Horsetail (Equisetum hyemale) Extract Accelerates Wound Healing in Diabetic Rats by Modulating IL-10 and MCP-1 Release and Collagen Synthesis

Traditionally, Equisetum hyemale has been used for wound healing. However, its mechanism of action remains to be elucidated. For this purpose, a 40% ethanolic extract of E. hyemale was prepared. Phytochemical screening revealed the presence of minerals, sterols, phenolic acids, flavonols, a lignan, and a phenylpropenoid. The extract reduced the viability of RAW 264.7 cells and skin fibroblasts at all times evaluated. On the third day of treatment, this reduction was 30–40% and 15–40%, respectively. In contrast, the extract increased the proliferation of skin fibroblasts only after 48 h. In addition, the extract increased IL-10 release and inhibited MCP-1 release. However, the extract did not affect both TGF-β1 and TNF-α released by RAW 264.7 cells. The higher release of IL-10 could be related to the up-/downregulation of inflammatory pathways mediated by the extract components associated with their bioactivity. The extract inhibited the growth of Staphylococcus aureus and Escherichia coli. Topical application of the extract accelerated wound healing in diabetic rats by increasing fibroblast collagen synthesis. These results suggest that E. hyemale extract has great potential for use in the treatment of wounds thanks to its phytochemical composition that modulates cytokine secretion, collagen synthesis, and bacterial growth.


Introduction
Plants of the genus Equisetum are used as herbal medicines in various regions of the world. About 20 species are naturally distributed throughout North America (Arctic Circle, Canada, United States, and Mexico), Mesoamerica, South America, Europe, and Northeast Asia to China, except for Australia and New Zealand [1]. The most common species in Mexico are E. arvense, E. hyemale, E. laevigatum, E. myriochaetum, and E. telmateia [1], and the most commonly used species is E. hyemale (horsetail, cola de caballo, kuture, or carricillo in Spanish) [2]. This plant is commercially available in herbariums and apothecaries and can be found along the banks of rivers and streams, in shallow water where the stem grows. E. hyemale is a herb up to two meters tall, with brittle, cylindrical hollow stems, unbranched, dark green, and spaced rings running around the stem, emerging from the joints. The fruits are small cones that are found in the terminal part of the plant [3]. This plant has been used in Mexico since pre-Columbian times as an astringent, anti-diabetic, diuretic, and for the treatment of kidney stones [4]. For these uses, the dry leaves and stems are prepared in an aqueous infusion. However, high concentrations of the raw plant material can cause adverse effects such as cardiac arrhythmias, muscle weakness, and erectile dysfunction, probably owing to its elevated thiaminase levels [2]. However, the fractionation by separation techniques avoids toxic reactions in mice [5]. Table 1. Chemical elements found in E. hyemale extract by X-ray fluorescence. Potassium (K), calcium (Ca), silicon (Si), chlorine (Cl), sulfur (S), phosphorus (P), iron (Fe), and magnesium (Mg). The minerals contained in the raw material are essential nutrients for the organism and are involved in several biological functions. For example, iron and magnesium are necessary for the regulation of acute and chronic inflammation and for the prevention of bacterial infections [19][20][21][22].

Thermal Analysis of Plant Extract
Thermogravimetric analysis (TGA) measures the loss of mass of each component of a mixture. It can provide an overview of water release and decomposition of the samples as a function of increasing temperature. Typical applications of TGA include the following: determining the thermal stability of a material; the purity of a mineral, inorganic compound, or organic material; improving product formulation processes; or ensuring product safety. TGA allows us to know the chemical composition and the interactions that the biomolecules of the extract establish to form a structure with amorphous order, and it also allows us to know the organic composition (bioactive molecules such as polyphenols, glycosides, and saponins) in % and the inorganic composition (minerals such as silicon, magnesium, and calcium oxides, mainly) also in %, in the extract of horsetail.
The TGA thermograms show three regions of mass loss: (1) evaporation of water and volatiles at 30 • C-110 • C, (2) endothermic decomposition of organic matter at 120-600 • C, and (3) formation of residual ash at 600-800 • C in the raw plant material and the E. hyemale extract ( Figure 1). Figure 1A shows the heat flux measured as a function of increasing temperature applied to the E. hyemale extract. The raw plant material contains a greater amount of water (8.2 ± 0.4%) and organic matter (65.3 ± 4.5%) than the extract (3.3 ± 1.0% and 47 ± 2.7%, respectively). A slow decrease in weight may indicate the presence of several volatile components in the region. In contrast, a rapid decrease in weight usually indicates the abundance of a particular component [23].
In general, plant extracts are a mixture of substances that interact with each other. In this sense, the decomposition of the extract can be associated with a wide variety of secondary metabolites, mainly phenolic, present in the extract [24]. The extract has a higher thermal stability than the raw plant material because the plant has fibers and increased hydrophilic components that can absorb moisture [25]. In addition, the E. hyemale extract contains a slightly higher residual ash mass (consisting of the elements analyzed by Xray fluorescence) than the raw plant material. These differences are probably due to the extraction process.
The first derivative analysis of the TGA thermogram shows that the raw material experiences a greater mass loss between 200 and 400 • C ( Figure 1B). The mass loss suffered by the samples can be interpreted as a loss of residual solvents, loss of hydration, or decomposition of organic matter [26]. There is also a higher formation of residual ashes between 600 and 800 • C, which is related to the high content of components and inorganic ions of the extracellular matrix of the plant. It is interesting to note that the extraction Pharmaceuticals 2023, 16, 514 4 of 23 process carried out allows for obtaining low-molecular-weight organic molecules that are decomposed between 150 and 200 • C, indicating that the ultrasound-/microwave-assisted extraction releases these agents from the plant matrix, obtaining a significant removal of the phytochemical components of the plant extracellular matrix.
Pharmaceuticals 2023, 16 In general, plant extracts are a mixture of substances that interact with each othe this sense, the decomposition of the extract can be associated with a wide variety of ondary metabolites, mainly phenolic, present in the extract [24]. The extract has a hi thermal stability than the raw plant material because the plant has fibers and incre hydrophilic components that can absorb moisture [25]. In addition, the E. hyemale ex contains a slightly higher residual ash mass (consisting of the elements analyzed by X fluorescence) than the raw plant material. These differences are probably due to the traction process.
The first derivative analysis of the TGA thermogram shows that the raw mat experiences a greater mass loss between 200 and 400 °C ( Figure 1B). The mass loss suff by the samples can be interpreted as a loss of residual solvents, loss of hydration, or composition of organic matter [26]. There is also a higher formation of residual ashes tween 600 and 800 °C, which is related to the high content of components and inorg ions of the extracellular matrix of the plant. It is interesting to note that the extrac process carried out allows for obtaining low-molecular-weight organic molecules tha decomposed between 150 and 200 °C, indicating that the ultrasound-/microwave-assi extraction releases these agents from the plant matrix, obtaining a significant remov the phytochemical components of the plant extracellular matrix.

