Previous studies have been reported on the properties of moxa and the effect it has on the self defense mechanism of the body. To study the characteristics of acupoints, the study this time is from the point of whether there are any differences in biological responses if the same stimuli (5mg/body and 15mg/body of moxa) are applied to different acupoints. The acupoints chosen were KIMON, which is the therapeutic acupoint of liver, and DAIO, which is the spleen meridian acupoint located on the same vertical line and which has no effect on the liver. Male ddy mice (6 weeks old) were used as experimental animals. A comparison of the clinical biochemical values of serum 1, 3, 6 and 24 hours after application was conducted. The amount of invasion on body function from each moxibustion stimulus through the strength and progress of biological response was studied. Increases in serum Amylase, LDH, CK, GOT, and GPT in the DAIO group were obtained as compared to that of the KIMON group. There was also a decrease in serum CHE in the DAIO group as compared to that of the KIMON group. It was suggested that there were difference in biological responses between different application points, even with the application of the same stimuli.

In our previous studies, blood coagulation and fibrinolytic activity after single moxibustion were found to change within the range of physiological variability in mice. In this paper, the effect of multiple moxibustion on the activity of blood coagulation was examined by using male ddY mice (6 weeks old). 15mg of moxa was divided into 6 cones and mice were treated by each 3 cones at right and left LV-14. The multiple moxibustion schedule was a total of 5, 10 and 15 treatments. There was no effect of multiple moxibustion on body weight and Ht. 5 treatments of moxibustion showed a significant decrease in PT (p<0.05) and 10 treatments showed an increase in the ma value of TEG and in HPT activity. No significant change in PTT nor ATIII activity was found following multiple treatments of moxibustion.
These results showed that the enhancement of blood coagulation did not continue during multiple moxibustion even though single moxibustion stimulated the activity of blood coagulation at 1 and 3hrs. In addition, the increase in HPT activity induced by 10 treatments of moxibustion may have shown an effect of mildly stimulating liver function.

In our previous studies, it was suggested that single moxibustion stimulation activated blood coagulation and fibrinolytic activities within normal range in mice at 1 and 3hrs.
In order to further investigate the mechanism of moxibustion, we have examined the antithrombin III (AT III) and fibrinolytic activities after single moxibustion.
Male ddy mice (6 weeks old) were used as experimental animals. Each mouse was treated with 15mg of moxa divided into 6 cones, 3 each on the right and left LV-14.
We obtained the following results. The plasminogen (PLG) activities and the values of plasma total protein decreased at 1hr after single moxibustion.
The activities of plasma AT III, α2 plasmin inhibitor (α2 PI) and factor XIII, and plasma fibrinogen level remained unchanged at 1 and 3hrs.
The blood coagulation and fibrinolytic activities changed, but they were almost within the range of physiological variability.
These results suggest that blood coagulation and fibrinolysis were activated as part of its defence mechanism while keeping homeostatic balance.

The effect of moxibustion on the endocrinosis elicited by disorders of the autonomic nervous system was investigated in hypophysectomized rat.
Natural gain of body weight was stopped, adrenals and testis became atrophied, urinary output increased, and the rectal temperature slightly dropped after hypophysectomy.
Applying moxibustion did not correct these synptoms.
Furthermore, in spite of electrolyte and amino acid metabolism, significant decrease of Na, K, Cl, Ca and a slight decrease of urea nitrogen and creatinine in urine was recognized. But these were not modify by moxibustion.
With respect to the adrenal cortical study, there were a slight increase of 17-OHCS and a mild decrease of 17-KS in urine. Moxibustion did not effect either 17-OHCS or 17-KS.

The study reported here was undertaken to elucidate the action mechanism of moxibustion from the point of view of the blood coagulation and fibrinolytic activities.
Single stimulations at the right and left Chimen (KIMON) of male ddY strain 6 weeks old mice were made by using 15mg of moxa divided into 6 cones. Blood coagulation and fibrinolytic activities were determined at 1, 3, 24, 48, 72 and 168 (7 days) hours after moxibustion.
The increase of maximal amplitude (ma) of thrombelastography (TEG) and the reduction of coagulation time were observed during 1 to 168 hours. The increase of ma and the reduction of reaction time (r) of TEG at 1 and 3 hours, and reduction of plasma recalcification time at 24 hours, partial thromboplastin time at 3 hours and prothrombin time at 72 hours were significant compared with the values of intact normal mice. But these values of TEG and coagulation time were all in the normal range.
On the other hand, the increase of eugloblin lysis time (ELT) were observed at 1 hour, but at 3 to 168 hours, ELT values were reduced. And these activated tendency of plasminogen activator persisted for a period of 7 days.
These results suggest that the single moxibustion stimulation to Chimen induce some effect on the activities of some plasma proteins which concern the blood coagulation-fibrinolytic system.

