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豆甾醇可能成为治疗神经紊乱的新型甾体药物:通过受体调节的 GABA 能机制的证据。

Stigmasterol can be new steroidal drug for neurological disorders: Evidence of the GABAergic mechanism via receptor modulation.

机构信息

Department of Pharmacy, University of Malakand, Chakdara, Dir (Lower), KPK, Pakistan.

Department of Pharmacy, University of Swabi, KPK, Pakistan.

出版信息

Phytomedicine. 2021 Sep;90:153646. doi: 10.1016/j.phymed.2021.153646. Epub 2021 Jun 30.

Abstract

BACKGROUND

Gamma-aminobutyric acid A (GABA) receptors have been implicated in anxiety and epileptic disorders.

HYPOTHESIS/PURPOSE: This study aimed to investigate the effects of stigmasterol, a plant sterol (phytosterol) isolated from Artemisia indica Linn on neurological disorders.

METHODS

Stigmasterol was evaluated on various recombinant GABA receptor subtypes expressed in Xenopus laevis oocytes and its anxiolytic and anticonvulsant potential was assessed using the elevated plus maze (EPM), light-dark box (LDB) test, and pentylenetetrazole- (PTZ-) induced seizure paradigms. Furthermore, computational modeling of α2β2γ2L, α4β3δ, and α4β3 subtypes was performed to gain insights into the GABAergic mechanism of stigmasterol. For the first time, a model of GABAδ subtype was generated. Stigmasterol was targeted to all the binding sites (neurotransmitters, positive and negative modulator binding sites) of GABA α2β2γ2L, α4β3, and α4β3δ complexes by in silico docking.

RESULTS

Stigmasterol enhanced GABA-induced currents at ternary α2β2γ2L, α4β3δ, and binary α4β3 GABAR subtypes. The potentiation of GABA-induced currents at extrasynaptic α4β3δ was significantly higher compared to the binary α4β3 subtype, indicating that the δ subunit is important for efficacy. Stigmasterol was found to be a potent positive modulator of the extrasynaptic α4β3δ subtype, which was also confirmed by computational analysis. The computational analysis reveals that stigmasterol preferentially binds at the transmembrane region shared by positive modulators or a binding site constituted by the M2-M3 region of α4 and M1-M2 of β3 at α4β3δ complex. In in vivo studies, Stigmasterol (0.5-3.0 mg/kg, i.p.) exerted significant anxiolytic and anticonvulsant effects in an identical manner of allopregnanolone, indicating the involvement of a GABAergic mechanism.

CONCLUSION

To our knowledge, this is the first study reporting the positive modulation of GABA receptors, anxiolytic and anticonvulsant potential of stigmasterol. Thus, stigmasterol is considered to be a candidate steroidal drug for the treatment of neurological disorders due to its positive modulation of GABA receptors.

摘要

背景

γ-氨基丁酸 A (GABA) 受体与焦虑和癫痫疾病有关。

假设/目的:本研究旨在研究从青蒿中分离得到的植物甾醇——豆甾醇对神经紊乱的影响。

方法

评估豆甾醇对在非洲爪蟾卵母细胞中表达的各种重组 GABA 受体亚型的影响,通过高架十字迷宫(EPM)、明暗箱(LDB)测试和戊四唑(PTZ)诱导的癫痫发作模型评估其抗焦虑和抗惊厥作用。此外,还对 α2β2γ2L、α4β3δ 和 α4β3 亚型进行了计算建模,以深入了解豆甾醇的 GABA 能机制。这是首次生成 GABAδ 亚型模型。通过计算机对接,豆甾醇靶向 GABAα2β2γ2L、α4β3 和 α4β3δ 复合物的所有结合位点(神经递质、正调节剂和负调节剂结合位点)。

结果

豆甾醇增强了三元 α2β2γ2L、α4β3δ 和二元 α4β3GABAR 亚型的 GABA 诱导电流。与二元 α4β3 亚型相比,豆甾醇对 extrasynaptic α4β3δ 诱导电流的增强作用显著更高,这表明 δ 亚基对效力很重要。研究发现豆甾醇是 extrasynaptic α4β3δ 亚型的有效正调节剂,这也通过计算分析得到了证实。计算分析表明,豆甾醇优先与正调节剂或由 α4 的 M2-M3 区域和 β3 的 M1-M2 组成的结合位点结合在 α4β3δ 复合物的跨膜区域。在体内研究中,豆甾醇(0.5-3.0mg/kg,ip)以与 allopregnanolone 相同的方式发挥显著的抗焦虑和抗惊厥作用,表明涉及 GABA 能机制。

结论

据我们所知,这是第一项报道豆甾醇对 GABA 受体的正向调节、抗焦虑和抗惊厥作用的研究。因此,由于豆甾醇对 GABA 受体的正向调节,它被认为是治疗神经紊乱的候选甾体药物。

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