Evaluation of Surface Crystallinity by X-Ray Diffraction
The X-ray diffraction (XRD) technique provides information on the structural s of powder samples, allowing the identification of crystalline, amorphous, and m phases. In the diffractogram of E. hyemale extract (Figure 2), X-ray diffraction peaks higher intensity were observed at angles 2θ = 28.1° and 40.5°, and peaks of a lower in sity were observed at angles of 21.2°, 29.6°, 30.6°, 43.5°, 50°, 59°, 66°, and 74°, indica that it has a crystalline structure. This can be related to the molecular diffusion phen

Evaluation of Surface Crystallinity by X-Ray Diffraction
The X-ray diffraction (XRD) technique provides information on the structural state of powder samples, allowing the identification of crystalline, amorphous, and mixed phases. In the diffractogram of E. hyemale extract (Figure 2), X-ray diffraction peaks of a higher intensity were observed at angles 2θ = 28.1 • and 40.5 • , and peaks of a lower intensity were observed at angles of 21.2 • , 29.6 • , 30.6 • , 43.5 • , 50 • , 59 • , 66 • , and 74 • , indicating that it has a crystalline structure. This can be related to the molecular diffusion phenomena that the extraction process regulates, in addition to the fact that the extracted molecular components can be related to each other, generating surfaces of a crystalline nature. On the other hand, in the diffractogram of the raw plant material, an amorphous halo centered at 22 • was observed, indicating that the presence of fibers reduces the surface crystallinity. The presence of biochemical and inorganic components allows the generation of surfaces of an amorphous nature in the raw material. Profiles similar to ours have been reported in other plants where it is mentioned that the peak around 15 • corresponds to an amorphous region. The peak around 22 • is attributed to crystalline regions related to the cellulose polymer, the main component of plant walls [25,27]. The crystalline structure of E. hyemale extract suggests that formulations prepared with the extract powder will be stable and have high bioavailability. Future experiments need to be conducted to address these issues.

Chemical Structure of E. hyemale Extract Evaluated by UV/Vis Spectrophotometry and Fourier Transform Infrared Spectroscopy (FTIR)
The UV/Vis absorption spectrum of E. hyemale extract shows two absorption bands between 230 and 270 nm and 340 and 380 nm and a maximum near 400 nm ( Figure 3A). The spectrum of gallic acid shows two absorption bands between 240 and 280 nm and 280 and 320 nm, while the spectrum of quercetin shows three absorption bands between 240 and 250 nm, 250 and 280 nm, and 340 and 410 nm ( Figure 3A). Typically, the UV/Vis absorption spectrum of flavonoids and phenolic acids is defined by two absorption bands between 300 and 380 nm and 240 and 280 nm intervals [28]. In this sense, the presence of both types of compounds is confirmed by these two characteristic bands in the UV/Vis spectrum of the extract ( Figure 3A). These absorption bands are associated with the movement of electrons from π orbitals (aromatic forms) to different molecular orbitals of characteristic energy.
Pharmaceuticals 2023, 16,x FOR PEER REVIEW to an amorphous region. The peak around 22° is attributed to crystalline regions to the cellulose polymer, the main component of plant walls [25,27]. The crystallin ture of E. hyemale extract suggests that formulations prepared with the extract pow be stable and have high bioavailability. Future experiments need to be conducted dress these issues.

Chemical Structure of E. hyemale Extract Evaluated by UV/Vis Spectrophotometry a Fourier Transform Infrared Spectroscopy (FTIR)
The UV/Vis absorption spectrum of E. hyemale extract shows two absorption between 230 and 270 nm and 340 and 380 nm and a maximum near 400 nm (Figu The spectrum of gallic acid shows two absorption bands between 240 and 280 nm and 320 nm, while the spectrum of quercetin shows three absorption bands betw and 250 nm, 250 and 280 nm, and 340 and 410 nm ( Figure 3A). Typically, the UV sorption spectrum of flavonoids and phenolic acids is defined by two absorption between 300 and 380 nm and 240 and 280 nm intervals [28]. In this sense, the pres both types of compounds is confirmed by these two characteristic bands in the spectrum of the extract ( Figure 3A). These absorption bands are associated with th ment of electrons from π orbitals (aromatic forms) to different molecular orbitals acteristic energy.

Chemical Structure of E. hyemale Extract Evaluated by UV/Vis Spectrophotometr Fourier Transform Infrared Spectroscopy (FTIR)
The UV/Vis absorption spectrum of E. hyemale extract shows two absorp between 230 and 270 nm and 340 and 380 nm and a maximum near 400 nm ( The spectrum of gallic acid shows two absorption bands between 240 and 280 n and 320 nm, while the spectrum of quercetin shows three absorption bands b and 250 nm, 250 and 280 nm, and 340 and 410 nm ( Figure 3A). Typically, the sorption spectrum of flavonoids and phenolic acids is defined by two absorp between 300 and 380 nm and 240 and 280 nm intervals [28]. In this sense, the p both types of compounds is confirmed by these two characteristic bands in spectrum of the extract ( Figure 3A). These absorption bands are associated with ment of electrons from π orbitals (aromatic forms) to different molecular orbit acteristic energy.  The FTIR (Fourier transform infrared spectroscopy) spectra ( Figure 3B) of the raw plant material and the E. hyemale extract are similar, and of these, the broad band between 3400 cm −1 and 3200 cm −1 corresponds to an O-H bond stretching vibration, indicating the presence of hydroxyl groups. These groups are attributed to the hydroxylated molecules (such as polyphenols) and their water content [6]. The presence of a band of lower intensity in the region between 2935 and 2915 cm −1 represents an N-H bond stretching vibration, indicating the presence of molecules with amino groups present in the plant extracellular matrix, as well as those corresponding to the C-H bond vibrations of the CH 2 group, typical of organic matter. The bands in the region between 1600 and 1475 cm −1 indicate the presence of C=C bonds, which are abundant in aromatic compounds with a phenyl nucleus. In the region between 1420 cm −1 and 1200 cm −1 , the band for the C-H bond bending vibration of methyl groups (-CH 3 ) and carboxylic acids is found.
Furthermore, the peaks between 1200 cm −1 and 1025 cm −1 are probably related to the presence of C-N amine groups, as observed in Figure 3B. The bands between 1000 and Pharmaceuticals 2023, 16, 514 6 of 23 900 cm −1 are related to the C-O-C bond vibrations of possible carbohydrates remaining in the extract. These results suggest that the extraction process does not alter the functional group content of the extract with respect to the raw plant material of E. hyemale. However, the intensity of the bands in the extract is higher than in the raw plant material, indicating a higher presence of bioavailable phytochemical compounds in the extract [29]. In addition, the release of these phytochemical components from the extracellular matrix of the plant by the extraction process promotes that these components have a higher vibration in the infrared than when they are trapped in the plant.
FTIR spectra of the gallic acid and quercetin standards were also obtained. Some similarities were observed between the spectra of the extract and these standards, especially in the regions consisting of OH groups, aromatic groups, carboxylic groups, and ether groups. However, other bands (800-1500 cm −1 ) were also observed in quercetin and gallic acid that were not observed in the extract, proving that they are components of lower polarity (hydrophobic) that are not extracted by the process used.

Total Polyphenol and Flavonoid Content in E. hyemale Extract
The content of total phenolic compounds in E. hyemale extract is 41.9 ± 2.4 mgEAG/g (mg equivalents of gallic acid per gram of sample), while the content of flavonoids is 5.5 ± 2.7 mgEQ/g (mg equivalents of quercetin per gram of sample). The phenolic compounds of E. arvense extract [30] are four times higher than those of E. hyemale. On the other hand, the concentration of flavonoids is similar to that found in E. arvense in Brazilian regions [7]. A variation in the concentrations of total polyphenols in E. hyemale could be due to the differences in the extraction procedures, the plant material used, as well as the different geographical locations of the Equisetum plants [7,31]. The gallic-acid-like phenolic and quercetin-like flavonoid compounds in E. hyemale suggest that the extract may have anti-inflammatory and antimicrobial activities similar to other Equisetum plants from different regions of the world.

