Key result
Modulation of angiotensin II signaling via AT1 blockade and AT2 stimulation represents a promising therapeutic approach for inhibiting tissue fibrosis across multiple organ systems.
Why the study?
Does modulation of angiotensin II signaling prevent or ameliorate tissue fibrosis?
Does modulation of angiotensin II signaling prevent or ameliorate tissue fibrosis?
Modulation of the renin-angiotensin system, particularly via AT2 receptor activation, offers a potential therapeutic avenue for treating fibrotic diseases outside the cardiovascular system.
AT2 receptor activation may reduce fibrosis in noncardiac tissues; leaves open clinical translation pending prospective trials.
Over the last decade, it has become clear that the role of angiotensin II extends far beyond recognized renal and cardiovascular effects. The presence of an autologous renin-angiotensin system has been demonstrated in almost all tissues of the body. It is now known that angiotensin II acts both independently and in synergy with TGF-beta to induce fibrosis via the angiotensin type 1 receptor (AT1) in a multitude of tissues outside of the cardiovascular and renal systems, including pulmonary fibrosis, intra-abdominal fibrosis, and systemic sclerosis. Interestingly, recent studies have described a paradoxically regenerative effect of the angiotensin system via stimulation of the angiotensin type 2 receptor (AT2). Activation of AT2 has been shown to ameliorate fibrosis in animal models of skeletal muscle, gastrointestinal, and neurologic diseases. Clinical reports suggest a beneficial role for modulation of angiotensin II signaling in cutaneous scarring. This article reviews current knowledge on the role that angiotensin II plays in tissue fibrosis, as well as current and potential therapies targeting this system.
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Murphy et al. (2015) conducted a review in Fibrosis. Modulation of angiotensin II signaling (AT1 blockade and AT2 stimulation) was evaluated. Modulation of angiotensin II signaling via AT1 blockade and AT2 stimulation represents a promising therapeutic approach for inhibiting tissue fibrosis across multiple organ systems.
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