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Protracted Hiccups Induced by Aripiprazole and Regressed after Administration of Gabapentin

机译:由阿里希哌唑诱导的伸长的打嗝并在施用加巴邦施用后回归

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Hiccups are sudden, repeated, and involuntary contractions of the diaphragm muscle (myoclonic contraction). It involves a reflex arc that, once activated, causes a strong contraction of the diaphragm immediately followed by the closure of the glottis translating into the classic “hic” sound. Hiccups can be short, persistent, and intractable depending on the duration. The most disabling hiccups often represent the epiphenomenon of a medical condition such as gastrointestinal and cardiovascular disorders; central nervous system (CNS) abnormalities; ear, nose, and throat (ENT) conditions or pneumological problems; metabolic/endocrine disorders; infections; and psychogenic disorders. Some drugs, such as aripiprazole, a second-generation antipsychotic, can induce the onset of variable hiccups. We describe herein the cases of three hospitalized patients who developed insistent hiccups after taking aripiprazole and who positively responded to low doses of gabapentin. It is probable that aripiprazole, prescribed at a low dosage (7.5?mg/day), would act as a dopamine agonist by stimulating D 2 and D 3 receptors at the “hiccup center” level—located in the brain stem—thus triggering the hiccup. On the other hand, gabapentin led to a complete regression of the hiccup probably by reducing the nerve impulse transmission and modulating the diaphragmatic activity. The present case series suggests the use of low doses of gabapentin as an effective treatment for aripiprazole-induced hiccups. However, our knowledge of the neurotransmitter functioning of the hiccup reflex arc is still limited, and further research is needed to characterize the neurotransmitters involved in hiccups for potential novel therapeutic targets.
机译:打嗝是突然的,重复的,和隔膜肌肉(肌阵挛性收缩)的不自主收缩。它涉及到一个反射弧,一旦被激活,导致紧接着声门翻译成经典的“嗝”声关闭膜片强烈收缩。打嗝可以根据持续时间很短,持续性,顽固性和。最禁用打嗝往往代表的医学病症如胃肠道和心血管疾病的附带现象;中枢神经系统(CNS)的异常;耳,鼻,喉(ENT)条件或pneumological问题;代谢/内分泌紊乱;感染;和心因性疾病。一些药物,例如阿立哌唑,第二代抗精神病药,可以诱导可变打嗝的发作。我们在此描述的谁服用阿立哌唑和谁积极回应低剂量的加巴喷丁的后发展坚持打嗝3名住院患者的病例。这是可能的阿立哌唑,在低剂量下规定的(小于〜7.5毫克/天),将通过在“打嗝中心”刺激d 2和d 3受体充当多巴胺激动剂电平位于脑干 - 因此引发打嗝。在另一方面,加巴喷丁可能通过降低神经冲动传递和调节膈肌活动导致打嗝的完全消退。本病例系列建议使用低剂量的加巴喷丁的作为一种有效的治疗阿立哌唑诱导的打嗝。然而,我们的打嗝反射弧神经递质功能的了解仍然有限,并且需要进一步的研究来表征参与打嗝潜在的新的治疗靶点的神经递质。

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