Rt (min) m/z [M-H] -Identified Component
Family Structure 8.67 340.9 Caffeic acid 4-O-glucoside Hydroxycinnamic acids   (Table 3). Similar phytochemicals have been identified in E. hyemale fractions obtained with ethanol, methanol, diethyl ether, n-hexane, dichloromethane, and ethyl acetate using percolation, maceration, and ultrasound, in addition to caffeoyl tartaric acid, chlorogenic acid, cinnamic acid, luteolin, various flavones, unsaturated fatty acids, and carotenoids [5,7,13,39]. It is noteworthy that, with our extraction procedure (ultrasound and microwave), we identified phenol-2,4-bis(1-phenylethyl) and conidendrin, phenolic compounds that have never been reported in E. hyemale or other plants of the genus Equisetum. The presence of hydroxyl groups in the identified molecules allows their successful extraction, but not those with low polarity. The phenolic compounds identified in Mexican E. hyemale have pharmacological properties, including antimicrobial, antioxidant, anti-inflammatory, antiviral, and antimutagenic activity, among others.

Cells and Porcine Skin Fibroblasts
As expected, triton treatment (positive control) reduced the viability of the murine macrophage cell line, RAW 264.7 cells ( Figure 4A), and porcine skin fibroblasts by 80 and 60%, respectively ( Figure 4B). In RAW 264.7 cells, the E. hyemale extract reduced the cell viability by 30% to 60% at the three concentrations tested (0.6, 1.2, and 2.4 mg/mL) and at all times evaluated, but this effect was not dependent on the concentration or incubation time. On the other hand, the viability of porcine skin fibroblasts was significantly reduced (60-80%) at 24 and 48 h with all concentrations tested. However, after 72 h of treatment with the extract, fibroblast viability remained unchanged at the lowest concentration (0.6 mg/mL). At higher concentrations (1.2 and 2.4 mg/mL), the viability was reduced by only 30-40% compared with the control, suggesting that cytotoxicity on fibroblasts may depend on the incubation time. That is, low cytotoxicity can be observed with longer extract incubation times with the extract. Consistent with this, it has been reported that E. hyemale ethanolic extract has low cytotoxicity and maintains approximately 75% Vero cell viability at concentrations up to 12.5 mg/mL [40]. It has also been reported that E. hyemale extract inhibits L1210 cell proliferation by inducing G2/M arrest and cell apoptosis [41]. In addition, the ethyl acetate extract has a low toxicity in mice, causing mild changes in the liver without causing necrosis [5]. 35

Cells and Porcine Skin Fibroblasts
As expected, triton treatment (positive control) reduced the viability of the murine macrophage cell line, RAW 264.7 cells ( Figure 4A), and porcine skin fibroblasts by 80 and 60%, respectively ( Figure 4B). In RAW 264.7 cells, the E. hyemale extract reduced the cell viability by 30% to 60% at the three concentrations tested (0.6, 1.2, and 2.4 mg/mL) and at all times evaluated, but this effect was not dependent on the concentration or incubation time. On the other hand, the viability of porcine skin fibroblasts was significantly reduced (60-80%) at 24 and 48 h with all concentrations tested. However, after 72 h of treatment with the extract, fibroblast viability remained unchanged at the lowest concentration (0.6 mg/mL). At higher concentrations (1.2 and 2.4 mg/mL), the viability was reduced by only 30-40% compared with the control, suggesting that cytotoxicity on fibroblasts may depend on the incubation time. That is, low cytotoxicity can be observed with longer extract incubation times with the extract. Consistent with this, it has been reported that E. hyemale ethanolic extract has low cytotoxicity and maintains approximately 75% Vero cell viability at concentrations up to 12.5 mg/mL [40]. It has also been reported that E. hyemale extract inhibits L1210 cell proliferation by inducing G2/M arrest and cell apoptosis [41]. In addition, the ethyl acetate extract has a low toxicity in mice, causing mild changes in the liver without causing necrosis [5]. 39

