We have derived equations, by employing [U-C-13] glucose and mass isotopome
r analysis, to determine the pathways of glycogen synthesis (J. Katz, W. P.
Lee, P. A. Wals, and E. A. Bergner. J. Biol. Chem. 264: 12994-13004, 1989)
. More recently, by use of these methods we have derived equations to deter
mine the rate of glucose recycling and of gluconeogenesis [Tayek and Katz.
Am. J. Physiol. 270 (Endocrinol. Metab. 33): E709-E717, 1996 and 272 (Endoc
rinol. Metab. 35): E476-E484, 1997, and Katz and Tayek. Am. J. Physiol. 275
(Endocrinol. Metab. 38): E537-E542, 1988]. The former equations have been
criticized and challenged by C. Des Rosiers, B. R. Landau, and H. Brunengra
ber [Am. J. Physiol. 259 (Endocrinol. Metab. 22): E757-E762, 1990], and the
latter recently by B. R. Landau, J. Wahren, S. F. Previs, G. K. Ekberg, D.
Yang, and H. Brunengraber [Am. J. Physiol. 274 (Endocrinol. Metab. 37): E9
54-E961, 1998]. Landau et al. claimed that our equations were in error and
"corrected" them. Their analysis, and their values for recycling and glucon
eogenesis (GNG) differ markedly from ours. We show here our equations and e
stimates of recycling and GNG to be correct. We present here a theoretical
analysis of recycling and discuss the determination of the Cori Cycle and G
NG. We illustrate by numerical examples the difference in parameters of glu
cose metabolism calculated by the methods of Katz and Landau. J. Radziuk an
d W. N. P. Lee [Am. J. Physiol. 277 (Endocrinol Metab. 40): E199-E207, 1999
] and J. K. Kelleher [Am. J. Physiol. 277 (Endocrinol. Metab. 40): E395-E40
0, 1999] present a mathematical analysis that, although differing in some r
espects from Landau's, supports his equation for GNG. We show in the APPEND
IX that their derivation of the equation for GNG is incorrect.