“…Furthermore, one study found that 40% of patients with functional dyspepsia had slow small intestinal transit times and an increased likelihood of reporting bloating and abdominal pain (Chitkara et al, 2003). There are reports that gastrointestinal motility is regulated not only by nitric oxide (NO) (Kuo et al, 2009;Chen et al, 2010), and gastrointestinal peptides including gastrin (Modlin et al, 1997;Itoh, 1997), and ghrelin (Masuda et al, 2000;Inui, 2001;Asakawa et al, 2001), but also by various neurotransmitters such as 5-hydroxytryptamine (5-HT) (Mine et al, 1997;Takeda et al, 2008;Tominaga et al, 2011), dopamine (Cooper and McRitchie, 1985;Iwanaga et al, 1991;Li et al, 2006), catecholamines (Scheibner et al, 2002;Choudhury et al, 2009), and acetylcholine (Decktor et al, 1988;Fujii et al, 2002). Yamahara et al (1977) reported that an extract of Atractylodes lancea and a volatile component -eudesmol caused no gastrointestinal damage such as stress-induced stomach ulcers, the secretion of gastric juice, or changes in small intestinal motility in rodents, but Yamahara et al (1990) reported in 1990 that the extracts of Atractylodes lancea, and their volatile components -eudesmol and hinesol enhanced intestinal motility in mice.…”