Cells and Porcine Skin Fibroblasts
As expected, triton treatment (positive control) reduced the viability of the murine macrophage cell line, RAW 264.7 cells ( Figure 4A), and porcine skin fibroblasts by 80 and 60%, respectively ( Figure 4B). In RAW 264.7 cells, the E. hyemale extract reduced the cell viability by 30% to 60% at the three concentrations tested (0.6, 1.2, and 2.4 mg/mL) and at all times evaluated, but this effect was not dependent on the concentration or incubation time. On the other hand, the viability of porcine skin fibroblasts was significantly reduced (60-80%) at 24 and 48 h with all concentrations tested. However, after 72 h of treatment with the extract, fibroblast viability remained unchanged at the lowest concentration (0.6 mg/mL). At higher concentrations (1.2 and 2.4 mg/mL), the viability was reduced by only 30-40% compared with the control, suggesting that cytotoxicity on fibroblasts may depend on the incubation time. That is, low cytotoxicity can be observed with longer extract incubation times with the extract. Consistent with this, it has been reported that E. hyemale ethanolic extract has low cytotoxicity and maintains approximately 75% Vero cell viability at concentrations up to 12.5 mg/mL [40]. It has also been reported that E. hyemale extract inhibits L1210 cell proliferation by inducing G2/M arrest and cell apoptosis [41]. In addition, the ethyl acetate extract has a low toxicity in mice, causing mild changes in the liver without causing necrosis [5].  Figure 4B). In RAW 264.7 cells, the E. hyemale extract reduced the cell viability by 30% to 60% at the three concentrations tested (0.6, 1.2, and 2.4 mg/mL) and at all times evaluated, but this effect was not dependent on the concentration or incubation time. On the other hand, the viability of porcine skin fibroblasts was significantly reduced (60-80%) at 24 and 48 h with all concentrations tested. However, after 72 h of treatment with the extract, fibroblast viability remained unchanged at the lowest concentration (0.6 mg/mL). At higher concentrations (1.2 and 2.4 mg/mL), the viability was reduced by only 30-40% compared with the control, suggesting that cytotoxicity on fibroblasts may depend on the incubation time. That is, low cytotoxicity can be observed with longer extract incubation times with the extract. Consistent with this, it has been reported that E. hyemale ethanolic extract has low cytotoxicity and maintains approximately 75% Vero cell viability at concentrations up to 12.5 mg/mL [40]. It has also been reported that E. hyemale extract inhibits L1210 cell proliferation by inducing G2/M arrest and cell apoptosis [41]. In addition, the ethyl acetate extract has a low toxicity in mice, causing mild changes in the liver without causing necrosis [5].  It should be noted that 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) is reduced to formazan salts in mitochondria. This reduction depends on several factors: concentration, incubation time, number of viable cells, and mitochondrial metabolic activity. In this sense, the reduced viability found in RAW 264.7 cells and fibroblasts could also be due to the fact that adherent cells proliferate and growth is inhibited by contact so that mitochondrial metabolism (viability) can be reduced [42]. Our proliferation data support this idea, at least for fibroblasts. As shown in Figure 4 (C,E), the extract did not alter the proliferation rate of RAW 264.7 cells, indicated by red fluorescence. However, the extract increased the green fluorescence in skin fibroblasts, indicating a higher proliferation rate of this cell type ( Figure 4D,F). In both cases, triton treatment reduced the proliferation of both cell types, suggesting that skin fibroblasts are more sensitive than macrophages to some compounds of the extract that modulate biological targets involved in the viability or proliferation phenomena [43]. At this time, we do not identify the specific compound of the extract that mediates these effects on macrophage and fibroblast viability and proliferation. However, it has been shown that -sitosterol inhibits cell growth and cell cycle arrest of MCF-7 and A549 cells [44], phenol-2,4-bis(1-phenylethyl) inhibits human neutrophil migration [35], caffeic acid inhibits fibrosarcoma cell proliferation [45], kaempferol reduces fibroblast proliferation [46], and ferulic acid inhibits proliferation of RAW 264.7 cells [47]. In contrast, quercetin enhances fibroblast proliferation [48]. Cycloartenol and conidendrin have cytoprotective effects against cytotoxic stimuli in pancreatic and SH-SY5Y cells [49,50], and campesterol does not affect the RAW 264.7 cell viability [51]. Future work is needed to analyze the role of each component or their combinations. It should be noted that 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) is reduced to formazan salts in mitochondria. This reduction depends on several factors: concentration, incubation time, number of viable cells, and mitochondrial metabolic activity. In this sense, the reduced viability found in RAW 264.7 cells and fibroblasts could also be due to the fact that adherent cells proliferate and growth is inhibited by contact so that mitochondrial metabolism (viability) can be reduced [42]. Our proliferation data support this idea, at least for fibroblasts. As shown in Figure 4C,E, the extract did not alter the proliferation rate of RAW 264.7 cells, indicated by red fluorescence. However, the extract increased the green fluorescence in skin fibroblasts, indicating a higher proliferation rate of this cell type ( Figure 4D,F). In both cases, triton treatment reduced the proliferation of both cell types, suggesting that skin fibroblasts are more sensitive than macrophages to some compounds of the extract that modulate biological targets involved in the viability or proliferation phenomena [43]. At this time, we do not identify the specific compound of the extract that mediates these effects on macrophage and fibroblast viability and proliferation. However, it has been shown that γ-sitosterol inhibits cell growth and cell cycle arrest of MCF-7 and A549 cells [44], phenol-2,4-bis(1-phenylethyl) inhibits human neutrophil migration [35], caffeic acid inhibits fibrosarcoma cell proliferation [45], kaempferol reduces fibroblast proliferation [46], and ferulic acid inhibits proliferation of RAW 264.7 cells [47]. In contrast, quercetin enhances fibroblast proliferation [48]. Cycloartenol and conidendrin have cytoprotective effects against cytotoxic stimuli in pancreatic and SH-SY5Y cells [49,50], and campesterol does not affect the RAW 264.7 cell viability [51]. Future work is needed to analyze the role of each component or their combinations. Figure 5 shows the release of inflammatory mediators from RAW 264.7 cells stimulated with lipopolysaccharide (LPS). In this sense, treatment with E. hyemale extract did not affect the release of transforming growth factor-beta1 (TGF-β1) and TNF-α from RAW 264.7 cells at the times evaluated. However, the release of interleukin-10 (IL-10) was increased (threefold) only up to 72 h after stimulation with the extract, while the release of monocyte chemoattractant protein-1 (MCP-1) was decreased. It should be noted that the release of MCP-1 from control cells was fivefold higher at 72 h than at 24 h. This cytokine release pattern induced by the extract is not dependent on its concentration.  Figure 5 shows the release of inflammatory mediators from RAW 264.7 cells stimulated with lipopolysaccharide (LPS). In this sense, treatment with E. hyemale extract did not affect the release of transforming growth factor-beta1 (TGF-β1) and TNF- from RAW 264.7 cells at the times evaluated. However, the release of interleukin-10 (IL-10) was increased (threefold) only up to 72 h after stimulation with the extract, while the release of monocyte chemoattractant protein-1 (MCP-1) was decreased. It should be noted that the release of MCP-1 from control cells was fivefold higher at 72 h than at 24 h. This cytokine release pattern induced by the extract is not dependent on its concentration. IL-10 is a potent anti-inflammatory cytokine that facilitates wound healing by improving the transition from the inflammatory phase to the proliferative phase in injured tissue. It has also been documented that IL-10 reduces MCP-1 levels [52]. Under our experimental conditions, it is likely that MCP-1 levels were reduced by the increased release of IL-10. MCP-1 is a protein that attracts monocytes from the blood and macrophages from the tissue, releasing proinflammatory cytokines, thereby establishing a chronic inflammation and delaying the healing process. Therefore, it is convenient that E. hyemale extract inhibits the release of MCP-1. However, some evidence suggests that MCP-1 promotes wound epithelialization (proliferation phase) [52], so its release needs to be reduced but not completely inhibited. It is important to note that, although MCP-1 release from RAW 264.7 cells is reduced, its release is two times higher than after 24 h. These effects of E. hyemale extract on MCP-1 release may balance its low cytotoxic effect on macrophages and IL-10 is a potent anti-inflammatory cytokine that facilitates wound healing by improving the transition from the inflammatory phase to the proliferative phase in injured tissue. It has also been documented that IL-10 reduces MCP-1 levels [52]. Under our experimental conditions, it is likely that MCP-1 levels were reduced by the increased release of IL-10. MCP-1 is a protein that attracts monocytes from the blood and macrophages from the tissue, releasing proinflammatory cytokines, thereby establishing a chronic inflammation and delaying the healing process. Therefore, it is convenient that E. hyemale extract inhibits the release of MCP-1. However, some evidence suggests that MCP-1 promotes wound epithelialization (proliferation phase) [52], so its release needs to be reduced but not completely inhibited. It is important to note that, although MCP-1 release from RAW 264.7 cells is reduced, its release is two times higher than after 24 h. These effects of E. hyemale extract on MCP-1 release may balance its low cytotoxic effect on macrophages and its proinflammatory effect. These results suggest that E. hyemale extract may modulate the release of IL-10 and MCP-1 to facilitate faster wound healing. At this time, we do not know the specific compound responsible for these inflammatory mediator release profiles.

Effect of E. hyemale Extract on the Release of Inflammatory Mediators from RAW 264.7 Cells
However, we believe that cycloartenol, γ-sitosterol, phenol-2,4-bis(phenylethyl), flavonoids, and polyphenols contained in the E. hyemale extract may be involved. Flavonoids such as quercetin and kaempferol promote the secretion of anti-inflammatory cytokines and inhibit the release of inflammatory secretions through up-and downregulation of multiple pathways [53]. The role of campesterol in this effect seems unlikely as it does not alter IL-10 release from macrophages [54] or T lymphocytes [55].
On the other hand, TGF-β1 is a cytokine that induces the proliferation of fibroblasts and extracellular matrix proteins, favoring wound healing, and TNF-α is a potent proinflammatory cytokine that promotes the establishment of chronic inflammation [56]. In this sense, E. hyemale extract did not modify the TGF-β1 and TNF-α release in RAW 264.7 cells. Regarding TNF-α, low concentrations (below 30 pg/mL) were quantified in this work compared with other studies [57,58]. Only one study has reported similar concentrations [59]. These differences in the magnitude of the TNF-α concentration release could be due to, among other factors, incubation time, culture medium, cell line passage, treatment protocols, and regulation by other cytokines in the medium [60,61]. These results suggest that E. hyemale extract has anti-inflammatory properties by increasing the IL-10 release and inhibiting MCP-1 release at 72 h, without altering the release of TGF-β1 and TNF-α from RAW 264.7 cells.

