Abstract:We administered 2.5 g of Shakuyaku-kanzo-to granule to 61 patients who had muscle cramp during hemodialysis (HD) sessions and examined its immediate effects. We selected 10 patients who wanted to take the drug at home, out of cases, for whom the drug was effective on the study described above and had them take the drug in the same way at the beginning of muscle cramp at home examined the effects. In the study during HD sessions, muscle cramp and its associated pain disappeared in 5.3 ± 3.9 min on average in 54… Show more
“…We found that the inhibitory effect of intraduodenally administered SKT and G. radix occurred within 15 min of administration, which is consistent with the reported onset of the clinical effect of SKT following oral administration (Hyodo et al, 2006). Further, six of the eight G. radix isolates (liquiritin apioside, liquiritigenin, isoliquiritin apioside, isoliquitirigenin, flavonoids; glycyrrhetinic acid, a triterpenoid; glycycoumarin, a coumarin derivative) followed a similar time course of inhibition as SKT and G. radix, suggesting that these were indeed the primary constituents of SKT with an antispasmodic effect.…”
Section: Discussionsupporting
confidence: 89%
“…Some of the precipitating factors include strenuous exercise, metabolic disorders, electrolyte disturbance, pregnancy, and iatrogenic causes such statins, diuretics, and immunosuppressants (Miller and Layzer, 2005). In Japan pharmacotherapy for muscle cramps includes muscle relaxants, anticonvulsants, vitamin and mineral supplements, and traditional Japanese herbal medicines (Kampo) such as shakuyakukanzoto (SKT) (Hinoshita et al, 2003;Hyodo et al, 2006). Most muscle relaxants and anticonvulsants, however, have untoward adverse effects of hepatotoxicity and central nervous system (CNS) depression, and those that directly target the skeletal muscles while sparing the CNS are scare (Richards et al, 2012).…”
“…We found that the inhibitory effect of intraduodenally administered SKT and G. radix occurred within 15 min of administration, which is consistent with the reported onset of the clinical effect of SKT following oral administration (Hyodo et al, 2006). Further, six of the eight G. radix isolates (liquiritin apioside, liquiritigenin, isoliquiritin apioside, isoliquitirigenin, flavonoids; glycyrrhetinic acid, a triterpenoid; glycycoumarin, a coumarin derivative) followed a similar time course of inhibition as SKT and G. radix, suggesting that these were indeed the primary constituents of SKT with an antispasmodic effect.…”
Section: Discussionsupporting
confidence: 89%
“…Some of the precipitating factors include strenuous exercise, metabolic disorders, electrolyte disturbance, pregnancy, and iatrogenic causes such statins, diuretics, and immunosuppressants (Miller and Layzer, 2005). In Japan pharmacotherapy for muscle cramps includes muscle relaxants, anticonvulsants, vitamin and mineral supplements, and traditional Japanese herbal medicines (Kampo) such as shakuyakukanzoto (SKT) (Hinoshita et al, 2003;Hyodo et al, 2006). Most muscle relaxants and anticonvulsants, however, have untoward adverse effects of hepatotoxicity and central nervous system (CNS) depression, and those that directly target the skeletal muscles while sparing the CNS are scare (Richards et al, 2012).…”
“…Based on this concept, several kinds of Kampo formula have been widely used for palliative care including cancer associated symptoms and adverse effect of chemotherapy in Japan 5) . SKT, a Kampo formulation with anticholinergic and prostaglandin inhibitory effect has been reported to be effective in reducing muscle pain, muscle spasms, joint pain and numbness 2,[6][7][8] . So, we first tried SKT for the treatment for the muscle cramps induced by S-1 administration.…”
Section: Discussionmentioning
confidence: 99%
“…Its incidence was reported only 0.2% in the treatment with S-1 1) . For the measure of this adverse event, it is reported that Shakuyaku-kanzo-to (SKT) a Kampo medicine could be effective 2) . In this report, we show the experience of the patient who was effective by the administration of Goshajinkigan (GJG) a different Kampo medicine to improve the muscle cramp arose by using S-1 for the treatment of pancreatic cancer.…”
We experienced a pancreatic cancer patient whose muscle cramp arose by using S-1 was improved by the administration of a Kampo formulation Goshajinkigan (GJG).Eighty-year-old female was diagnosed as having unresectable pancreatic cancer and then chemotherapy with S-1 and gemcitabine was initiated. After 4th course, gemcitabine had been discontinued by the toxicity, and then single administration for two weeks of a dose of 80 mg of S-1 was continued every three weeks. She often experienced muscle cramp at low legs, and she visited the emergency room with complaint of gait disturbance due to worse of muscle cramps. Her biochemical study showed almost normal electrolytes levels. Then a Kampo formulation Shakuyaku-kanzo-to (SKT), which was thought to be rapid-acting for these symptoms, was administered because of her sustained marked symptoms. No effect of SKT on these symptoms was observed; therefore, GJG was selected by Kampo medicine physician in combination with her complaints and body status. The administration of GJG was started 2.5 g once a day and then dose escalation was scheduled because it might induce gastrointestinal disorders. Since dose was escalated 5 g twice a day 2 weeks after initiation, incidence of muscle cramp was reduced three times a week. After 7 weeks, symptoms were disappeared. At this moment, she can continue the chemotherapy with S-1 under control of adverse event by the administration of 5 g of GJG twice a day.
“…Muscle cramp frequently develops under abnormal serum K + concentrations 4,11) during exerciseinduced dehydration 12) and hemodialysis 3,4) . These indicate the possible involvement of intra -and extracellular K + concentration charge in muscle cramps.…”
: Shakuyakukanzoto (shao -yao -gan -cao -tang) is a commonly used Chinese traditional herbal medicine for the treatment of acute pain with muscle cramp. However, its mechanism of action is unclear. We previously reported that a low concentration of Kanzo (licorice) and isoliquiritigenin, a component of licorice, inhibited the potassium (K + ) current in H9c2 cells. Therefore, in the present study, we examined the effects of Shakuyakukanzoto, Shakuyaku or Kanzo on the K + current (IKur) in H9c2 cells. Shakuyakukanzoto inhibited IKur in a concentrationdependent manner. The half -maximal concentration of Shakuyakukanzoto was approximately 1.3 mg/mL and the Hill coefficient was 1.2. The order of potency of inhibiting IKur was Kanzo> Shakuyaku kanzoto>Shakuyaku. Glycyrrhizin, a major component of licorice, had no inhibitory effect on IKur. A small interfering RNA experiment indicated that IKur was most likely to be Kv2.1 in H9c2 cells. Our results suggest that Shakuyakukanzoto may normalize intracellular and extracellular K + balance by inhibiting IKur and reducing K + efflux, while the Na + -K + pump promotes K + influx into myofibers. Consequently, excess K + may be reduced from external space of myofibers. This may be a part of the Shakuyakukanzoto mechanism for improving muscle pain.
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