- About this Journal ·
- Abstracting and Indexing ·
- Aims and Scope ·
- Annual Issues ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
Evidence-Based Complementary and Alternative Medicine
Volume 2011 (2011), Article ID 823941, 6 pages
Acupuncture at “Zusanli” (St.36) and “Sanyinjiao” (SP.6) Points on the Gastrointestinal Tract: A Study of the Bioavailability of Tc-Sodium Pertechnetate in Rats
1Pós-Graduação de Ciências Médicas (PGCM), Universidade do Estado do Rio de Janeiro (UERJ), CEP: 20551-030, Rio de Janeiro, RJ, Brazil
2Departamento de BiofÍsica e Biometria, Instituto de Biologia Roberto Alcântara Gomes (IBRAG), UERJ, Brazil
3Academia Brasileira de Arte e Ciência Oriental/Colégio Brasileiro de Acupuntura (ABACO/CBA), Rio de Janeiro, Brazil
4Departamento de Ciências Fisiológicas, UERJ, Brazil
Received 30 January 2008; Accepted 23 December 2008
Copyright © 2011 Vasco Senna-Fernandes et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The objective of this study is to investigate the differences of acupuncture effect between the Zusanli (St.36) and Sanyinjiao (SP.6) points on the gastrointestinal-tract (GIT) segment performed by the bioavailability of Tc-sodium-pertechnetate (TcO4) in rats. Male Wistar rats (n = 21) were allocated into three groups of seven each. Group 1 was treated by acupuncture bilaterally at St.36; Group 2 at SP.6; and Group 3 was untreated (control). After 10 min of needle insertion in anesthetized rats, 0.3 mL of TcO4 (7.4 MBq) was injected via ocular-plexus. After 20 min, the exitus of animals was induced by cervical-dislocation and GIT organs isolated. However, immediately before the exitus procedure, blood was collected by cardiac-puncture for blood radio-labeling (BRL). The radioactivity uptake of the blood constituents was calculated together with the GIT organs by a well gamma counter. The percentage of injected dose per gram of tissue (%ID/g) of TcO4 was calculated for each GIT organs, while BRL was calculated in %ID. According to the one-way ANOVA, the stomach, jejunum, ileum from the treated groups (Group 1 and Group 2) had significant differences compared to the controls (Group 3). However, between the treated groups (Group 1 and Group 2), there were significant differences (P < .05) in the stomach, jejunum, ileum, cecum, transverse and rectum. In BRL analysis, Group 2 showed significant increase and decrease of the insoluble and soluble fractions of the blood cells, respectively (P < .0001). The authors suggest that St.36 may have a tendency of up-regulation effect on GIT, whereas SP.6, down-regulation effect. However, further rigorous experimental studies to examine the effectiveness of acupuncture in either acupuncture points need to be carried out.
The gastrointestinal tract (GIT) syndromes related to the pain and functional disorders are common in the general population and may be treated successfully by acupuncture [1, 2]. This type of therapy is regarded as one of the most acceptable complementary therapy in Western world since it might be explained under the scientific view .
In traditional Chinese medicine (TCM), Zusanli (St.36) point of “The Stomach Meridian of Foot-Yangming" and Sanyinjiao (SP.6) point of “The Spleen Meridian of Foot-Taiyin" are commonly used in human acupuncture to treat a wide range of health conditions, including GIT disorders such as stomach ache, abdominal pain and distension, constipation, diarrhea, vomiting, dysentery, indigestion and others [4–6].
In animal research, St.36 and SP.6 are frequently used to study acupuncture effects on various physiological regulatory mechanisms and control systems changes, including gastrointestinal disorders, gastrointestinal motor dysfunction, visceral pain, gastric secretions (alter acid secretion), gastric and intestinal motilities, and regulation of brain-gut peptides [7–12]. In spite of several categories of assessment methods were applied to investigate the neuromodulation actions on the GIT, the explanation of the mechanisms and effects of acupuncture on those organs and tissues remains unclear [1, 2, 13]. Probably, it is not totally controlled by central nervous system (CNS) . According to Kellow et al.  and Benarroch , all gastrointestinal reflexes that include ascending inhibitory reflexes (the rectocolonic and colonogastric reflexes), and descending excitatory reflexes (the gastrocolonic and ileocolonic reflexes) may also be controlled by the enteric nervous system (ENS). This system, regarded as the “Second Brain", provides capacity to induce GIT reflexes autonomously without any influence of the CNS.
