Early Blood Glucose Responses to Konjac Glucomannan and Metformin in Alloxan-induced Diabetic Female Wistar Rats in Kenya: An Exploratory Study

Background: Konjac glucomannan (KGM) has been investigated for glycaemic modulation, but early responses to KGM, metformin, and their combinations remain insufficiently characterised in alloxan-exposed rats. Objective: To describe early blood glucose concentrations and within-animal changes among metformin, KGM, and combination-treated groups. Methods: Twenty-one female Wistar rats were allocated to seven groups (n = 3/group): one non-induced control group, two monotherapy groups, and four combination groups. Alloxan (130 mg/kg, intraperitoneally) was administered to Groups II–VII. Glucose concentrations at pretreatment baseline, 1.5 h, and 3 h were available for all animals; subsequent observation intervals differed by group. Group means, sample standard deviations, and 3-h within-animal changes were calculated. An exploratory one-way analysis of variance compared changes among the six alloxan-exposed groups. Results: Mean (SD) 3-h glucose concentrations in Groups I–VII were 7.57 (0.21), 13.27 (5.22), 20.97 (11.93), 5.73 (2.63), 6.57 (1.63), 16.77 (12.30), and 8.47 (1.20) mmol/L, respectively. Mean changes from baseline were +2.13, −7.37, −0.73, −7.10, −3.17, −3.67, and −1.47 mmol/L. The between-group analysis was not statistically significant, F(5, 12) = 1.755, p = .197. One combination-treated rat had a 3-h glucose concentration of 2.7 mmol/L. Conclusions: Unequal baseline concentrations, limited group sizes, the absence of an untreated diabetic control, and uncertain intermediate-dose assignments prevent causal inferences about comparative efficacy or pharmacological interactions. The observations are hypothesis-generating and highlight the need for controlled efficacy and safety studies.

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Journal
Journal of Advances in Medicine and Medical Research
Published
2026-10-29
DOI
https://doi.org/10.9734/jammr/2026/v38i116236
Primary Topic
Natural Antidiabetic Agents Studies
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article
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article

Early Blood Glucose Responses to Konjac Glucomannan and Metformin in Alloxan-induced Diabetic Female Wistar Rats in Kenya: An Exploratory Study

Shiundu Meshack, Gikunju Joseph, Akinyi Ochola Florence, Afuma Francis Maero et al.
Journal of Advances in Medicine and Medical Research
Natural Antidiabetic Agents Studies
article

Early Blood Glucose Responses to Konjac Glucomannan and Metformin in Alloxan-induced Diabetic Female Wistar Rats in Kenya: An Exploratory Study

Shiundu Meshack, Gikunju Joseph, Akinyi Ochola Florence, Afuma Francis Maero, Adem Samuel, Opii Omoite Joel, Ouma Brian, Omondi Collins
article en

Abstract

Background: Konjac glucomannan (KGM) has been investigated for glycaemic modulation, but early responses to KGM, metformin, and their combinations remain insufficiently characterised in alloxan-exposed rats. Objective: To describe early blood glucose concentrations and within-animal changes among metformin, KGM, and combination-treated groups. Methods: Twenty-one female Wistar rats were allocated to seven groups (n = 3/group): one non-induced control group, two monotherapy groups, and four combination groups. Alloxan (130 mg/kg, intraperitoneally) was administered to Groups II–VII. Glucose concentrations at pretreatment baseline, 1.5 h, and 3 h were available for all animals; subsequent observation intervals differed by group. Group means, sample standard deviations, and 3-h within-animal changes were calculated. An exploratory one-way analysis of variance compared changes among the six alloxan-exposed groups. Results: Mean (SD) 3-h glucose concentrations in Groups I–VII were 7.57 (0.21), 13.27 (5.22), 20.97 (11.93), 5.73 (2.63), 6.57 (1.63), 16.77 (12.30), and 8.47 (1.20) mmol/L, respectively. Mean changes from baseline were +2.13, −7.37, −0.73, −7.10, −3.17, −3.67, and −1.47 mmol/L. The between-group analysis was not statistically significant, F(5, 12) = 1.755, p = .197. One combination-treated rat had a 3-h glucose concentration of 2.7 mmol/L. Conclusions: Unequal baseline concentrations, limited group sizes, the absence of an untreated diabetic control, and uncertain intermediate-dose assignments prevent causal inferences about comparative efficacy or pharmacological interactions. The observations are hypothesis-generating and highlight the need for controlled efficacy and safety studies.

Journal of Advances in Medicine and Medical ResearchVol. 38(11)
Kenya Medical Training College (KE), Jomo Kenyatta University of Agriculture and Technology (KE)
Good health and well-being
Openalex Percentile: Top 11%
Natural Antidiabetic Agents Studies
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