黄芩茎皮提取物及其生物活性成分甘露黄酮、GB-2和黄芩黄酮可减弱肠道抑制性神经肌肉传递。

Q3 Medicine
Savannah Patterson, Michael Elder Waters, Nancy Braman, Roan Willson, Rodney A Hill, Jakob Magolan, Thomas Hofmann, Timo D Stark, Onesmo B Balemba
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引用次数: 0

摘要

Garcinia buchananii茎树皮提取物(GBB),通常用于治疗非洲腹泻,引发异位宫内收缩,导致体外结肠推进运动抑制。为了确定这些作用是否与抑制神经肌肉传递、相关成分化合物和作用机制有关,我们在豚鼠远端结肠中使用颗粒推进试验研究了GBB和从GBB中分离的特定组分和黄酮对肠道运动的影响。此外,采用微电极记录测量了对猪回肠和降结肠平滑肌抑制连接电位(IJPs)的影响。精神活性药物筛选程序二级受体功能测定用于确定GBB及其组成化合物是否通过嘌呤能(P2Y)和毒蕈碱受体起作用。GBB对推进性运动有抑制作用,但GBB的主要成分(2R,3S,2″R,3″R)-甘豆黄酮(MNF)、(2R,3S,2″R,3″R)-GB-2 (GB-2)和(2R,3S,2″S)-buchananiflavanone (BNF)对推进性运动没有影响。我们发现,在猪降结肠中,ijp含有嘌呤能、氮能和非嘌呤能非氮能成分。此外,回肠ijp是纯嘌呤能的。GBB阻断了ijp的所有成分,而MNF和GB-2仅抑制嘌呤能ijp。BNF抑制ijp的嘌呤能和非嘌呤能成分。MRS2365是一种Y1 (P2Y)激动剂,在GBB存在时不会引起持续的膜超极化。然而,GBB、MNF、GB-2和BNF不影响P2Y或毒蕈碱受体。综上所述,猪降结肠的抑制性神经肌肉传递涉及到ijp的所有成分。GBB可能通过MNF、GB-2和BNF的作用降低抑制性神经肌肉传递。这些作用不涉及P2Y或毒蕈碱受体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Garcinia buchananii stem bark extract and its bioactive constituents manniflavanone, GB-2 and buchananiflavanone attenuate intestinal inhibitory neuromuscular transmission.

Garcinia buchananii stem bark extract and its bioactive constituents manniflavanone, GB-2 and buchananiflavanone attenuate intestinal inhibitory neuromuscular transmission.

Garcinia buchananii stem bark extract and its bioactive constituents manniflavanone, GB-2 and buchananiflavanone attenuate intestinal inhibitory neuromuscular transmission.

Garcinia buchananii stem bark extract and its bioactive constituents manniflavanone, GB-2 and buchananiflavanone attenuate intestinal inhibitory neuromuscular transmission.

Garcinia buchananii stem bark extract (GBB), commonly used for treating diarrhea in Africa, triggers ectopic aboral contractions, causing inhibition of propulsive motility in the colon ex vivo. To determine whether or not these effects were associated with decreased inhibitory neuromuscular transmission, the responsible constituent compounds, and mechanisms of action, we studied the effects of GBB and specific fractions and flavanones isolated from GBB on intestinal motility using pellet propulsion assays in guinea pig distal colons. In addition, microelectrode recordings were used to measure the effects on the inhibitory junction potentials (IJPs) in the porcine ileum and descending colon smooth muscle. Psychoactive Drug Screening Program secondary receptor functional assays were used to determine whether or not GBB and its constituent compounds act via purinergic (P2Y) and muscarinic receptors. GBB inhibited propulsive motility, but (2R,3S,2″R,3″R)-manniflavanone (MNF), (2R,3S,2″R,3″R)-GB-2 (GB-2) and (2R,3S,2″S)-buchananiflavanone (BNF), the main ingredients of GBB, did not affect motility. We discovered that, in the porcine descending colon, IJPs contained purinergic, nitrergic, and nonpurinergic nonnitrergic components. Furthermore, ileal IJPs were purely purinergic. GBB blocked all components of IJPs, while MNF and GB-2 inhibited purinergic IJPs only. BNF inhibited the purinergic and nonpurinergic components of IJPs. MRS2365, a Y1 (P2Y) agonist, did not evoke sustained membrane hyperpolarization in the presence of GBB. However, GBB, MNF, GB-2 and BNF did not affect P2Y or muscarinic receptors. In conclusion, inhibitory neuromuscular transmission in the porcine descending colon involves all components of IJPs. GBB decreases inhibitory neuromuscular transmission, likely by the actions of MNF, GB-2 and BNF. These effects do not involve P2Y or muscarinic receptors.

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来源期刊
Journal of Smooth Muscle Research
Journal of Smooth Muscle Research Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
2.30
自引率
0.00%
发文量
7
审稿时长
10 weeks
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