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Clenbuterol-induced muscle growth: investigation of possible mediation by insulin.

Abstract
The role of insulin as a possible mediator of the beta-adrenergic agonist stimulation of muscle growth was investigated. To exclude possible action of the beta-agonist on the pancreatic release of insulin, diabetes was induced in rats by a streptozotocin injection (100 mg/kg). Insulin levels were almost not detectable in these rats. Feeding either normal diet or diet containing the beta-adrenergic agonist clenbuterol (10 parts/million) did not alter plasma insulin concentrations. The effects of clenbuterol on muscle and weight gain were determined in diabetic rats given daily insulin replacement (D + I) and fed either a normal diet or clenbuterol-treated diet. Clenbuterol, fed for 1 wk, increased the wet weight of the gastrocnemius, soleus, and extensor digitorum longus muscles (15-23%) in both normal and D + I rats. Although clenbuterol increased body weight gain, it did not alter feed consumption and, therefore, feed efficiency (g gain/g food) was improved. Activities of cathepsin B and N-acetyl-beta-glucosaminidase, but not cathepsin D, were elevated in the soleus muscles of clenbuterol-treated rats. The clenbuterol-induced increase in muscle growth in the insulin-replaced diabetic rats indicated that this beta-adrenergic agonist effect was not mediated by an alteration of circulating levels of insulin, secondary to beta-agonist action on pancreatic insulin release.
AuthorsM A McElligott, J E Mulder, L Y Chaung, A Barreto Jr
JournalThe American journal of physiology (Am J Physiol) Vol. 253 Issue 4 Pt 1 Pg. E370-5 (Oct 1987) ISSN: 0002-9513 [Print] United States
PMID3310657 (Publication Type: Journal Article)
Chemical References
  • Blood Glucose
  • Ethanolamines
  • Insulin
  • Acetylglucosaminidase
  • Cathepsin B
  • Clenbuterol
Topics
  • Acetylglucosaminidase (metabolism)
  • Animals
  • Blood Glucose (metabolism)
  • Body Weight
  • Cathepsin B (metabolism)
  • Clenbuterol (pharmacology)
  • Eating
  • Ethanolamines (pharmacology)
  • Insulin (blood)
  • Male
  • Muscle Development
  • Muscles (enzymology)
  • Rats
  • Rats, Inbred Strains

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