Antimicrobial Activity of E. hyemale Extract
The antimicrobial activity of E. hyemale extract was evaluated against S. aureus (Grampositive) and E. coli (Gram-negative) ( Figure 6). Predictably, ceftriaxone induced a potent antimicrobial effect (minimum inhibitory concentration, MIC = 1 mg/mL) against both bacterial strains, as has been reported [66]. In addition, the E. hyemale extract inhibited the growth of S. aureus (MIC = 14.4 mg/mL) and E. coli (MIC = 27.6 mg/mL), with better potency against S. aureus than against E. coli.
Our results show that the extract from the Mexican E. hyemale has similar antimicrobial potency to the extract from the Brazilian plant (MIC = 13.1 mg/mL for both bacterial strains) [7,9], but better antimicrobial potency than the European Equisetum plant (MIC = 100 mg/mL for both strains) [67]. The separation technique, the solvents, and the growth zone of the plant influence the pharmacological efficacy of its bioactive compounds. For example, the extract from the Brazilian plant was obtained by maceration and using 70% v/v of ethanol. In this work, we used an ultrasound-/microwave-assisted extraction with 40% v/v ethanol, while the European extract was obtained with 70% v/v methanol. These differences could influence on the content of phenolic compounds (antioxidants) associated with the antimicrobial activity of E. hyemale extract [5][6][7][8], such as quercetin and kaempferol [7][8][9]67,68]. Curiously, the content of flavonoids is similar in both Mexican and Brazilian plants, suggesting that these bioactive compounds are responsible for their antibacterial activities. However, metallic elements such as iron and magnesium in the Mexican E. hyemale extract could also be involved in its antibacterial activity [22]. Our results show that the extract from the Mexican E. hyemale has similar antimicrobial potency to the extract from the Brazilian plant (MIC = 13.1 mg/mL for both bacterial strains) [7,9], but better antimicrobial potency than the European Equisetum plant (MIC = 100 mg/mL for both strains) [67]. The separation technique, the solvents, and the growth zone of the plant influence the pharmacological efficacy of its bioactive compounds. For example, the extract from the Brazilian plant was obtained by maceration and using 70% v/v of ethanol. In this work, we used an ultrasound-/microwave-assisted extraction with 40% v/v ethanol, while the European extract was obtained with 70% v/v methanol. These differences could influence on the content of phenolic compounds (antioxidants) associated with the antimicrobial activity of E. hyemale extract [5][6][7][8], such as quercetin and kaempferol [7][8][9]67,68]. Curiously, the content of flavonoids is similar in both Mexican and Brazilian plants, suggesting that these bioactive compounds are responsible for their antibacterial activities. However, metallic elements such as iron and magnesium in the Mexican E. hyemale extract could also be involved in its antibacterial activity [22].
Microbial infections delay wound healing and S. aureus is the major infecting strain. Therefore, it is relevant that E. hyemale extract has antimicrobial activity against this bacterium. However, the antimicrobial effects of E. hyemale extract occur at concentrations between 10 and 30 times higher than those with anti-inflammatory activity. Therefore, the next steps in the research of E. hyemale extract will focus on improving its antimicrobial potential. This challenge can be addressed by (1) improving the extraction process to concentrate the antimicrobial compounds [8,69], (2) combining the extract with compounds with high antimicrobial potency [70], and (3) incorporating the extract into polymeric matrices that enhance its antimicrobial properties [71]. After achieving the above, new studies are needed to investigate the antimicrobial activity of the extract on clinical isolates of bacterial strains of S. aureus, S. epidermis, P. aeruginosa, Streptococcus spp., and Enterococcus spp.

Effect of E. hyemale Extract on Wound Healing in Type 2 Diabetic Rats
Blood glucose levels were 103 ± 7 mg/dL in non-diabetic rats and 298 ± 17 mg/dL in diabetic rats on day 0. After 21 days, these levels were 105 ± 13 and 400 ± 18 mg/dL for non-diabetic and diabetic rats, respectively. The above values indicate the establishment and maintenance of type 2 diabetes in the animals studied. Figure 7 shows the time course of the wound-healing progress in Wistar rats. All experimental groups showed progressive wound reduction from day 3 to day 21. Visually, Microbial infections delay wound healing and S. aureus is the major infecting strain. Therefore, it is relevant that E. hyemale extract has antimicrobial activity against this bacterium. However, the antimicrobial effects of E. hyemale extract occur at concentrations between 10 and 30 times higher than those with anti-inflammatory activity. Therefore, the next steps in the research of E. hyemale extract will focus on improving its antimicrobial potential. This challenge can be addressed by (1) improving the extraction process to concentrate the antimicrobial compounds [8,69], (2) combining the extract with compounds with high antimicrobial potency [70], and (3) incorporating the extract into polymeric matrices that enhance its antimicrobial properties [71]. After achieving the above, new studies are needed to investigate the antimicrobial activity of the extract on clinical isolates of bacterial strains of S. aureus, S. epidermis, P. aeruginosa, Streptococcus spp., and Enterococcus spp.

