper J, Chantler P, Wiseman R J Appl Physiol (1985). 2018; 126(3):626-637.

PMID: 30571284 PMC: 6459383. DOI: 10.1152/japplphysiol.00751.2018.


Chronic atorvastatin and exercise can partially reverse established skeletal muscle microvasculopathy in metabolic syndrome.

Lemaster K, Frisbee S, Dubois L, Tzemos N, Wu F, Lewis M Am J Physiol Heart Circ Physiol. 2018; 315(4):H855-H870.

PMID: 29932769 PMC: 6230898. DOI: 10.1152/ajpheart.00193.2018.


Honey: a novel antioxidant.

Erejuwa O, Sulaiman S, Ab Wahab M Molecules. 2012; 17(4):4400-23.

PMID: 22499188 PMC: 6268297. DOI: 10.3390/molecules17044400.

References
1.
Sampanis C, Zamboulis C . Arterial hypertension in diabetes mellitus: from theory to clinical practice. Hippokratia. 2008; 12(2):74-80. PMC: 2464302. View

2.
Huang B, Wu P, Popov K, Harris R . Starvation and diabetes reduce the amount of pyruvate dehydrogenase phosphatase in rat heart and kidney. Diabetes. 2003; 52(6):1371-6. PMC: 2147665. DOI: 10.2337/diabetes.52.6.1371. View

3.
Izuhara Y, Nangaku M, Takizawa S, Takahashi S, Shao J, Oishi H . A novel class of advanced glycation inhibitors ameliorates renal and cardiovascular damage in experimental rat models. Nephrol Dial Transplant. 2007; 23(2):497-509. DOI: 10.1093/ndt/gfm601. View

4.
Miyata T, Dan T . Inhibition of advanced glycation end products (AGEs): an implicit goal in clinical medicine for the treatment of diabetic nephropathy?. Diabetes Res Clin Pract. 2008; 82 Suppl 1:S25-9. DOI: 10.1016/j.diabres.2008.09.012. View

5.
Janssen U, Vassiliadou A, Riley S, Phillips A, Floege J . The quest for a model of type II diabetes with nephropathy: the Goto Kakizaki rat. J Nephrol. 2004; 17(6):769-73. View