Dietary Geranylgeranyl Pyrophosphate Counteracts the Benefits of Statin Therapy in Experimental Pulmonary Hypertension

BACKGROUND: The mevalonate pathway generates endogenous cholesterol and intermediates including geranylgeranyl pyrophosphate (GGPP). By reducing GGPP production, statins exert pleiotropic or cholesterol-independent effects. The potential regulation of GGPP homeostasis through dietary intake and the interaction with concomitant statin therapy is unknown.

METHODS: We developed a sensitive high-pressure liquid chromatography technique to quantify dietary GGPP and conducted proteomics, qualitative real-time polymerase chain reaction screening, and Western blot to determine signaling cascades, gene expression, protein-protein interaction, and protein membrane trafficking in wild-type and transgenic rats.

RESULTS: GGPP contents were highly variable depending on food source that differentially regulated blood GGPP levels in rats. Diets containing intermediate and high GGPP reduced or abolished the effects of statins in rats with hypoxia- and monocrotaline-induced pulmonary hypertension: this was rescuable by methyl-allylthiosulfinate and methyl-allylthiosulfinate-rich garlic extracts. In human pulmonary artery smooth muscle cells treated with statins, hypoxia activated RhoA in an extracellular GGPP-dependent manner. Hypoxia-induced ROCK2 (Rho associated coiled-coil containing protein kinase 2)/Rab10 (Ras-related protein rab-10) signaling was prevented by statin and recovered by exogenous GGPP. The hypoxia-activated RhoA/ROCK2 pathway in rat and human pulmonary artery smooth muscle cells upregulated the expression of Ca2+-sensing receptor (CaSR) and HIMF (hypoxia-induced mitogenic factor), a mechanism attenuated by statin treatment and regained with exogenous GGPP. Rab10 knockdown almost abrogated hypoxia-promoted CaSR membrane trafficking, a process diminished by statin and resumed by exogenous GGPP. Hypoxia-induced pulmonary hypertension was reduced in rats with CaSR mutated at the binding motif of HIMF and the interaction between dietary GGPP and statin efficiency was abolished. In humans fed a high GGPP diet, blood GGPP levels were increased. This abolished statin-lowering effects on plasma GGPP, and also on hypoxia-enhanced RhoA activity of blood monocytes that was rescued by garlic extracts.

CONCLUSIONS: There is important dietary regulation of GGPP levels that interferes with the effects of statin therapy in experimental pulmonary hypertension. These observations rely on a key and central role of RhoA-ROCK2 cascade activation and Rab10-faciliated CaSR membrane trafficking with subsequent overexpression and binding of HIMF to CaSR. These findings warrant clinical investigation for the treatment of pulmonary hypertension and perhaps other diseases by combining statin with garlic-derived methyl-allylthiosulfinate or garlic extracts and thus circumventing dietary GGPP variations.

Errataetall:

CommentIn: Circulation. 2021 May 4;143(18):1793-1796. - PMID 33939531

Medienart:

E-Artikel

Erscheinungsjahr:

2021

Erschienen:

2021

Enthalten in:

Zur Gesamtaufnahme - volume:143

Enthalten in:

Circulation - 143(2021), 18 vom: 04. Mai, Seite 1775-1792

Sprache:

Englisch

Beteiligte Personen:

Zhu, Liping [VerfasserIn]
Liu, Fangbo [VerfasserIn]
Hao, Qiang [VerfasserIn]
Feng, Tian [VerfasserIn]
Chen, Zeshuai [VerfasserIn]
Luo, Shengquan [VerfasserIn]
Xiao, Rui [VerfasserIn]
Sun, Mengxiang [VerfasserIn]
Zhang, Ting [VerfasserIn]
Fan, Xiaohang [VerfasserIn]
Zeng, Xianqin [VerfasserIn]
He, Jianguo [VerfasserIn]
Yuan, Ping [VerfasserIn]
Liu, Jinming [VerfasserIn]
Ruiz, Matthieu [VerfasserIn]
Dupuis, Jocelyn [VerfasserIn]
Hu, Qinghua [VerfasserIn]

Links:

Volltext

Themen:

Geranylgeranyl pyrophos-phate
Geranylgeranyl pyrophosphate
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Hydroxymethylglutaryl-CoA reductase inhibitors
Hyperten-sion, pulmonary
Journal Article
N21T0D88LX
Polyisoprenyl Phosphates
Research Support, Non-U.S. Gov't

Anmerkungen:

Date Completed 15.09.2021

Date Revised 15.09.2021

published: Print-Electronic

CommentIn: Circulation. 2021 May 4;143(18):1793-1796. - PMID 33939531

Citation Status MEDLINE

doi:

10.1161/CIRCULATIONAHA.120.046542

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM322179726