Effect of E. hyemale Extract on Wound Healing in Type 2 Diabetic Rats
Blood glucose levels were 103 ± 7 mg/dL in non-diabetic rats and 298 ± 17 mg/dL in diabetic rats on day 0. After 21 days, these levels were 105 ± 13 and 400 ± 18 mg/dL for non-diabetic and diabetic rats, respectively. The above values indicate the establishment and maintenance of type 2 diabetes in the animals studied. Figure 7 shows the time course of the wound-healing progress in Wistar rats. All experimental groups showed progressive wound reduction from day 3 to day 21. Visually, the wounds showed no signs of excessive redness, irritation, or infection. In the nondiabetic control group treated with physiological saline solution (0.9%), the wound healed completely by day 21. However, delaying healing was observed in type 2 diabetic rats receiving the same treatment (wound slightly open on day 21). In fact, in this group, the wound did not close until day 28. On the other hand, daily application of the lowest concentration (0.6 mg/mL) of the extract did not accelerate the wound-healing process in diabetic rats, but the treatment with concentrations of 1.2 mg/mL and 2.4 mg/mL accelerated the healing process, as the wounds were closed completely on days 14 and 21, respectively.
The graph of wound healing as a function of time is shown in Figure 8A (wound contraction). On days 3, 7, 11, and 14, the healing process in diabetic rats was slower than in non-diabetic rats (treated with physiological saline solution). In fact, the percentage of wound contraction in diabetic rats on these days was approximately 50% less than in non-diabetic rats. On days 17 and 21, the rate of wound contraction in diabetic rats was still lower than in non-diabetic rats, although the contraction difference was only 13%. completely by day 21. However, delaying healing was observed in type 2 diabetic rats receiving the same treatment (wound slightly open on day 21). In fact, in this group, the wound did not close until day 28. On the other hand, daily application of the lowest concentration (0.6 mg/mL) of the extract did not accelerate the wound-healing process in diabetic rats, but the treatment with concentrations of 1.2 mg/mL and 2.4 mg/mL accelerated the healing process, as the wounds were closed completely on days 14 and 21, respectively. The graph of wound healing as a function of time is shown in Figure 8A (wound contraction). On days 3, 7, 11, and 14, the healing process in diabetic rats was slower than in non-diabetic rats (treated with physiological saline solution). In fact, the percentage of wound contraction in diabetic rats on these days was approximately 50% less than in nondiabetic rats. On days 17 and 21, the rate of wound contraction in diabetic rats was still lower than in non-diabetic rats, although the contraction difference was only 13%. Application of the extract at 0.6 mg/mL showed a tendency to accelerate the healing process in diabetic rats over time, although there was not statistically significant difference. Concentrations of 1.2 and 2.4 mg/mL of the extract significantly improved wound healing in type 2 diabetic rats, as wound contraction (30-40%) occurred similarly in non-diabetic rats on days 3, 7, and 11, but, from day 14 to 17, the wound contraction was better in diabetic rats treated with higher concentrations of the extract than in saline-treated non-diabetic and diabetic rats. The 1.2 mg/mL concentration of E. hyemale extract induced complete wound healing at 14 days, while the 2.4 mg/mL concentration did so up to 21 days. Although the highest concentration used induced faster wound healing than in diabetic rats treated with saline alone, we expected a reduction in the healing process less than 14 days, which did not occur. The simplest way to explain this phenomenon is that, as is the case with complex mixtures [72], the extract could exhibit hormetic responses (inverted U), whereby, at intermediate concentrations, the ratio of each component favors faster healing through a synergy between their phytochemicals.
After complete wound healing, the skin was harvested on days 21, 28, 24, 14, and 21 for the non-diabetic, diabetic control, and diabetic groups treated with 0.6, 1.2, and 2.4 mg/mL of the extract, respectively. Masson's trichrome staining revealed that the skin of nondiabetic and diabetic rats showed cell infiltrates and thin collagen bundles with a regular arrangement ( Figure 8B). However, in the skin of type 2 diabetic rats, the cell infiltrate was higher than in the skin of non-diabetic rats. In contrast, the collagen content was reduced ( Figure 8C), suggesting less migration of fibroblasts into the injured skin. Considering this, we believe that the cell infiltrates formed by a higher proportion of inflammatory cells, such as macrophages, lead to delayed healing in this group. On the other hand, the dermal layer of the healed skin of type 2 diabetic rats treated with the extract was similar to that of non-diabetic rats. However, some differences were observed. Regarding collagen deposition, the treatment with concentrations of 0.6 and 2.4 mg/mL ( Figure 8C) did not modify this parameter. Although the treatment with 1.2 mg/mL significantly increased the collagen content in the healed skin, treatment with 2.4 mg/mL of extract produced the most compact collagen layer. Cell infiltration in the skin of rats treated with 0.6, 1.2, and 2.4 mg/mL of the extract appeared to be higher than that of non-diabetic rats, but lower than that of diabetic rats treated with physiological saline alone. These results suggest that treatment with E. hyemale extract accelerates skin healing in type 2 diabetic rats by promoting the migration of fibroblasts into the damaged tissue. The main limitation of the present work is that histological analysis was performed on the skin of type 2 diabetic rats treated with the extract until the wound was completely healed. Future work must be performed at different times after wounding to know specific changes in the healing phenomenon induced by the extract of E. hyemale. Application of the extract at 0.6 mg/mL showed a tendency to accelerate the healing process in diabetic rats over time, although there was not statistically significant difference. Concentrations of 1.2 and 2.4 mg/mL of the extract significantly improved wound healing in type 2 diabetic rats, as wound contraction (30-40%) occurred similarly in nondiabetic rats on days 3, 7, and 11, but, from day 14 to 17, the wound contraction was better in diabetic rats treated with higher concentrations of the extract than in saline-treated nondiabetic and diabetic rats. The 1.2 mg/mL concentration of E. hyemale extract induced complete wound healing at 14 days, while the 2.4 mg/mL concentration did so up to 21 days. Although the highest concentration used induced faster wound healing than in diabetic rats treated with saline alone, we expected a reduction in the healing process less than 14 days, which did not occur. The simplest way to explain this phenomenon is that, as is the case with complex mixtures [72], the extract could exhibit hormetic responses (inverted U), whereby, at intermediate concentrations, the ratio of each component favors faster healing through a synergy between their phytochemicals.
After complete wound healing, the skin was harvested on days 21, 28, 24, 14, and 21 for the non-diabetic, diabetic control, and diabetic groups treated with 0.6, 1.2, and 2.4 Some flavonoids and γ-sitosterol have been shown to have potential as wound-healing agents [73][74][75][76][77]. The wound-healing properties of quercetin, caffeic and ferulic acids, and campesterol are related to the modulation of inflammatory cytokines and enhancement of fibroblast proliferation [78][79][80] via the Wnt/β-catenin signaling pathway [48,78]. In addition, cycloartenol [81] and γ-sitosterol promote collagen synthesis and fibroblast migration into injured tissue [76,77], whereas kaempferol delays healing by inhibiting the TGF-β1 receptor [46]. On this basis, it is likely that quercetin, γ-sitosterol, campesterol, Finally, from a simple perspective, a potential wound-healing treatment must reduce the viability/function of macrophages (to modulate the inflammatory phase of wound healing) and increase the proliferation of the fibroblasts (to accelerate the proliferative and remodeling phases) in the injured tissue. The E. hyemale extract meets these requirements. However, some negative reactions may occur with the topical application of the extract, so it is recommended not to use the horsetail extract in the case of suspected hypersensitivity to some of the active ingredients such as phenolic acids, flavonols, and sterols.

Chemical Reagents and Materials
The compounds used in this study were gallic acid (3,4,5-

Plant Material
Equisetum hyemale var. affine (Engel) A.A Eaton plant (horsetail, carricillo) was collected in July 2020, within the borders of the states of Jalisco and Zacatecas, Mexico (21 • 15 12.2 N 102 • 52 07.1 W). Certified botanists identified the plant and a specimen was deposited in the Luz María Villarreal de Puga Herbarium (voucher SIS-TRA-2020-03). The stem of the plant was dried in an oven at a temperature of 45 • C for 48 h and pulverized until a fine powder with a homogeneous particle size was obtained.

Elemental Analysis of Raw Plant Material by X-ray Fluorescence (XRF)
Elemental analysis of the raw plant material was performed by the X-ray fluorescence (XRF) method in a Malvern-PANalytical X-ray spectrometer at a voltage of 40 kV and a current of 30 mA, with a CuKα X-ray source (λ = 1.54 Å).

Extraction Procedure
For this, we used the powder obtained from the plant raw material in an ethanolic solution in a ratio of 1:10 (powder-solvent). Briefly, the extraction was performed with 80 g of powder and 800 mL of 40% v/v ethanol in a 1 L reactor. The reactor was connected to an ultrasound and microwave cooperative workstation (ATPIO Instruments Manufacture Co., Ltd., Nanjing, China). The instrument was operated in ultrasound mode at an amplitude of 25 KHz with a power of 99% at 28 • C. In microwave mode, the device was operated at 800 W and 50 • C. The equipment was operated simultaneously for 30 min. The extract was Pharmaceuticals 2023, 16, 514 16 of 23 filtered and then dried at room temperature. The extract was stored frozen (−20 • C) until use. Three different lots were used for phytochemical screening and biological activities.