In nuclear medicine, radionuclides such as are widely used to label molecular and cellular structures (radiopharmaceuticals or radiobiocomplexes). These labeled structures can be utilized to obtain scintigraphic images, or their bioavailability studies, which indicate the physiological processes including cells metabolism and circulation changes of a tissue .
The bioavailability of the radiobiocomplex -sodium pertechnetate (Na4) is applied in clinical nuclear medicine to detect some GIT conditions such as intestinal hemorrhages, Merckel's diverticulum disease, and ectopic gastric tissues . The unbound of pertechnetate anion () is distributed of throughout the vasculature and interstitial fluids by a slow diffusion mechanism, and it is concentrated in various organs including stomach and intestines . However, the bioavailability of NaO4 can be changed in many circumstances by intrinsic factors; blood flow, capillary permeability, membrane transport, intracellular interactions, biotransformation and others. Extrinsic factors include the radiobiocomplex quality, patient's health status, diseases states, drugs (natural or synthetic type), dietary, invasive medical procedures and complementary therapies as acupuncture [17–19].
The aim of this study was to investigate the differences of acupuncture effects stimulated at the acupoints St.36 and SP.6 on the GIT-organs performed by the bioavailability of NaO4 in male Wistar rats.
The experimental design was approved by the Ethical Committee of the Instituto de Biologia Roberto Alcantara Gomes, Universidade do Estado do Rio de Janeiro, under the guidelines on the use of living animals in scientific investigations. Twenty-one healthy albino male Wistar rats, weighing 250–350 g at between 4 and 5 months of age were randomly allocated into three groups of seven; in Group 1 (n = 7), rats were treated with acupuncture at St.36 bilaterally; in Group 2 (n = 7), rats were treated with acupuncture at SP.6 bilaterally; and Group 3 (n = 7), rats were untreated (control group).
2.2. Experimental Design
The rats were fasted overnight with free access to water and anesthetized with an intraperitoneal injection of sodium thiopental 6.7% (Thiopentax) at the dose of 60 mg/kg/ip, body weight. Rats were placed in a ventral decubitus position, without immobilization in order to avoid animal stress and to eliminate emotional factors .
In Group 1, all rats were treated by manual acupuncture by inserting 5 mm deep at St.36, bilaterally, with stainless needle measuring 0.25 × 20 mm of length with guide-tube (Sterile Acupuncture Needles Wujiang Shenli Medical and Health Material Co., Ltd, China) . In Group 2, animals received manual acupuncture by puncturing 5 mm deep into SP.6, bilaterally, with the same type of needle . These acupoints in rat was positioned according to the palpation of the anatomical location of the cutaneous sites described by various authors in previous studies [10, 12, 18–21], and assured with an analogical paquimeter (Sanny, Brazil). The St.36 acupoint was located at between the tibia and fibula, laterally to the distal end of the cranial tuberosity of the tibia, ~5 mm lateral to the anterior tubercle of the tibia, in the tibialis anterior muscle, innervated by the deep peroneal nerve [12, 19, 20]. The SP.6 acupoint was situated approximately 3 mm proximal the largest prominence of the medial malleolus at the posterior tibia, and in the space between the Achilles tendon and the distal part of the tibia [10, 18, 21]. The animals from Group 3 were free from treatment.
