Department of Pharmacology and Toxicology, Michigan State University , East Lansing, Michigan.
Neuroscience Program, Michigan State University , East Lansing, Michigan.
Am J Physiol Gastrointest Liver Physiol. 2019 Jan 1;316(1):G132-G143. doi: 10.1152/ajpgi.00131.2018. Epub 2018 Oct 25.
The irritable bowel syndrome (IBS) is a functional gastrointestinal motor and visceral sensation disorder that is more common in women than men. Female serotonin transporter (SERT)-gene knockout (KO) rats exhibit hypersensitivity to colorectal balloon distention (CRD) that mimics colonic hypersensitivity occurring in female IBS patients. Alosetron (5-HT receptor antagonist) is used to treat diarrhea-predominant IBS in female patients. Other 5-HT receptor antagonists are ineffective at treating IBS symptoms. The visceromotor response (VMR) to CRD in SERT-KO and wild-type (WT) rats was measured following subcutaneous (sc), intracerobroventricular (icv), or intrathecal (it) treatment with 5-HT receptor antagonists and an agonist. Alosetron (sc) and granisetron (antagonists) caused a paradoxical increase in the VMR to CRD in SERT-KO female rats. Alosetron (sc) increased the VMR to CRD in WT male rats. Alosetron (it) increased the VMR to CRD in SERT-KO female rats only, and the 5-HT receptor agonist SR-52772 increased the VMR to CRD in SERT-KO male rats. Depletion of spinal 5-HT using 5,7-dihydroxytryptamine prevented the increase in VMR to CRD in SERT-KO female and male rats treated it with alosetron and SR-52772, respectively. Alosetron (icv) did not affect the VMR to CRD in WT or KO female rats, but it increased the VMR in male SERT-KO but not WT male rats. These data suggest that 5-HT receptor signaling at the dorsal spinal cord mediates visceral hypersensitivity in female SERT-KO rats. Such differences could facilitate development of sex-specific drug treatments for visceral pain. NEW & NOTEWORTHY We studied a model of female sex-specific visceral hypersensitivity using rats that had a loss of function of the serotonin transporter (SERT) caused by gene truncation. Female SERT-KO rats exhibited visceral hypersensitivity in response to colorectal balloon distention. We found that increased 5-HT signaling at dorsal spine 5-HT receptors was responsible for visceral hypersensitivity in female but not male SERT-KO rats.
肠易激综合征(IBS)是一种功能性胃肠道运动和内脏感觉障碍,在女性中比男性更为常见。雌性 5-羟色胺转运体(SERT)基因敲除(KO)大鼠对结直肠球囊扩张(CRD)表现出超敏反应,这种超敏反应类似于女性 IBS 患者中发生的结肠超敏反应。阿洛司琼(5-HT 受体拮抗剂)用于治疗女性腹泻型 IBS 患者。其他 5-HT 受体拮抗剂对治疗 IBS 症状无效。SERT-KO 和野生型(WT)大鼠的内脏运动反应(VMR)在皮下(sc)、脑室内(icv)或鞘内(it)给予 5-HT 受体拮抗剂和激动剂后进行测量。阿洛司琼(sc)和格兰司琼(拮抗剂)在 SERT-KO 雌性大鼠中引起对 CRD 的 VMR 反常增加。阿洛司琼(sc)增加了 WT 雄性大鼠对 CRD 的 VMR。阿洛司琼(it)仅增加 SERT-KO 雌性大鼠对 CRD 的 VMR,5-HT 受体激动剂 SR-52772 增加 SERT-KO 雄性大鼠对 CRD 的 VMR。用 5,7-二羟基色胺耗竭脊髓 5-HT 可防止分别用阿洛司琼和 SR-52772 治疗的 SERT-KO 雌性和雄性大鼠对 CRD 的 VMR 增加。阿洛司琼(icv)对 WT 或 KO 雌性大鼠对 CRD 的 VMR 没有影响,但增加了雄性 SERT-KO 大鼠但不增加 WT 雄性大鼠的 VMR。这些数据表明,背侧脊髓 5-HT 受体的 5-HT 受体信号转导介导了雌性 SERT-KO 大鼠的内脏超敏反应。这种差异可能有助于开发针对内脏疼痛的特定于性别的药物治疗。新的和值得注意的是我们使用因基因截断而导致 5-羟色胺转运体(SERT)功能丧失的大鼠研究了一种女性特有的内脏超敏反应模型。雌性 SERT-KO 大鼠对结直肠球囊扩张表现出内脏超敏反应。我们发现,背侧脊髓 5-HT 受体的 5-HT 信号增加是雌性而非雄性 SERT-KO 大鼠内脏超敏反应的原因。