Key result
AT2 receptor stimulation with compound 21 promoted tissue protection in experimental disease models without exerting an antihypertensive effect.
Why the study?
Do AT2 receptor agonists promote tissue protection in experimental disease models?
Do AT2 receptor agonists promote tissue protection in experimental disease models?
AT2 receptor agonists demonstrate tissue-protective, anti-inflammatory, and anti-apoptotic effects in preclinical models, highlighting their potential as a novel therapeutic class.
AT2 agonists may confer tissue protection independent of blood pressure; leaves open clinical translation from experimental models.
PURPOSE OF REVIEW: Research about the angiotensin AT2 receptor (AT2R) has been hampered in the past by the lack of a specific and selective agonist with in-vivo stability. Such an eagerly awaited agonist, compound 21, has recently become available, giving momentum to AT2R research which so far has resulted in 14 original publications. This article is intending to review those publications which address AT2R function by direct in-vivo stimulation instead of indirect approaches such as receptor blockade or genetic alteration of AT2R expression. RECENT FINDINGS: Studies reviewed in this article looked at the effect of AT2R stimulation in disease models of hypertension, renal disease, stroke, Alzheimer's disease and myocardial infarction. AT2R stimulation does not have an antihypertensive effect, but promoted tissue protection in all models in which it was tested. Antiinflammation and antiapoptosis seem important features of the AT2R underlying improved outcome in experimental disease models. SUMMARY: Availability of nonpeptidic, orally active AT2R agonists will facilitate future AT2R research and hopefully contribute to the clarification of many still open questions regarding AT2R signalling and function. Furthermore, AT2R agonists represent a potential novel class of drugs and are expected to enter a phase I clinical study in 2012.
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Steckelings et al. (2012) conducted a review in Hypertension, renal disease, stroke, Alzheimer's disease, and myocardial infarction. AT2 receptor agonists (compound 21) was evaluated. AT2 receptor stimulation with compound 21 promoted tissue protection in experimental disease models without exerting an antihypertensive effect.
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