2.3. Bioavailability of Radiobiocomplex Procedure
After 10 min of needle insertion, a dose of 0.3 mL of NaO4 (7.4 MBq) consisted of pertechnetate Tc-99m () recently eluted from a column-type generator with the saline solution of 0.9% sodium chloride (Instituto de Pesquisas Energéticas e Nucleares, Comissão Nacional de Energia Nuclear, Brazil) was injected into the rat, via ocular plexus. The needles were withdrawn 20 min later, and the exitus of sedated animals was induced by cervical dislocation . The selected GIT organs comprised of stomach, duodenum, jejunum, ileum, cecum, transverse colon and rectum of each animal  were identified and removed surgically as follows. The stomach was resected at the segment between right before the cardiac sphincter and after pylorus sphincter. In the small intestine segment, three samples of the rat have been isolated; (i) 20 mm of the duodenum after pylorus, (ii) 20 mm of the jejunum of the middle distance of the SI, (iii) 20 mm of the ileum before the ileocolic valve. In the large intestine, another three samples were resected too, (iv) the cecum (blinc sac), (v) 20 mm of the transverse colon and (vi) 20 mm of the rectum. All internal gut content including chyme, intestinal secretions and feces was gently removed to avoid false radioactivity uptake results. Then, all GIT organs were weighted by an analytic balance (Bioprecisa, Electronic Balance, FA2104N, São Paulo, Brazil) (Figure 1).
2.4. Blood Labeling Method
Before the exitus of rat, 2 mL of blood sample was withdrawn into heparinized tube (0.2 mL of heparin) via cardiac puncture, between the fifth and sixth intercostal space of the rat's left hemithorax. Then, 1 mL of blood was processed by a centrifugator (Bio-Eng 4000—Indústria e Comércio Ltd., São Paulo, Brat room temperature in 5 min. The plasma (P) and blood cells (BC) were isolated. Following samples (20 μL) of P and BC were precipitated with 5% trichloroacetic acid whereas the soluble (S) and insoluble (I) fractions (F) of P and BC were determined. This procedure was used to assess the ability of the MA stimulation effects at St.36 and SP.6 on the blood constituents evaluated by blood labeling of NaO4 without using stannous chloride. Afterwards, the radioactivity of NaO4 uptake of all GIT organs and isolated blood constituents were measured by a gamma counter NaI (TI) (Cobra Auto-gamma, Packard Instrument Co.; Downers Grove, Illinois, USA). The percentage of injected dose of NaO4 per gram of tissue (%ID/g) of the GIT organs, were determined (Figure 1). The percentage of injected dose of NaO4 (%ID) of the blood constituents: P, BC, insoluble fractions of the plasma (IF-P) and blood cells (IF-BC), soluble fractions of the plasma (SF-P) and blood cells SF-BC was performed at the same time with the GIT organs samples  (Figure 1).
2.5. Statistical Analysis
For statistical analysis, the one-way ANOVA test, followed by the Tukey-Kramer Multiple Comparisons Test (TKMCT) were used in this study calculated the significant differences (P < .05). GraphPad InStat, version 3.01 and GraphPad Prism, version 3.00 (GraphPad Software Inc., San Diego Ca, USA) were applied to assess those tests.
Table 1 and Figure 2 show the statistical analyses carried out by the one-way ANOVA and TKMCT with significant differences of the radioactivity uptake in percentage of injected NaO4 dose per gram of organ (%ID/g) in GIT organs samples (stomach, jejunum, ileum, cecum, transverse colon, rectum) among three groups were significant (Table 1). According to one-way ANOVA, the stomach was the organ which had extremely significant increase of uptake among the groups. According to the intergroup study with TKMCT, in between the treated and control groups it was observed that stimulating St.36 manually (Group 1) with needle in rat induced significant increase of uptake (%ID/g) in stomach and in jejunum compared to the control (Group 3). While stimulating SP.6 (Group 2) in the same way in rat provoked significant decrease of uptake in ileum compare to the control (Group 3). Moreover, in between the treated groups (Group 1 and Group 2), there were significant differences in the stomach, jejunum, ileum, cecum and rectum, considering P < .05. However, duodenum was not significant among the groups (Table 1 and Figure 2).
3.2. Blood Labeling
Table 2 and Figure 3 show the radiolabeling of blood constituents. IF-BC and SF-BC could induce significant differences. Stimulating SP.6 manually (Group 1) could induce significant decrease of IF-BC and increase of SF-BC compared to the control (Group 3).