In our previous studies, it was suggested that the single moxibustion stimulation induced the enhancement of the phagocytic activity in mice. In order to examine the cause of the effect of moxibustion, we have examined the activities of two lysosomal enzymes (acid phosphatase: acid-P and β-glucuronidase: β-Gl) in the peritoneal exudate cells (PEC) and peritoneal macrophage (Mp), and the morphological change of these cells by the Giemsa stain after single moxibustion.
Male ddY and ICR mouse (5-6 weeks old) were used as experimental animals. 15mg of moxa was divided into 6 cones and they were treated by each 3 cones at right and left LV-14.
As a result, an increase of acid-P activity in PEC of ddY mouse was found at 3 and 24hr after single moxibustion.
On the other hand, acid-P activity of PEC was decreased at 3hr, in spite of increase in numbers of PEC in ICR mouse.
These values did not change at 120hr after single moxibustion in ICR mice. But β-Gl activity in the peritoneal Mp was increased 120hr after single moxibustion.
Morphologically, there were a little enlarged and more mild spreading cells in peritoneal Mps from ICR mice 120hr after moxibustion than ones in untreated mice.
That is, lysosomal enzyme activities in PEC and peritoneal Mp increased when phagocytic indexes were higher by moxibustion stimulation in mice.
These results suggest that one of the cause of the enhancement of phagocytic activity in reticuloendothelial system after single moxibustion was the increase of lysosomal enzyme activities in the phagocytic cells.

In our previous report on mice, we suggested that single moxibustion stimulation to CHIMEN (LV-14) activated blood coagulation and fibrinolytic activity within normal range.
The purpose of this study is to elucidate the acute effects of moxibustion on blood coagulation activity in healthy adult men 1 and 3 hours after moxibustion. A single moxibustion stimulation to the right and left CHIMEN was made using a dose of 45mg of moxa divided into 30 cones.
The results were as follows:
1) decreased clot formation time (K) of thrombelastography 1 hour after moxibustion.
2) increased activity of hepaplastintest 3 hours after moxibustion.
3) decreased maximum value of platelet aggregation 1 and 3 hours after moxibustion.
4) decreased rate of segmented leucocyte and increased rate of lymphocyte 1 hour after moxibustion.
These results suggest that single moxibustion stimulation to CHIMEN have some influence on coagulation activity (the hepatic function on hepaplastintest), platelet aggregation and percentage of white blood cells.

Effects of multiple moxibustion on platelet aggregation, blood coagulation and fibrinolytic activity in mice have been studied. Male ddY mice (5 weeks old) were used as experimental animals. 15mg of moxa was divided into 6 cones and mice were treated by each 3 cones at right and left LV-14. The experimental schedules of multiple moxibustions were 5, 10 and 15 treatments of twice a week. The electronic aggregometer was suitable for measuring platelet aggregation using whole blood. However, no significant changes on platelet counts, platelet aggregation and ATP release induced by collagen (final concentration: 2μg/ml) and ADP (final concentration: 20μM) were found after multiple moxibustions. 15 treatments of moxibustion induced the increase in fibrinogen contents and the decrease tendency of factor XIII activity. While 10 treatments of moxibustion showed the increase in PLG content and α2 PI activity. These results suggested that multiple moxibustions induce the reasonable reaction to keep a good homeostasis on blood coagulation and fibrinolytic system in mice.

The purpose of this study was to analyze the relationship between activity pattern and temporal changes in the oxygen dynamics of human femoral medial vastus muscles. Oxygen dynamics were evaluated from the surface of the body by near-infrared spectroscopy (NIRS) . Arterial occlusion tests were performed in the femoral region at a cuff pressure of 300 mmHg. Exercise type and speed were controlled by CYBEX 6000. The exercise types examined were concentric contraction (CON) and eccentric contraction (ECC) . The 3 angular velocities of 90, 120 and 180 degrees were used as the exercise speeds. Exercise was performed continuously 60 times at maximum effort. The subjects were 7 healthy males with a mean age of 19.6±0.5 years. A transient decrease in oxygen concentration was observed during circulatory occlusion ; and rapid hyperemia occurred immediately after the removal of pressure. Oxygen concentration peaked above the control level and then returned to the initial level. In the CON exercise, the initial decrease in oxygen concentration was the largest at CON 90, and a gradual increase in oxygen concentration was clearly observed during exercise. In the recovery stage, after exercise at CON 90, 120 and 180, oxygen concentration exceeded the control level before exercise, then peaked and returned to the initial level. In the ECC exercise, an initial decrease in oxygen concentration was similar to that in the CON exercise, but a gradual increase in oxygen concentration was not observed during the exercise ; nor did oxygen concentration exceed the control level in the recovery stage after the exercise.
These results indicate that an increase in oxygen level after the removal of arterial occlusion, during and after the CON exercise was much higher than the control level before the exercise, sug-gesting the involvement of reactive hyperemia and exercise hyperemia.

Objective: Non-alcoholic fatty liver disease is common worldwide, and lifestyle modifications are key to its treatment. This study aimed to identify the barriers to lifestyle modifications in patients with non-alcoholic fatty liver disease and to organize the results using the Capability Opportunity Motivation-Behavior (COM-B) model.Materials and Methods: The framework of Arksey and O’ Malley was used in this scoping review. We searched PubMed, Scopus, and the Cochrane Library without language restrictions for reports published up to September 11, 2022, including peer-reviewed literature reporting barriers to lifestyle modifications in patients with non-alcoholic fatty liver disease. Patient-reported barriers were analyzed inductively and organized into the components (capability, opportunity, and motivation) of the COM-B model.Results: The literature search yielded 583 articles, of which seven qualitative studies, four quantitative studies, and one mixed-methods study met the inclusion criteria. Lack of time, lack of information on the diagnosis and management of non-alcoholic fatty liver disease, negative perceptions of the prescribed exercise and diet, physical symptoms interfering with the behavior, presence of comorbidities, and lack of family cooperation were frequently reported as barriers.Conclusion: The results of this study may contribute to the development of appropriate care and education strategies to promote behavioral changes in patients with non-alcoholic fatty liver disease.