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    Review of 'Understanding (apo-) soluble guanylate cyclase allosterism and its therapeutic implications'

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    Understanding (apo-) soluble guanylate cyclase allosterism and its therapeutic implicationsCrossref
    A highly imporatnt contribution to sGC pharmacology, with direct clinical implications.
    Average rating:
        Rated 5 of 5.
    Level of importance:
        Rated 5 of 5.
    Level of validity:
        Rated 5 of 5.
    Level of completeness:
        Rated 5 of 5.
    Level of comprehensibility:
        Rated 5 of 5.
    Competing interests:
    I am a co-inventor on WO/2021/239623 / US 11,480,583 and WO/2023/204698. I am a consortium member of REPO-TRIAL which conduts the REPO-STROKE and REPO-HFpFF clinical trials.

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    Understanding (apo-) soluble guanylate cyclase allosterism and its therapeutic implications

    Nitric oxide (NO) is a widely distributed gasotransmitter binding to the heme of soluble guanylate cyclase (sGC) to stimulate the formation of the second messenger cyclic GMP. In disease, two pathomechanisms can occur, scavenging of NO by reactive oxygen species so that sGC is insufficiently stimulated, and oxidative damage of sGC resulting in heme loss and a NO-insensitive apo-form of sGC. To address this therapeutically, two pharmacological principles have entered the clinic or clinical development. sGC stimulators (sGCs) allosterically sensitize sGC for lower NO levels to reach physiological cGMP levels again; sGC activators (sGCa) bind to the empty heme pocket of apo-sGC to recover cGMP formation. Here we show in vitro and in vivo that this dichotomic pharmacology of sGCs/sGC and sGCa/apo-sGC is wrong. Instead apo-sGC is both activated by sGCa and allosterically modulated by sGC stimulators. The sGCs binding site in sGC and apo-sGC, however, is redox sensitive explaining why it has been previously missed in apo-sGC preparations generated for example by using heme oxidants such as 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ). Moreover, sGCs synergised with sGCa on apo-sGC in a supra-additive manner similar to the synergy between NO and sGCs on sGC. Our findings provide functional evidence including ischemic stroke, where apo-sGC rather than sGC is detectable, for identical modulation of sGC and apo-sGC by sGCs. This necessitates a revision of the dichotomic sGC/apo-sGC pharmacology and expands the therapeutic potential of sGCs and sGCa both individually and in combination.
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      Review information

      10.14293/S2199-1006.1.SOR-MED.A7RXGP.v1.RTHCUJ
      This work has been published open access under Creative Commons Attribution License CC BY 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Conditions, terms of use and publishing policy can be found at www.scienceopen.com.

      Pharmacology & Pharmaceutical medicine
      stroke,cyclic GMP,soluble guanylate cyclase stimulators,apo-soluble guanylate cyclase,apo-soluble guanylate cyclase activators

      Review text

      In the Introduction, the chemical name of ODQ misses the square brackets. Correct representation is 1H-[1,2,4]oxadiazolo[4,3a]quinoxalin-1-one.

      Under Competing Interests, update the final sentence: "H.H.H.W.S and A.P. are inventors of WO/2023/204698 titled "Diagnosis and/or treatment of heart failure with preserved ejection fraction."

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