In Neuroscience, the somatovisceral reflex response, regarded as one of the neuromodulatory mechanisms of the autonomous nervous system, is suggested to be used to explain the actions of acupuncture through the relationship between acupoint and organ, empirically mentioned in the theory of Zang-Fu, in TCM [13, 19]. Cho et al.  pointed out that the acupuncture effects on the organs are generally mediated by CNS. Curiously, in our data (not included in this article) there were no significant difference of uptake of radioactivity in the brain among the groups (P > .05), which may let us speculate that CNS does not have full control on the body organs and tissues. Therefore, the relationship between the acupoints and zang-fu organs, described in TCM, may be explained by the ENS activities, since it can control directly the GIT organs responses without influences of CNS [5, 14, 15].
In this study, the authors did not use the “sham acupuncture" group as a useful “inactive" control, since the degree of inactivity with non-acupoints remains largely undetermined. Several authors suggested that the needling of non-acupoints could produce unpredictable physiological effects since the placement of the needle in any cutaneous location of the body surface would elicit biological responses (inflammatory reflex), and therefore could complicate the interpretation of the results in sham acupuncture [25–28]. Moreover, a supposed sham acupoint site may be confused to another acupoint which was not already discovered, or not including in this research. For instance, if a non-acupoint site is determined on 5 mm distal to St.36 in rat, it may correspond to another unexpected acupoint (Shangjuxu-St.37 or Tiaokou-St.38) which may induce specific radioactivity uptake.
In spite of the specificity of acupuncture is still questioned , in this research the actions of acupuncture at different acupoints in rat altered the bioavailability of TcO4 with significant differences of radioactivity uptake in some GIT organs [18, 19]. According to our data, the stomach, some parts of the small intestine (jejunum and ileum) and large intestine of Group 1 (St.36 acupuncture) showed significant increase of radioactivity uptake when compared with Group 2 (SP.6 acupuncture). We suggested that St.36 may have more capacity to promote activity than SP.6 in almost all segments of the GIT. When comparing the St.36-acupunture group (Group 1) with control (Group 3), we only observed that the uptake of radioactivity in the stomach and jejunum samples from Group 1 was significantly superior to Group 3. On the other hand, the data showed that there were lack of statistically significant differences between the treated and control groups (Group 1 versus Group 3 and Group 2 versus Group 3). However we could observe that all the mean values from Group 1 were higher than Group 3, whereas all from Group 2 were lower than Group 3. These results suggest that acupuncture stimuli at St.36 in rat may have an up-regulation tendency in various GIT organs, while at SP.6, a down-regulation tendency. These findings may be correlated to the excitatory and/or inhibitory responses or therapeutic potential actions promoted by these acupoints on different types of gastrointestinal functions or disorders referred in previous studies [2, 12, 30].
In acupuncture research on the specificity of the acupoints, imaging techniques such as single positron emission tomography, and functional magnetic resonance imaging have been used to investigate the sensorimotor pathways between the CNS and peripheral system of the GIT including the Brain-Gut Axis . These techniques could produce anatomical and/or physiological imaging by mapping changes in brain activity in response to sensory (acupuncture) stimuli , However, using the bioavailability of radiobiocomplexes, such as TcO4, to assess acupuncture effect, the potential actions of acupoints might be “quantified" by radioactivity uptake in the targeted organs which is directly related to the changes of the activity of these organs’ cells metabolism and blood circulation .
In the present study, St.36 and SP.6 under MA stimulation in rats showed that they may have potential therapeutic actions on some parts of GIT organs, which are thought to be useful not only to complementary-alternative therapies, but also to Western medicine. However, further rigorous experimental studies to examine their effectiveness in either acupuncture therapies need to be performed.
The authors would like to thank Dr. Sohaku Bastos, OMD, PhD, (Chairman of the Academia Brasileira de Arte e Ciência Oriental, Sohaku-In Foundation for Oriental Medicine, Brazil) and Conselho Nacional de Ciência e Tecnologia (CNPq) for helping and supporting this study. The authors also are grateful to Dr Marcos Antonio Borges, biologist from the “Laboratório de Hormónios—Setor de Endocrinologia—HUPE/UERJ", for his valuable effort in supervising the gamma counting management.
