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Moscow

Department of Biological Sciences
biosci@uidaho.edu
phone: (208) 885-6280
fax:(208) 885-7905
Life Sciences South 252
875 Perimeter Drive MS 3051
Moscow, ID 83844-3051

Onesmo Balemba

Onesmo Balemba, Ph.D.


Office: LSS 259
Phone: (208) 885-8023
Email: obalemba@uidaho.edu
Mailing Address: University of Idaho
Dept. of Biological Sciences
875 Perimeter Drive MS 3051
Moscow, Idaho 83844-3051

College of Science
University of Idaho
Associate Professor

Campus Locations: Moscow
With UI Since 2008


  • Biography
    My research focuses on  the pathophysiology of diseases that affect gastrointestinal (GI) functions. My aim is to gain a better understanding of neuromuscular and immune system host responses in diabetes, and infectious diarrhea, and therapeutic strategies for these conditions.
  • Selected Publications

    2010

    • Balemba, O.B., Yogesh Bhattarai, Y., Chloe Stenkamp-Strahm, C., Mellau L.S.B. and. Mawe, G.M. 2010. The traditional anti-diarrheal remedy, Garcinia buchananii stem bark extract, inhibits propulsive motility and fast synaptic potentials in the guinea pig distal colon. Neurogastroenterol. & Motil. 22(12): 1332-39. Epub 2010 Aug 16.
    • Lavoie, B., Balemba, O.B., Godfrey, C., Watson, CA., Galya Vassilleva, G., Corvera, CU., Nelson, MT., and Mawe, GM. 2010. Hydrophobic bile salts inhibit gallbladder smooth muscle function via stimulation of GPBAR1 receptors and activation of KATP channels. J. Physiol. 588(Pt 17): 3295-305.

    2000 -2009

    • Balemba, O. B., Bartoo, A.C., Nelson, M.T., and Mawe, G.M. 2008. Role of mitochondria in spontaneous rhythmic activity and intracellular calcium waves in the guinea pig gallbladder smooth muscle.  Am. J. Physiol Gastrointest. Liver Physiol. 2008; 294 (2):G467-76.
    • Lavoie, B., Balemba, O. B., Nelson, M.T, Ward, S.M. and Mawe, G.M.  2007. Morphological and physiological evidence for interstitial cell of Cajal-like cells in the guinea pig gallbladder. J Physiol. 579 (Pt 2):487-501.
    • Balemba, O.B., Salter, M.J., Heppner, T.J., Bonev, A.D., Nelson, M.T. and Mawe, G.M.  2006. Spontaneous Electrical Rhythymicity and the Role of the Sarcoplasmic Reticulum in the Excitability of Guinea Pig Gallbladder Smooth Muscle Cells. Am J Physiol Gastrointest Liver Physiol. 290(4):G655-64.
    • Balemba, O.B., Hay-Schmidt, A., Assey, R.J., Kahwa, C.K.B., Semuguruka, W.D. and Dantzer, V. 2002. An immunohistochemical study of the organisation of ganglia and nerve fibres in the mucosa of the porcine intestine. Anatomia Histologia and Embryologia 31(4): 237-246.
    • Balemba, O.B., Semuguruka, W. D., Hay-Schmidt, A., Johansen, M.V. and Dantzer, V. 2001. Vasoactive intestinal peptide and substance P-like immunoreactivities in the enteric nervous system of the pig correlate with the severity of pathological changes induced by Schistosoma japonicum. International Journal for Parasitology 31(13): 1503-1514.
  • Research Projects
    • Anti-diarrhea remedy

      Diarrheal diseases are among the leading causes of illness and death of children and HIV/AIDS patients and a major symptom of stress.  There is wide range of the causative agents, and cellular mechanisms leading to the development of the symptoms of diarrhea are complexity and diverse.  Therefore, the effective treatment of diarrheal diseases requires more than one drug in order to alleviate the symptoms of increased motility, secretion and abdominal pain; to eliminate the etiological agent(s) and to treat the associated inflammation. There is need for new theraputic agents especially drugs that reduce enteric neurotransmission, which is the main factor underlying  increased bowel movements and abdominal discomfort/pain.

      Herbal extracts have been used for thousands of years to treat diarrhea, and still are widely used to treat diarrheal diseases. We are investigating  the efficacy of  extracts from the bark of Garcinia buchananii as anti-diarrheal  folk remedy of diarrheal disease, anti-inflammatory,  and analgesic activities effects. The long-term goal is to conduct thorough scientific investigations of the efficacy and safety of the extracts; isolate the bioactive components; and determine cellular mechanisms underlying actions related to anti-diarrhea, pain and inflammatory activity; and promote the use of extracts as an affordable natural herbal drug to treat diarrhea and associated pain and inflammation.


    • Obesity & Type 2 Diabetes Mellitus

      Obesity and type 2 diabetes mellitus studies in a mouse model

      Obesity and T2DM are metabolic diseases of major socioeconomic impact, morbidity and mortality. Worldwide, about one in every 10 adults are overweight and roughly 150 million people have T2DM. The risk factors for developing T2DM include: overweight, inactivity, genetic predisposition (family history and race) as well as aging. Cardinal features of T2DM are: obesity, insulin resistance, glucose intolerance, and low grade inflammation. Disease events originate in the gastrointestinal (GI) tract, and GI organs are a prime target for successful therapeutic intervention against obesity and T2DM. Recent studies indicate that the interaction between excessive calories and microorganisms in the GI tract, disrupted mucosal permeability, and chylomicron-mediated lipopolysaccharide (LPS) trans-epithelial transport causes endotoxemia. The latter induces fat deposition, inflammation and insulin resistance, the metabolic syndromes that ultimately develop into obesity and T2DM.

      Diabetic neuronal cell death and altered neurochemistry (neuropathy) occur in the enteric nervous system (ENS; the “little brain” in the gut) because it is morphologically and functionally similar to the brain) of humans and experimental animals. Neuropathy is considered to be a key factor underlying bowel disorders that are common among obese and T2DM patients.  New research data indicate that enteric neural mechanisms have a crucial role in the development and in the therapeutic interventions against obesity and T2DM. The role of the ENS in the pathophysiology of obesity and T2DM is not fully understood.  The first long-term goal of  our research program  is to gain a better understanding of how excessive caloric intake, especially the consumption of fatty acids disrupts neurotransmission, and causes injury and death of enteric neurons. The second goal of this research is to utilize anti-inflammatory neural mechanisms to protect the ENS and preserve mucosal-barrier function, thus controlling the metabolic endotoxemia. These investigations will enhance understanding of the pathogenesis of GI motility disorders  that are widespread in type 2 diabetics and  shed light on how the enteric neuromuscular axis can be protected from damages induced by excessive calories and subsequent metabolic syndromes.  These breakthroughs will contribute to the development of effective treatments of neurological disorders, improving quality of life of obese and T2DM patients.



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