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Research Article

Gynura procumbens ethanol extract improves vascular dysfunction by suppressing inflammation in postmenopausal rats fed a high-fat diet

ORCID Icon, , , , &
Pages 1201-1213 | Received 08 Feb 2021, Accepted 14 Aug 2021, Published online: 07 Sep 2021

Figures & data

Figure 1. Effects of Gynura procumbens extracts on systolic blood pressure of sham and postmenopausal (PM) groups at 0, 3 and 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05), bIndicates a significant difference compared to PM group (p < 0.05) and c indicates a significant difference compared PM + 250GP (p < 0.05).

Figure 1. Effects of Gynura procumbens extracts on systolic blood pressure of sham and postmenopausal (PM) groups at 0, 3 and 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05), bIndicates a significant difference compared to PM group (p < 0.05) and c indicates a significant difference compared PM + 250GP (p < 0.05).

Figure 2. Photomicrograph showing the section of aortic tissues in (A) Control; (B) 250GP; (C) 500GP; (D) ATV; (E) postmenopausal (PM); (F) PM + 250GP; (G) PM + 500GP and (H) PM + ATV after 6 months of supplementation where TI: tunica intima, TM: tunica media, TA: tunica adventitia and L: lumen under Verhoeff-Van Gieson stain. (LM × 40).

Figure 2. Photomicrograph showing the section of aortic tissues in (A) Control; (B) 250GP; (C) 500GP; (D) ATV; (E) postmenopausal (PM); (F) PM + 250GP; (G) PM + 500GP and (H) PM + ATV after 6 months of supplementation where TI: tunica intima, TM: tunica media, TA: tunica adventitia and L: lumen under Verhoeff-Van Gieson stain. (LM × 40).

Table 1. Aortic morphometric measurements of tunica intima (TI), tunica media (TM) and intima-media thickness (IMT) in sham and postmenopausal rats.

Figure 3. (A) Effects of Gynura procumbens extracts on aorta relaxation response induced by Ach in sham groups after 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05). (B) Effects of Gynura procumbens extracts on aorta relaxation response induced by Ach in postmenopausal groups after 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05). (C) Effects of Gynura procumbens extracts on aorta relaxation response induced by SNP in sham groups after 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05). (D) Effects of Gynura procumbens extracts on aorta relaxation response induced by SNP in postmenopausal groups after 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05). (E) Effects of Gynura procumbens extracts on aorta constriction response induced by PE in sham groups after 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05). ( F) Effects of Gynura procumbens extracts on aorta constriction response induced by PE in postmenopausal groups after 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05).

Figure 3. (A) Effects of Gynura procumbens extracts on aorta relaxation response induced by Ach in sham groups after 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05). (B) Effects of Gynura procumbens extracts on aorta relaxation response induced by Ach in postmenopausal groups after 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05). (C) Effects of Gynura procumbens extracts on aorta relaxation response induced by SNP in sham groups after 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05). (D) Effects of Gynura procumbens extracts on aorta relaxation response induced by SNP in postmenopausal groups after 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05). (E) Effects of Gynura procumbens extracts on aorta constriction response induced by PE in sham groups after 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05). ( F) Effects of Gynura procumbens extracts on aorta constriction response induced by PE in postmenopausal groups after 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05).

Figure 4. Effects of Gynura procumbens extracts on nitric oxide level in sham and postmenopausal (PM) groups at 0, 3 and 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control in month 3 (p < 0.05) and bIndicates a significant difference compared to control in month 6 (p < 0.05), cIndicates a significant difference compared to PM in month 3 (p < 0.05) and dIndicates a significant difference compared to PM in month 6 (p < 0.05).

Figure 4. Effects of Gynura procumbens extracts on nitric oxide level in sham and postmenopausal (PM) groups at 0, 3 and 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control in month 3 (p < 0.05) and bIndicates a significant difference compared to control in month 6 (p < 0.05), cIndicates a significant difference compared to PM in month 3 (p < 0.05) and dIndicates a significant difference compared to PM in month 6 (p < 0.05).

Figure 5. (A) Effects of Gynura procumbens extracts on IL-6 level in sham and postmenopausal groups at 0, 3 and 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05), cIndicates a significant difference compared to PM + 250GP (p < 0.05). (B) Effects of Gynura procumbens extracts on TNF-alpha level in sham and postmenopausal groups at 0, 3 and 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05), cIndicates a significant difference compared to PM + 250GP (p < 0.05). (C) Effects of Gynura procumbens extracts on CRP level in sham and postmenopausal groups at 0, 3 and 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05), cIndicates a significant difference compared to PM + 250GP (p < 0.05).

Figure 5. (A) Effects of Gynura procumbens extracts on IL-6 level in sham and postmenopausal groups at 0, 3 and 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05), cIndicates a significant difference compared to PM + 250GP (p < 0.05). (B) Effects of Gynura procumbens extracts on TNF-alpha level in sham and postmenopausal groups at 0, 3 and 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05), cIndicates a significant difference compared to PM + 250GP (p < 0.05). (C) Effects of Gynura procumbens extracts on CRP level in sham and postmenopausal groups at 0, 3 and 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05), cIndicates a significant difference compared to PM + 250GP (p < 0.05).

Figure 6. (A) Effects of Gynura procumbens extracts on sVCAM-1 level in sham and postmenopausal groups at 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05), cIndicates a significant difference compared to PM + 250GP (p < 0.05). (B) Effects of Gynura procumbens extracts on sICAM-1 level in sham and postmenopausal groups at 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05), cIndicates a significant difference compared to PM + 250GP (p < 0.05).

Figure 6. (A) Effects of Gynura procumbens extracts on sVCAM-1 level in sham and postmenopausal groups at 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05), cIndicates a significant difference compared to PM + 250GP (p < 0.05). (B) Effects of Gynura procumbens extracts on sICAM-1 level in sham and postmenopausal groups at 6 months of supplementation. Data are means ± SEM. aIndicates a significant difference compared to control (p < 0.05) and bIndicates a significant difference compared to PM group (p < 0.05), cIndicates a significant difference compared to PM + 250GP (p < 0.05).

Table 2. Effects of Gynura procumbens extract and atorvastation (ATV) supplementation on liver functions test in sham and postmenopausal (PM) groups at 0 and 6 months of study.

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Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation to any qualified researcher.