- Y.-P. Lin, S.-X. Yi, J. Yan, and X.-R. Chang, “Effect of acupuncture at Foot-Yangming Meridian on gastric mucosal blood flow, gastric motility and brain-gut peptide,” World Journal of Gastroenterology, vol. 13, no. 15, pp. 2229–2233, 2007.
- Y.-Q. Li, B. Zhu, P.-J. Rong, H. Ben, and Y.-H. Li, “Neural mechanism of acupuncture-modulated gastric motility,” World Journal of Gastroenterology, vol. 13, no. 5, pp. 709–716, 2007.
- S. X. Ma, “Neurobiology of acupuncture: toward CAM,” Evidence-Based Complementary and Alternative Medicine, vol. 1, pp. 41–47, 2004.
- Y. Li, G. Tougas, S. G. Chiverton, and R. H. Hunt, “The effect of acupuncture on gastrointestinal function and disorders,” American Journal of Gastroenterology, vol. 87, no. 10, pp. 1372–1381, 1992.
- X. N. Chen, Chinese Acupuncture and Moxibustion, Foreign Languages Press, Beijing, China, 1998.
- Y.-K. Yim, H. Lee, K.-E. Hong et al., “Electro-acupuncture at acupoint ST36 reduces inflammation and regulates immune activity in collagen-induced arthritic mice,” Evidence-Based Complementary and Alternative Medicine, vol. 4, no. 1, pp. 51–57, 2007.
- C.-S. Chang, J.-W. Chou, C.-W. Ko, C.-Y. Wu, and G.-H. Chen, “Cutaneous electrical stimulation of acupuncture points may enhance gastric myoelectrical regularity,” Digestion, vol. 66, no. 2, pp. 106–111, 2002.
- M. Choi, J. Jung, M. Seo et al., “Ultrasonographic observation of intestinal mobility of dogs after acupunctural stimulation on acupoints ST-36 and BL-27,” Journal of Veterinary Science, vol. 2, no. 3, pp. 221–226, 2001.
- H. U. Hecker, A. Steveling, E. P. Peuker, P. Kastner, and F. Liebchen, Color Atlas of Acupuncture: Body Points, Ear Points, Trigger Points, Thieme Press, New York, NY, USA, 2001.
- J. H. Kim, J. Y. Chung, Y. K. Kwon et al., “Acupuncture reduces alcohol withdrawal syndrome and c-Fos expression in rat brain,” American Journal of Chinese Medicine, vol. 33, no. 6, pp. 887–896, 2005.
- G. C. M. Sugai, A. O. Freire, A. Tabosa, Y. Yamamura, S. Tufik, and L. E. A. M. Mello, “Serotonin involvement in the electroacupuncture and moxibustion induced gastric emptying in rats,” Physiology & Behavior, vol. 82, pp. 855–861, 2004.
- A. Tabosa, Y. Yamamura, E. R. Forno, and L. E. Mello, “Effect of the acupoints ST-36 (Zusanli) and SP-6 (Sanyinjiao) on intestinal myoelectric activity of Wistar rats,” Brazilian Journal of Medical, vol. 35, pp. 731–739, 2002.
- A. Sato, “Neural mechanisms of autonomic responses elicited by somatic sensory stimulation,” Neuroscience and Behavioral Physiology, vol. 27, no. 5, pp. 610–621, 1997.
- J. E. Kellow, M. Delvaux, F. Azpiroz, M. Camilleri, D. G. Thompson, and E. M. M. Quigley, “Principles of applied neurogastroenterolgy,” in Rome II. The Functional Gastrointestinal Disorders: Diagnosis, Pathophysiology and Treatment; A Multinational Consensus, D. A. Drossman, E. Corazziari, N. J. Talley, W. G. Thompson, and W. E. Whitehead, Eds., pp. 191–156, Degon Associates, McLean, Va, USA, 2nd edition, 2000.
- E. E. Benarroch, “Enteric nervous system: functional organization and neurologic implications,” Neurology, vol. 69, no. 20, pp. 1953–1957, 2007.
