General Information:
Id: | 11,680 (click here to show other Interactions for entry) |
Diseases: |
Metabolic
Muscular |
Mus musculus | |
ACE2 KO mouse | |
undifferentiated mouse C2C12 myoblast cells | |
article/cited | |
Reference: | Cao X et al.(2019) Angiotensin-converting enzyme 2 regulates endoplasmic reticulum stress and mitochondrial function to preserve skeletal muscle lipid metabolism Lipids Health Dis 18: 207 [PMID: 31775868] |
Interaction Information:
Comment | Activation of ACE2 can ameliorate ER stress and mitochondrial function, which slightly accompanied by reduced TG content and down-regulated the expression of skeletal muscle lipogenic proteins in the db/db mice. |
Formal Description Interaction-ID: 116080 |
gene/protein decreases_activity of |
Drugbank entries | Show/Hide entries for ACE2 |
Comment | ACE2 improves skeletal muscle lipid metabolism in vitro and in vivo. |
Formal Description Interaction-ID: 116081 |
gene/protein increases_activity of process |
Drugbank entries | Show/Hide entries for ACE2 |
Comment | Endogenous ACE2 improved lipid metabolism through the IKKbeta/NFkappaB/IRS-1 pathway in skeletal muscle. |
Formal Description Interaction-ID: 116082 |
gene/protein increases_activity of process IKBKB/NFKB1/IRS1 signaling |
Drugbank entries | Show/Hide entries for ACE2 |
Comment | Activation of ACE2 can ameliorate ER stress and mitochondrial function, which slightly accompanied by reduced TG content and down-regulated the expression of skeletal muscle lipogenic proteins in the db/db mice. |
Formal Description Interaction-ID: 116085 |
gene/protein increases_activity of cellular component |
Drugbank entries | Show/Hide entries for ACE2 |
Comment | Activation of ACE2 can ameliorate ER stress and mitochondrial function, which slightly accompanied by reduced triglyceride (TG) content and down-regulated the expression of skeletal muscle lipogenic proteins in the db/db mice. |
Formal Description Interaction-ID: 116086 |
gene/protein decreases_quantity of drug/chemical compound |
Drugbank entries | Show/Hide entries for ACE2 |
Comment | Activation of ACE2 can ameliorate ER stress and mitochondrial function, which slightly accompanied by reduced triglyceride (TG) content and down-regulated the expression of skeletal muscle lipogenic proteins in the db/db mice. |
Formal Description Interaction-ID: 116087 |
gene/protein decreases_expression of gene/protein lipogenic proteins |
Drugbank entries | Show/Hide entries for ACE2 |
Comment | The ACE2 mRNA levels were indeed reduced in the skeletal muscle of the ACE2 KO mice. They exhibited breakage of fibers and disorder of morphology. The skeletal muscle TG content was significantly higher in ACE2 KO mice than in WT mice. |
Formal Description Interaction-ID: 116098 |
organism model ACE2 KO mouse decreases_expression of gene/protein |
Drugbank entries | Show/Hide entries for ACE2 |
Comment | ACE2 was overexpressed in the C2C12 cells to evaluate its role in lipid metabolism and ER stress by RT-PCR analysis in vitro. Firstly, ACE2 has been proved to be indeed overexpressed after the adenoviruses infect. Secondly, the mRNA levels of fatty acid oxidation-related genes, PPARalpha, PPARgamma, and CPT1A were increased, and little change was observed in PGC-1alpha and MCAD in ACE2-overexpressing C2C12 cells. The results showed that the overexpression of ACE2 significantly improved fatty acid oxidation and ER stress. |
Formal Description Interaction-ID: 116107 |
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Drugbank entries | Show/Hide entries for ACE2 or PPARA |
Comment | ACE2 was overexpressed in the C2C12 cells to evaluate its role in lipid metabolism and ER stress by RT-PCR analysis in vitro. Firstly, ACE2 has been proved to be indeed overexpressed after the adenoviruses infect. Secondly, the mRNA levels of fatty acid oxidation-related genes, PPARalpha, PPARgamma, and CPT1A were increased, and little change was observed in PGC-1alpha and MCAD in ACE2-overexpressing C2C12 cells. The results showed that the overexpression of ACE2 significantly improved fatty acid oxidation and ER stress. |
Formal Description Interaction-ID: 116108 |
|
Drugbank entries | Show/Hide entries for ACE2 or PPARG |
Comment | ACE2 was overexpressed in the C2C12 cells to evaluate its role in lipid metabolism and ER stress by RT-PCR analysis in vitro. Firstly, ACE2 has been proved to be indeed overexpressed after the adenoviruses infect. Secondly, the mRNA levels of fatty acid oxidation-related genes, PPARalpha, PPARgamma, and CPT1A were increased, and little change was observed in PGC-1alpha and MCAD in ACE2-overexpressing C2C12 cells. The results showed that the overexpression of ACE2 significantly improved fatty acid oxidation and ER stress. |
Formal Description Interaction-ID: 116109 |
|
Drugbank entries | Show/Hide entries for ACE2 or CPT1A |
Comment | The results showed that the overexpression of ACE2 in the C2C12 cells significantly improved fatty acid oxidation and ER stress. |
Formal Description Interaction-ID: 116110 |
gene/protein increases_activity of process |
Drugbank entries | Show/Hide entries for ACE2 |
Comment | ACE2 was first reported to play a notable role on intramuscular fat regulation by improving endoplasmic reticulum and mitochondrial function. |
Formal Description Interaction-ID: 116113 |
gene/protein increases_activity of cellular component |
Drugbank entries | Show/Hide entries for ACE2 |
Comment | The results showed that the overexpression of ACE2 in the C2C12 cells significantly improved fatty acid oxidation and ER stress. |
Formal Description Interaction-ID: 116114 |
gene/protein decreases_activity of |
Drugbank entries | Show/Hide entries for ACE2 |
Comment | ACE2 was first reported to play a notable role on intramuscular fat regulation by improving endoplasmic reticulum and mitochondrial function. |
Formal Description Interaction-ID: 116115 |
gene/protein increases_activity of cellular component |
Drugbank entries | Show/Hide entries for ACE2 |
Comment | The protein levels of lipogenesis proteins ACCalpha and SREBP-1C increased in the ACE2 KO mice, and decreased in the ACE2-overexpressing db/db mice. These results suggested that ACE2 may regulate intramuscular fat accumulate in mice. |
Formal Description Interaction-ID: 116142 |
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Drugbank entries | Show/Hide entries for ACE2 or ACACA |
Comment | The protein levels of lipogenesis proteins ACCalpha and SREBP-1C increased in the ACE2 KO mice, and decreased in the ACE2-overexpressing db/db mice. These results suggested that ACE2 may regulate intramuscular fat accumulate in mice. |
Formal Description Interaction-ID: 116143 |
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Drugbank entries | Show/Hide entries for ACE2 |
Comment | ACE2 deficiency in vivo displayed lipid accumulation, ER stress and mitochondrial dysfunction in skeletal muscle. |
Formal Description Interaction-ID: 116929 |
gene/protein decreases_activity of phenotype |
Drugbank entries | Show/Hide entries for ACE2 |
Comment | The protein levels of GRP78, eIF2alpha, ATF4, and CHOP were all significantly up-regulated in the skeletal muscle of the ACE2 KO mice. |
Formal Description Interaction-ID: 120293 |
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Drugbank entries | Show/Hide entries for ACE2 or HSPA5 |