Thermogravimetric Analysis (TGA) of Raw Material and Extract
The analysis of the raw material of the plant and the extract was carried out using a thermogravimetric analyzer (TGA-4000, Perkin Elmer, Shelton, CT, USA). The operating conditions used were a temperature range of 30 to 800 • C, a heating rate of 20 • C/min, and the use of nitrogen as an inert atmosphere up to 600 • C (20 mL/min); subsequently, a change from a gaseous atmosphere to oxygen was made to accelerate the exothermic decomposition of the analyzed samples up to 800 • C (20 mL/min).

X-ray Diffraction (XRD) Evaluation of the Raw Material and Extract
X-ray scattering measurements were performed on the extract and raw plant material of E. hyemale using Malvern-PANalytical equipment (Malvern, Worcs, UK) at a voltage of 40 kV and a current of 30 mA, with a CuKα X-ray source (λ = 1.54 Å) in the 2θ range from 10 to 80 • .

UV/Vis Spectrophotometry and Fourier Transform Infrared Spectroscopy (FTIR) Analysis of the Extract
The extract of E. hyemale (10 mg/mL) dissolved in water was scanned with a spectrophotometer (Metash Instruments Co. Ltd, Shangai, China) at a wavelength of 200 to 700 nm. Gallic acid and quercetin standards (10 mg/mL) were used for comparison. On the other hand, infrared analysis of raw plant material, E. hyemale extract, and gallic acid and quercetin standards was performed. Frontier equipment (Perkin Elmer, Shelton, CT, USA) was used, and the spectra were recorded with an attenuated total reflectance (ATR) accessory, with a resolution of 16 cm −1 in the range of 4000 to 650 cm −1 , using an average of 16 scans.

Quantification of Total Polyphenols and Flavonoids in the Extract
Quantification of total polyphenols in the extract was performed according to the modified Folin-Ciocalteu method. For this, 10% v/v Folin-Ciocalteu reagent, 2% w/v Na 2 CO 3 solution, and a 10 mg/mL solution of the extract in water were prepared. A 96-well microplate was filled with 40 µL of the extract, 80 µL of 2% w/v sodium carbonate, and 100 µL of the Folin-Ciocalteu reagent. The mixture was incubated for 15 min at room temperature. The absorbance of the sample was measured at 765 nm in a Sinergy HTX spectrophotometer (Fisher Scientific, Waltham, MA, USA). A modified aluminum chloride colorimetric method was used to determine the flavonoid content. For this purpose, 0.1 mL of a solution of 10 mg/mL of the extract in water, 1.4 mL of water, and 0.50 mL of the flavonoid reagent were mixed. The flavonoid reagent was prepared with 133 mg of aluminum chloride and 400 mg of sodium acetate in 100 mL of the solvent (140 mL of methanol, 50 mL of water, and 10 mL of acetic acid). Once the solutions were prepared, a volume of 200 µL of each sample or standard were transferred to a 96-well microplate and kept at room temperature for 30 min. Absorbance was measured at 430 nm in a Sinergy HTX spectrophotometer (Fisher Scientific, Waltham, MA, USA). A standard curve was constructed for gallic acid (7.8, 15.6, 31.3, 62.5, 125, 250, and 500 µg/mL) and quercetin (7.8, 15.6, 31.3, 62.5, 125, 250, 500, and 1000 µg/mL). Total polyphenols and flavonoids were expressed as mg gallic acid or quercetin equivalents per gram of sample (mgE/g), respectively. Three different lots were analyzed and three replicates of each lot were performed.
3.9. Identification of Components of the Extract by Chromatography 3.9.1. Gas Chromatography (CG-MS) Chromatographic analysis was carried out on a Varian ® Gas chromatography system (CP3800; Varian Inc., Walnut Creek, CA, USA) coupled with a Saturn 200 mass spectrometer (Varian Inc., Walnut Creek, CA, USA). The HP-5 MS column with a film thickness of 0.25 µm (30 m × 0.25 mm) was used for separation. The carrier gas was helium at a flow rate of 1 mL/min. The temperature of the injector and detector was 250 • C. MS detector parameters were transferred at a line temperature of 290 • C, with a solvent lag of 3 min. MS was performed in scan mode (m/z 40-600) for qualitative analysis. The identities of the components of the extract were assigned by the comparison of their retention times and mass spectra fragmentation patterns with those stored in the computer kit library, the NIST mass spectra library, and the published literature. Three different lots were analyzed. Creek, CA, USA) were used for reverse-phase highperformance liquid chromatography analysis, as previously reported [82]. Briefly, a liquid chromatograph ion trap mass spectrometer (Varian 500-MS IT Mass Spectrometer, Walnut Creek, CA, USA) equipped with an electrospray ion source was also used. Samples (5 µL) were injected onto a Denali C18 column (150 mm × 2.1 mm, 3µm, Grace, ND, USA). The oven temperature was maintained at 30 • C. The eluents were formic acid (0.2% v/v; solvent A) and acetonitrile (solvent B). The following gradient was applied: initial, 3% v/v B; 0-5 min, 9% v/v B linear; 5-15 min, 16% v/v B linear; 15-45 min, 50% v/v B linear. The column was then washed and reconditioned. The flow rate was maintained at 0.2 mL/min and elution was monitored at 245, 280, 320, and 550 nm. The whole effluent (0.2 mL/min) was injected into the source of the mass spectrometer, without splitting. All MS experiments were carried out in the negative mode [M-H] −1 . Nitrogen was used as the nebulizing gas and helium as the damping gas. The ion source parameters were as follows: spray voltage 5.0 kV and capillary voltage and temperature of 90.0 V and 350 • C, respectively. Data were collected and processed using MS Workstation software (v 6.9). Samples were firstly analyzed in full scan mode acquired in the m/z range 50-2000. RAW 264.7 cells and porcine skin fibroblasts were seeded at 2 × 10 4 and 5 × 10 4 cells, respectively, in 96-well plates. The MTT assay was performed according to the manufacturer's recommendations. Briefly, the cells were incubated with 100 µL of the extract (0.6, 1.2, and 2.4 mg/mL) and controls (triton X-100 at 1% v/v and DMEM medium) for 24, 48, and 72 h at 37 • C and 5% CO 2 . Thereafter, 10 µL of MTT (1% w/v) was added to each well and the plates were incubated for 2 h. Then, 100 µL of 2-propanol was added and the absorbance (abs) was read at 560 nm in a spectrophotometer (Sinergy HTX, Fisher Scientific, Waltham, MA, USA). The percentage of viability was calculated according to Equation (1) Cell proliferation was determined in RAW 264.7 cells and porcine skin fibroblasts stained with rhodamine B and fluorescein, respectively. Briefly, 1 mL of the extract (0.6, 1.2, and 2.4 mg/mL) and 1 mL of RAW 264.7 or fibroblast cell suspension (2 × 10 5 cells/mL) were mixed and incubated at 37 • C and 5% CO 2 for 48 h. DMEM was used as the control and Triton X-100 (1% v/v) as a positive control. The cells were then incubated with fluorescent dyes for two hours and transferred to a microscope slide. The fluorescence signal was observed with a fluorescence microscope (VELAB VE-146YT, Pharr, TX, USA). The samples were excited with a green laser for rhodamine (λ = 532 nm) and fluorescein (λ = 427 nm). Ten fields were randomly recorded for each slide and the assays were performed in triplicate. Fluorescence intensity was quantified using freely available ImageJ software (https:// imagej.nih.gov/ij/download.html accessed on 3 February 2023).
3.11. Effect of Extract on Cytokine Release from RAW 264.7 Cells RAW 264.7 cells were seeded at 5 × 10 4 cells in Eppendorf tubes. Cells were stimulated with bacterial lipopolysaccharides (LPS, 1 µg/mL) followed by the E. hyemale extract at 0.6, 1.2, and 2.4 mg/mL or control. Cell incubation was performed at 37 • C in 5% CO 2 for 24 and 72 h. At the end of the incubation, the supernatants were collected and frozen at −80 • C until use. Quantification of interleukin-10 (IL-10), tumor necrosis factor-alpha (TNFα), transforming growth factor-beta1 (TGF-β1), and monocyte chemoattractant protein-1 (MCP-1) was performed by immunoassay following the manufacturer's instructions.