- G. B. Saha, Fundamentals of Nuclear Pharmacy, Springer, New York, NY, USA, 5th edition, 2004.
- M. Bernardo-Filho, S. Santos-Fillho, E. G. Moura, A. I. Maiworm, M. M. C. Orlando, M. E. Penas, et al., “Drug Interaction with radiopharmaceuticals: a Review,” Brazilian Archives of Biology and Technology, vol. 48, pp. 13–27, 2005.
- D. E. De Souza, V. Senna-Fernandes, L. de Carvalho Brito, R. S. de Souza, D. França, C. V. Manoel, et al., “Acupuncture stimulation at sanyinjiao: effect on the sodium pertechnetate bioavailability in rats,” American Journal of Chinese Medicine, vol. 35, pp. 977–986, 2007.
- V. Senna-Fernandes, D. França, S. F. R. Moreno et al., “The effect of "Zusanli" (ST. 36) acupuncture on the bio-availability of sodium pertechnetate in Wister rats,” Acupuncture and Electrotherapeutics Research, vol. 31, no. 1-2, pp. 33–44, 2006.
- H. D. Zhao, L. N. Du, J. W. Jian, G. C. Wu, and X. D. Cao, “Neuroimmunal regulation of electroacupuncture (EA) on the traumatic rats,” Acupuncture and Electrotherapeutics Research, vol. 27, no. 1, pp. 15–27, 2002.
- B.-T. Choi, J. Kang, and U.-B. Jo, “Effects of electroacupuncture with different frequencies on spinal ionotropic glutamate receptor expression in complete Freund's adjuvant-injected rat,” Acta Histochemica, vol. 107, no. 1, pp. 67–76, 2005.
- R. R. Seeley, T. D. Stephens, and P. Tate, Essentials of Anatomy and Physiology, McGraw and Hill, New York, NY, USA, 4th edition, 2002.
- P. V. Capriles, A. P. Dias, T. E. Costa et al., “Effect of eggplant (Solanum melongena) extract on the in vitro labeling of blood elements with technetium-99 m and on the biodistribution of sodium pertechnetate in rats,” Cellular and Molecular Biology, vol. 48, no. 7, pp. 771–776, 2002.
- Z. H. Cho, E. K. Wang, S. H. Lee, and I. K. Hong, “Functional magnetic resonance imaging of the brain in the investigation of acupuncture,” in Clinical Acupuncture–Scientific Basis, G. Stux and R. Hammerschlag, Eds., pp. 83–95, Spring, New York, NY , USA, 2001.
- K. J. Tracey, “The inflammatory reflex,” Nature, vol. 420, no. 6917, pp. 853–859, 2002.
- F. Dincer and K. Linde, “Sham interventions in randomized clinical trials of acupuncture—a review,” Complementary Therapies in Medicine, vol. 11, no. 4, pp. 235–242, 2003.
- S. X. Ma, “Neurobiology of acupuncture: toward CAM,” Evidence-Based Complementary and Alternative Medicine, vol. 1, pp. 41–47, 2004.
- D. Ryan, “Toward improving the reliability of clinical acupuncture trials: arguments against the validity of 'sham acupuncture' as controls,” American Journal of Acupuncture, vol. 27, no. 1-2, pp. 105–109, 1999.
- A. Moore and H. McQuay, “Acupuncture: not just needles?” The Lancet, vol. 366, no. 9480, pp. 100–101, 2005.
- A. Tabosa, Y. Yamamura, E. Romão Forno, and L. E. A. M. Mello, “A comparative study of the effects of electroacupuncture and moxibustion in the gastrointestinal motility of the rat,” Digestive Diseases and Sciences, vol. 49, no. 4, pp. 602–610, 2004.
- Q. Aziz and A. G. Thompson, “Brain-gut axis in health and disease,” Gastroenterology, vol. 114, pp. 559–578, 1999.
- G. T. Lewith, P. J. White, and J. Pariente, “Investigating acupuncture using brain imaging techniques: the current state of play,” Evidence-Based Complementary and Alternative Medicine, vol. 2, no. 3, pp. 315–319, 2005.