Evaluation of Antimicrobial Activity of E. hyemale Extract
The antimicrobial activity of E. hyemale extract was evaluated by the broth dilution method. Briefly, a 0.5 McFarland standard was prepared with 0.5 mL of 1.175 w/v barium chloride dihydrate solution and 9.5 mL of a 1% v/v sulfuric acid solution (0.18 mol/L, 0.36 N). The optical density of the turbidity standard was then measured using a spectrophotometer (Metash Instruments Co. Ltd, Shangai, China) with a 1 cm cuvette at a wavelength of 600 nm, and bacterial suspensions of 1.5 × 10 8 CFU/mL were prepared. An aliquot of the suspension of S. aureus and E. coli strains was transferred to screw-capped glass tubes containing Müller-Hinton culture broth plus 1 mL of E. hyemale extract (0.12-48 mg/mL), resulting in a final concentration of 3 × 10 6 CFU/mL. The mixture was then incubated at 37 • C with continuous shaking. Samples were read at 600 nm after 48 h of incubation. Ceftriaxone was used as a positive control. Experiments were carried out in triplicate. The minimum inhibitory concentration (MIC) is defined as the lowest concentration of an antimicrobial agent that inhibits visible growth of a microorganism. MIC values were generated from non-linear fitted curves (growth inhibition versus log of concentration) using Equation (2) (Gompertz function) [83].
where M is the log concentration of the inflection point and B is a slope parameter.

Wound-Healing Effect of E. hyemale Extract in Type 2 Diabetic Rats
The present protocol was reviewed and approved by the Ethics Committee of the Autonomous University of Coahuila (TD-01-09-21-1). Rats were obtained from the biotherium Morelos. All animals received appropriate care according to the animal welfare guidelines established by the Mexican regulation NOM-062-ZOO-1999 and the Guide for the Care and Use of Laboratory Animals in the USA. Rats were housed in a temperatureand humidity-controlled rooms in our animal facilities with a 12 h light/dark cycle. Rats were allowed to acclimate for one week prior to the start of the study. Thirty male Wistar rats weighing 250-300 g (10-12 weeks old) were used. Throughout the study, rats had free access to standard rat chow and tap water ad libitum.
Type 2 diabetes was induced by a single intraperitoneal (i.p.) injection of nicotinamide (150 mg/kg). Fifteen minutes later, the animals received an injection of streptozotocin (STZ; 65 mg/kg, i.p.), as reported [84]. STZ was dissolved in 0.1 M citrate buffer (pH 4). Only rats with glucose levels above 200 mg/dL were included. Glucose levels were measured using a glucometer (Accu-Chek) and a drop of blood from the rats' tail.
The diabetic rats were anesthetized with pentobarbital (60 mg/kg, i.p.). After anesthesia, the back of the rats was shaved with an electric clipper. A round wound was then made on the back of each rat using a sterilized 10 mm biopsy punch. The rats were randomly divided into three groups: (1) non-diabetic control group (n = 6), injected with citrate buffer only; (2) type 2 diabetic control group (n = 6), both treated daily with physiological saline (0.9% v/v); and (3) type 2 diabetic groups treated daily with the extract (0.6, 1.2, and 2.4 mg/mL, n = 6 each). Wound size was recorded by camera and caliper at 0, 3, 7, 11, 14, 17, and 21 days. The percentage of wound contraction was calculated from the initial wound size using Equation (3): % wound contraction = Initial wound area − specific day wound area Initial wound area × 100 (3) 3.14. Histological Analysis Complete healing was observed at 21, 28, 24, 14, and 21 days in non-diabetic rats, type 2 diabetic rats, and type 2 diabetic rats treated with the extract (0.6, 1.2, and 2.4 mg/mL), respectively. The rats (n = 6 per group) were then anesthetized with pentobarbital (60 mg/kg, i.p.) and the healed dorsal skin was removed and placed in neutral buffered 4% v/v formalin for 24 h. Skin samples were dehydrated in ethanol and embedded in paraffin. Paraffin blocks were sectioned on a rotary microtome to obtain 5 µm skin cross sections and stained with Masson's trichrome kit according to the supplier's recommendation (Hycel, Guadalajara, JAL, Mexico) to measure collagen deposition. Tissue visualization was performed using an optical microscope. Collagen deposition was quantified using ImageJ software [85].

Statistical Analysis
Phenolic and flavonoid concentrations are expressed as mean ± standard deviation, whereas biological data are expressed as mean ± standard error of the mean (SEM). Differences in cell viability, proliferation, cytokine release, and collagen deposition were evaluated using the Tukey test after one-way or two-way analysis of variance (ANOVA) of repeated measures (wound healing data) was performed. Statistical significance was accepted at p < 0.05. All statistical analyses were performed with GraphPad Prism v8.0.

Conclusions
Ultrasound-and microwave-assisted extraction can be used to obtain minerals such as potassium, calcium, and silicon; sterols such as campesterol, γ-sitosterol, and cycloartenol; phenolic acids such as caffeic acid 4-O-glucoside and ferulic acid 4-O-glucoside; flavonols such as kaempferol 3,7,4'-O-triglucoside, kaempferol 3,7-O-diglucoside, and quercetin; a phenylpropanoid such as phenol-2,4-bis(1-phenylethyl); and a lignan such as conidendrin from the Mexican E. hyemale plant. This is the first time that both phenol-2,4-bis(1phenylethyl) and conidendrin have been identified in this plant. The extract obtained by this technique has a crystalline structure with a high presence of polar groups and shows resistance to thermal degradation. Its pharmacological properties include antimicrobial effects against S. aureus and E. coli, control of inflammation by increasing IL-10 and inhibiting MCP-1 released by macrophages, and promotion of collagen synthesis by dermal fibroblasts. It is highly likely that its anti-inflammatory and collagen-synthesizing effects benefited to faster wound healing in diabetic rats. Institutional Review Board Statement: The animal study protocol was approved by the Ethics Committee of the Autonomous University of Coahuila (protocol code TD-01-09-21-1 approved on 13 September 2021).

Informed Consent Statement: Not applicable.
Data Availability Statement: The data presented in this study are available upon request from the corresponding author.